- Open Access
Long noncoding RNAs in lipid metabolism: literature review and conservation analysis across species
BMC Genomics volume 20, Article number: 882 (2019)
Lipids are important for the cell and organism life since they are major components of membranes, energy reserves and are also signal molecules. The main organs for the energy synthesis and storage are the liver and adipose tissue, both in humans and in more distant species such as chicken. Long noncoding RNAs (lncRNAs) are known to be involved in many biological processes including lipid metabolism.
In this context, this paper provides the most exhaustive list of lncRNAs involved in lipid metabolism with 60 genes identified after an in-depth analysis of the bibliography, while all “review” type articles list a total of 27 genes. These 60 lncRNAs are mainly described in human or mice and only a few of them have a precise described mode-of-action. Because these genes are still named in a non-standard way making such a study tedious, we propose a standard name for this list according to the rules dictated by the HUGO consortium. Moreover, we identified about 10% of lncRNAs which are conserved between mammals and chicken and 2% between mammals and fishes. Finally, we demonstrated that two lncRNA were wrongly considered as lncRNAs in the literature since they are 3′ extensions of the closest coding gene.
Such a lncRNAs catalogue can participate to the understanding of the lipid metabolism regulators; it can be useful to better understand the genetic regulation of some human diseases (obesity, hepatic steatosis) or traits of economic interest in livestock species (meat quality, carcass composition). We have no doubt that this first set will be rapidly enriched in coming years.
Lipids are found in all organisms and are essential for life [1,2,3]. They contribute to cell membrane constitution, acting as signaling molecules and as an important source of energy. In animal species, the deregulation of lipid homeostasis processes is responsible for dyslipidemia and many diseases of major importance in human health such as obesity, diabetes, non-alcoholic fatty liver disease (NAFLD) or cardiovascular diseases. The major site of lipid synthesis may differ from one species to another. Lipogenesis from carbohydrates sources occurs mainly in the liver in primates and rodents, and in adipose tissue in carnivores and ungulates (pig, cow, goat, dog) . Note that for chicken [4,5,6] and many fishes , the major site of de novo fatty acid synthesis is the liver. The synthesis of cholesterol in mammals, birds and fish is more ubiquitous but predominates in the liver [5, 8,9,10]. The storage of fatty acids in triglycerides is the main animal’s energy reserve, which is constituted during periods of energy excess and mobilized during periods of energy deprivation. This storage mainly occurs in adipose tissue within the adipocytes. Energy homeostasis is regulated by hypothalamus which regulates food intake and energy expenditure , and involves many hormones and adipokines to organize the crosstalk between organs. Lipid metabolism is a complex process that involves a large variety of molecular pathways and different transcriptional regulators some of which have been described so far.
Since the 2000s, with the advent of whole-genome sequencing technologies, most genes coding essentially for proteins have gradually been identified. The databases reference nearly 20,000 genes in human  [Human GENCODE v.28–10 July 2018], 22,000 in mouse  [Mouse GENCODE v.M17–10 July 2018] and pig [Ensembl v.92–10 July 2018], 18,000 in chicken [Ensembl v.92–10 July 2018]. Small RNAs, such as miRNA that do not code for proteins, are also relatively well annotated today (from 1705 to 5531). In contrast, long noncoding RNA (lncRNA) are less described in the genomes: they are strictly defined as RNAs of more than 200 nt with no ORF long enough to be translated into a protein (< 150 nt) . They have important roles since they control the regulation of gene expression via a large diversity of mechanisms as they can interact with DNA, RNA or proteins [15, 16]. The number of lncRNAs with a well-described functional role is now estimated at 1% . lncRNA genes appear to be as numerous as or even more numerous than genes encoding proteins with 15,779 and 12,533 lncRNA referenced via the GENCODE projects [12,13,14] in human [Human GENCODE v.28] and mouse [Mouse GENCODE v.M17], respectively. Modeling of these gene entities structure is far from complete. In human, specialized databases such as NONCODE  or LNCipedia  announce even higher numbers than those referenced in Ensembl and NCBI databases. On the contrary, in less studied livestock species such as pig and chicken [Ensembl v.92], a very small fraction of lncRNA is referenced (361 and 4643, respectively). So far, most lncRNA and their underlying transcripts, are gene models predicted by bioinformatics pipelines from RNAseq data and in the majority of species have rarely been experimentally confirmed. The difficulty of lncRNA gene modeling and identification is due to different causes: 1. an expression 10 to 100 times weaker than the protein coding genes [14, 20, 21], which makes harder the identification of the different transcripts exon-intron structures and therefore of the gene locus; 2. the tissue-specificity of lncRNA expression [14, 20], requiring the use of many different tissues to establish an exhaustive catalogue; 3. the criteria used for lncRNA prediction that can be the presence of an ORF, a blast against a protein database, the size of transcripts and/or the composition in k-mers, depending on the bioinformatics tool used; the main tools being CPC [22, 23], CPAT , PhyloCSF , FEELnc  and the Ulitsky’s team pipeline PLAR . 4. Finally, a last point concerns the low conservation of lncRNA sequences between species, especially for species that are evolutionary distant [14, 20, 27,28,29,30]. All these drawbacks make it difficult to find orthologous long noncoding genes by sequence conservation analysis, as frequently done for protein-coding genes.
The first review about lncRNAs involved in lipid metabolism is very recent  (2016). Since then several other reviews and articles were published but none of them provided an exhaustive lipid-related lncRNA catalogue. The first objective of this study was to fill this gap providing an exhaustive catalogue of lncRNAs involved in lipid metabolism. An extensive analysis of the literature, generally focusing on human or mouse, allowed us to draw up a catalogue of 60 lncRNA genes related to lipid metabolism for which we report mechanisms of action when it is described This led us to highlight some spurious genes and therefore, to rename some lncRNAs in accordance to the rules published by the HUGO Gene Nomenclature Committee for long noncoding genes . Second, we analyzed the conservation of these 60 lncRNA in chicken, which last shared common ancestor with mammal dates back to 300 M years ago, with the assumption that such a conservation would support an important role of these genes in the metabolism of interest. For this, an approach by synteny analysis was used, which highlighted 5 lncRNAs preserved between human/mouse and chicken. Finally, we have more precisely described their functional roles and analyzed their conservation between 8 species from mammals to zebrafish.
60 lncRNA identified as involved in lipid metabolism by expert curation of the literature
To our knowledge, the first catalogue of lncRNA potentially involved in lipid metabolism was proposed by Chen in 2016  and included the 5 lncRNA, called lncLSTR, HULC, APOA1-AS, lincRNA-DYNLRB2–2 and SRA. The same year, Zhou et al.  published a broader review of lncRNA genes potentially involved in lipid and glucose metabolisms and related diseases (atherosclerosis, type 2 diabetes, insulin resistance) in which TRIBAL, ANRIL, lncLSTR, AT102202, APOA1-AS, lincRNA-DYNLRB2–2, RP5-833A20.1 and CRNDE were described as involved in lipid metabolism. Later in the year, Smekalova et al.  published a list of lncRNA involved in liver pathophysiology including two lncRNA involved in lipid metabolism HULC and lincRNA-DYNLRB2–2 and Ananthanarayanan  reports three other lncRNAs involved in triglyceride, cholesterol and bile acid homeostasis: lnc-HC, lncLSTR, APOA1-AS. In 2017, Zhao et al.  present a review on lncRNA involved in liver metabolism and cholestatic liver disease in which lncLSTR, Lnc18q22.2, SRA1, HULC, MALAT1, lncHR1 were related to the lipid metabolism and lnc-HC, APOA1-AS, H19, MEG3, lincRNA-DYNLRB2–2, LeXis involved in cholestatic liver pathologies. More recently, in 2018, Van Solingen et al.  present a review covering the 12 lncRNA previously described by Zhao et al. enriched with RP5-833A20.1 renamed NFIA-AS1 and MeXis a new lncRNA discovered in early 2018 by the team of Tontonoz . Likewise recently, Zeng et al.  added eight other lncRNAs: Gm16551, SPRY4-IT1, APOA4-AS, LINK-A, RP1-13D10.2, E330013P06 (named CARMN in databases), LOC100506036 (named CNNM3-DT in databases) and SNHG14. All these reviews report a total of 27 lncRNA involved in lipid metabolism. An extensive literature analysis allowed us to add 33 new lncRNAs, bringing the total to 60 lncRNAs. These extra lncRNAs include one identified in 2015 not mentioned in the aforementioned studies, it was the lncRNA AT115872 described with the lncRNA AT102202 (more largely cited in the literature). The first acts at distance on the expression of ACAT2, that encodes a key enzyme for the absorption of dietary cholesterol, while the second acts locally on the HMGCR gene, which encodes a key enzyme for cholesterol anabolism . Other genes have been described between 2016 and today: 8 in 2016, 15 in 2017 and 15 in 2018. These 60 genes potentially involved in lipid metabolism are listed in Table 1. Most of these genes have been identified in human (34) and mouse (19) with two in both species, the others have been described in rat (1) or livestock species as pig (5) and chicken (4).
Mechanisms of action of lncRNAs
The demonstration of a link between the lncRNA of interest and lipid metabolism can be variable from a publication to another (Table 1). For 38 of the 60 genes, a direct or indirect causative effect of the lncRNA on the lipid metabolism is given in response to an invalidation and/or an overexpression of the lncRNA. Such experiments were conducted in human (22) or murine (4) cell cultures or through in vivo experiments, by injection of viral vector in the tail of mice (11) or more rarely KO mice (3 with LeXis, MeXis and SRA1 lncRNAs). Out of these 38 studies, 25 go further to partially or totally decipher the action mechanism (Table 2). For 20 of the 60 genes, the link with lipid metabolism was only based on a co-expression between the lncRNA and one (several) transcript(s) or metabolite(s) related to the lipids in response to a disease (10), a genotype (6) or a molecule (8) known to act more or less specifically on lipid metabolism. Finally, 3 studies reported a link with lipid metabolism by GWAS analysis between genetic markers within or close to the lncRNA and a phenotype associated to lipid metabolism suggesting that the lncRNA is a potential causal gene for the phenotype variation.
All the 60 lncRNAs we suggested as involved in lipid metabolism cover most of the types of action described so far in the literature for the noncoding genes. As shown in Fig. 1, these lncRNAs may function as regulators of the transcription by acting at the DNA level (Fig. 1a), of the post-transcription and translation by acting at the RNA level (Fig. 1b) and finally of the post-translation by acting at the protein level (Fig. 1c). Concerning the underlying biochemical mechanisms, most of them are based on lncRNA-RNA or lncRNA-protein(s) interactions. RNA immunoprecipitation and pull-down assays  have revealed a vast range of interactions between lncRNAs and proteins, proteins that sometimes interact with other RNAs. Such interactions constitute real scaffolds that can inhibit or activate different biological processes. At the transcriptional level (Fig. 1a), different studies showed an action of lncRNAs on the promoters of genes involved in lipid metabolism. For example, it is the case of LeXis as reported in a very comprehensive study conducted by the Tontonoz’s lab  (Fig. 1a, right part): first, LeXis was observed as the most up-regulated lncRNA in mouse primary hepatocytes when treated with GW3965, an agonist to the liver X receptor (LXR) that mediates cellular and systemic cholesterol homeostasis and in particular inhibits cholesterol biosynthesis. The existence of a response element to LXR was then demonstrated in the LeXis promoter using luciferase reporter gene experiment and ChIP-qPCR. Using overexpression of LeXis by adenovirus injection or knockdown experiments in mouse, the authors show that LeXis decreased cholesterol and HDL and decreased the expression of genes involved in the cholesterol biosynthesis pathway. LeXis−/− mice also showed an increase in hepatic cholesterol. Present in the nucleus, LeXis is suspected to interact on gene transcription by modifying protein recruitment on chromatin. Tontonoz’s lab then demonstrates, using ChIRP/SM and ChIP experiments, a binding of LeXis on the heterogeneous nuclear ribonucleoproteins (hnRNP) RALY, suspected to be a potential transcriptional co-factor. Its knockdown is responsible for a decrease in cholesterol levels as well as genic expression in cholesterol biosynthetic pathway. The authors show, using knockdown and ChIP-qPCR experiments that RALY binds the promoter of different cholesterologenic genes and activates their expression, activation affected by LeXis through the modulation of RALY DNA-binding .
Other studies have shown an action of lncRNAs on the transcription. For example, APOA1-AS seems to inhibit the transcription of the APO gene cluster (APOA1, APOC3, APOA4, APOA5) that codes for protein components of lipoproteins, by DNA compaction through epigenetics mark modulation  (Fig. 1a, left part). This mechanism seems to require the recruitment of the LSD1 protein known to induce gene silencing through the removal of active methyl marks, and of the SUZ12 protein, a key component of the polycomb recessive complex (PRC2) known to mediate chromatin silencing through H3K27 trimethylation . Indeed, the APOA1-AS depletion in HepG2 cells increased the active histone H3K4me3 marks at the APOA1 promoter in parallel to a significant decrease of LSD1 occupancy. APOA1-AS depletion also decreased the repressive histone H3K27me3 marks at the APOA1 promoter that coincided with a marked reduction of SUZ12 occupancy in this region . A second example of lncRNA action on DNA compaction is Lnc-leptin  (Fig. 1a, middle part). By using chromatin conformation capture experiments, a direct interaction was detected between lnc-leptin and the LEP (leptin) gene, which codes for a major adipokine secreted by white adipocytes and functioning as an energy sensor to regulate energy homeostasis. This “lnc-leptin – leptin promoter” interaction occurred at the enhancer region of LEP and it was diminished upon lnc-leptin knockdown in mature adipocytes.
At the post-transcriptional level, some lncRNAs seem to play a role in the maturation of RNAs such as lncRNA uc.372 (Fig. 1b, left part) which prevents the maturation of a pri-miRNA by camouflaging the area targeted by the Drosha protein . On mature RNAs, the so called “competing endogenous RNA (ceRNA)” role of lncRNAs resembles that of a sponge for small RNAs regulating the mRNA target of small RNAs (Fig. 1b, middle part). Among the lncRNAs involved in lipid metabolism, NEAT1 , SNHG16  and PVT1  are endogenous competitors of ATGL, SCD and FASN transcripts, respectively. Sometimes, lncRNA-protein complexes target a mRNA and thus regulate its stability (lnc-HC , H19 , MEG3 , NEAT1 , APOA4-AS ) or its translation (lncSHGL ) (Fig. 1b, right part). LncRNAs can bind via their three-dimensional conformation, involving one or more proteins in the structure (Fig. 1c). They can bind via their sequence RNA of hnRNP such as SPRY4-IT1  (Fig. 1c, left part). They can also form protein scaffolds such as Blnc1 which associates with EDF1, LXRα and hnRNPU  or linc-ADAL which associates with IGF2BP2 and hnRNPU  (Fig. 1c, left part). These protein scaffolds do not yet have a well-defined mechanism of action. Some publications have gone further by highlighting the interest of this complex. For example, lncRNA protein complexes can modulate the half-life of the proteins involved in the complex, such as MALAT1 which binds to SREBP1c in order to stabilize it  (Fig. 1c, middle part), or they can modulate its function, such as LINK-A which binds to PIP3 and intensifies its interaction with Akt  (Fig. 1c, right part) or modify its cell location as illustrated by NRON . Another role of lncRNA  is that of hosting small RNAs (Fig. 1d). SNHG16  illustrates very well this role because it hosts 3 small nucleolar RNAs (snoRNA) SNORD1A, SNORD1B and SNORD1C which are positioned within the introns in the sense direction of the lncRNA, thus benefiting from the co-transcription with the host lncRNA. Finally, lncRNAs can also host small ORFs (Fig. 1e) allowing the translation of small peptides. CASIMO1 is a perfect example, lncRNA CASIMO1 hosts the sequence of a small transmembrane peptide that interacts directly with the SQLE protein and modulates the formation of lipid droplets .
New names proposed for misnamed lncRNAs
When a new field is explored, the associated nomenclature requires a certain amount of time to be standardized; this was the case for the nomenclature associated with protein-coding genes and of course it is also the case for the long noncoding genes. When referring to the official HUGO gene nomenclature committee (HGNC), it appears that some lncRNA were not properly named, which can lead to misunderstandings. Indeed, the HGNC lists very precise rules on how to name lncRNA . These can be summarized in seven points (Fig. 2): 1. if the lncRNA function is well described, the lncRNA takes an abbreviated name symbolizing its function, e.g. LeXis for liver-expressed LXR-induced sequence, lncLSTR for liver-specific triglyceride regulator. In the case of unknown function, the lncRNA takes the symbol gene name of the gene harboring it enriched by a suffix describing its genomic location: 2. the ‘Intronic’ and ‘sense’ lncRNA genes are appended with -IT for Intronic Transcript (e.g. SPRY4-IT1); 3. the ‘sense’ and overlapping a protein-coding gene lncRNA gene are appended with the suffix -OT for Overlapping Transcript (e.g. SOD2-OT1); 4. the ‘Antisense’ lncRNA gene are appended with the suffix -AS for Antisense (e.g. APOA1-AS, NFIA-AS1). 5. Close intergenic divergent lncRNA (< 1 kb) transcribed in the opposite direction to nearby protein-coding genes takes the gene symbol name appended with the suffix -DT for Divergent Transcript (e.g. DHCR24-DT). 6. Other intergenic lncRNAs take the name LINC followed by a number assigned by HGNC committee (for human genes). 7. An exception exists for lncRNAs hosting small noncoding RNAs that take the name of the small hosted RNA appended with the suffix HG for Host Gene (e.g. SNHG16). Finally a long noncoding transcript that has common splice junctions with protein-coding transcripts is considered as an additional isoform and therefore belongs to this protein-coding gene . In spite of this approved nomenclature guidance, some lncRNAs are still misnamed. For example the lncRNAs described by Tristán-Flores et al.  have been misnamed in lncACACA, lncFASN and lncSREBF1, although they are neither sense nor antisense of the ACACA, FASN and SREBP1 genes. The lncRNA depletion by KO experiments affected the expression levels of the three genes, which again does not allow to use these names.
We propose to rename some lncRNAs according to the HGNC rules whatever the species (Table 1, column 3). Seven lncRNA have been renamed according to the nearby protein-coding gene: lnc_DHCR24  in DHCR24-DT, AT115872  in SOD2-OT1, XLOC_014379  in NF1-IT1, FLRL3  in RAD54B-AS1, XLOC_019518  in RNF7-DT. We have also renamed two other genes: LISPR1 (long intergenic noncoding RNA antisense to S1PR1)  in S1PR1-DT, and uc.372 (ultra-conserved 372)  which has a generic name and should be rather called RALGAPA1-AS1. We have restored the official and standardized names, LINC01970 and SMCR2 (Smith-Magenis syndrome Chromosome Region, candidate 2), for the two lncFASN and lncSREBF1 genes  respectively. All other XLOC_013639, XLOC_011279, XLOC_064871 , lncACACA , LOC157273 , Gm16551 , PLA2G1Bat1  and lnc-KDM5D-4  genes should have a standard name of the type LINC#####. Finally, the lncRNA AT102202 has several common splice junctions with the HMGCR protein-coding gene and should therefore be considered as a HMGCR isoform rather than a lncRNA new gene. Note that the knockdown of this isoform in HepG2 cells was described by Liu et al. to increase the expression level of the gene encoding HMGCR due to the presence of several HMGCR isoforms with different expression patterns ; although the authors missed to specify which isoform was targeted by siRNAs and which one was up-regulated (see Additional file 1). According to this figure, the knockdown of the AT102202 isoform should lead to an absence of HMGCR functional protein.
In some cases, a gene is named with several aliases between species. This is the case for lncSHGL in mouse known as B4GALT1-AS1 in human which were both mentioned in Wang et al. . Naming problems also exist within the same species. For example, the NCBI mouse gene named Gm30838 by the MGI (Mouse Genome Informatics), is double named in Lo et al. lnc-ORIA9 and lnc-leptin . Similarly, the human ENSG00000266304 lincRNA gene, firstly known as RP11-484 N16.1, was named lnc18q22.2 by Atanasovska et al.  and finally officially renamed LIVAR. Due to their recent studies, we found some genes in databases with an “ID” name instead of its common names used in the literature (e.g. AC023161.1 instead of lncHR1 ). Other problems are due to some articles that use lncRNA gene names without referring to any database: the most classical examples are XLOC/TCONS names reflecting experiment-dependent naming from Cufflinks (e.g. pig new genes in Huang et al. ) but other names exist such as AT102202  which does not refer to any easily detectable source because it is a contraction of the NONCODE ID NONHSAT102202.
Detailed examination of model architecture
It is important to note that the vast majority of RNAs present in the databases are only predictions and that their structure has only very rarely been validated experimentally. A lncRNA model localized close to a protein-coding gene and in a same strand of this latter can be spurious; it is possible to be an extension of the protein-coding gene due to the difficulty of modelling the ends of transcripts . We detected two lncRNA in this case. The ALDBGALG0000005049 lncRNA is close (~ 1 kb from the SCD 3’UTR) and on the same strand of the SCD gene (Fig. 3a), that encodes the stearoyl-CoA desaturase enzyme that catalyzes the rate-limiting step in the formation of monounsaturated fatty acids. Fan et al. described in chicken myoblasts that the inactivation of the ALDBGALG0000005049 gene by siRNA led to an under-expression of the SCD gene and a modulation of other genes such as PPARA, PPARB and PPARG (Peroxisome Proliferator Activated Receptor)  making this lncRNA a potentially important lncRNA in lipid metabolism. However, we propose here to verify the existence of the ALDBGALG0000005049 gene using chicken liver cDNA treated by DNAse using genomic DNA as control. The amplification of the intergenic region “SCD-ALDBGALG0000005049”, confirmed by sequencing, clearly shows the existence of a transcript that overlaps the two genes (Fig. 3b), demonstrating that ALDBGALG0000005049 and SCD are in fact a single gene (Fig. 3c). We report another case, the lncRNA FLRL7, located very close (150 nt from the FADS2 3’UTR) and on the same strand of the FADS2 (fatty acid desaturase 2) protein-coding gene (Fig. 3d) and whose expressions were both up-regulated in the liver of NAFLD mouse according to Chen et al. . We demonstrated using mouse liver cDNA treated by DNAse that FLRL7 and FADS2 genes are a unique gene (Fig. 3e), thus extending the 3′ UTR end of the FADS2 gene (Fig. 3f).
Conservation between phylogenetically distant species
Gene conservation during evolution, especially between phylogenetically distant species suggests an important functional role for these genes. Conservation of function of lncRNA across species was tested in some studies, showing a function retained despite a minor sequences conservation . However the task remains difficult because of the poor conservation of lncRNA sequences between phylogenetically distant species as opposed to protein-coding genes, suggesting a more rapid evolution of lncRNA during evolution [14, 20, 27]. Therefore, we propose here to carry out orthologous lncRNA searches between phylogenetically distant species (chicken and mammals) using an approach based on the genome synteny as already presented in Muret et al.  and Foissac et al.  (see Materials & Methods). Even if this manual approach is time-consuming, we investigated the whole 60 long noncoding genes involved in lipid metabolism.
Out of the 60 lncRNA genes mentioned in the Table 1, five genes satisfy the aforementioned criteria between chicken and man (or mouse) and can therefore be considered as orthologous between the species analyzed: there are CRNDE, DHCR24-DT, NFIA-AS1, PVT1 and SRA1. Their roles are described in more detail below. We can note that 5 other lncRNAs are potentially orthologous since 1. they correspond positionally to several lncRNAs in the other species or 2. the gene environment has slightly evolved, e.g. a new coding gene appear in locus or the distance between genes are different between species. These lncRNAs are lncACACA, DYNLRB2–2, MeXis, PLA2G1Bat1 and TRIBAL. Table 3 shows the genomic positions in human, mouse and chicken of these 10 lncRNA. These lncRNAs potentially play important roles in lipid metabolism since they act on the expression of key genes of this metabolism as key enzyme genes (FASN, SCD, ACADS, ACADVL, ATGL), lipid transport genes (ABCA1, FABP4) or lipid metabolism transcription factor genes (PPARA, PPARG).
CRNDE (ColoRectal Neoplasia Differentially Expressed) is a lncRNA divergent with respect to the IRX5 gene, at 2 kb and 1.2 kb in human and chicken, respectively. In chicken, it has been described as ORat7  (ALDBGALT0000001763). Composed of 6 to 9 exons in chicken and 6 exons in human, CRNDE is mainly noncoding but some isoforms are known in human to code for small proteins . In human, CRNDE knockdown by siRNA in colorectal cancer cell lines leads to an under-expression of FASN, and an overexpression of ACADVL and ACOT9, two genes involved in lipid catabolism .
Lnc_DHCR24, renamed in DHCR24-DT (Table 1), is a lncRNA divergent with respect to the DHCR24 gene coding for a key enzyme of the cholesterol synthesis. We have modelled this transcript for the first time in 2017 in chicken and located a possible orthologue in human . The intergenic region is very small, i.e., 200 bp in human and 300 bp in chicken . In a previous study, we have suggested that these two genes are likely to be co-regulated by a bi-directional promoter, because of their high hepatic co-expression in several chicken lines (layers and broilers) analysed at different ages (young and, adult stage) .
NFIA-AS1 is an intronic antisense lncRNA of the NFIA gene (Nuclear Factor I A). Composed of 4 to 7 exons, it is found on the second intron of NFIA gene in human as well as in chicken. It negatively regulates in THP-1 cells the expression of the NFIA gene by a negative feedback mechanism with the transcription factor NF1A binding the promoter of NFIA-AS1 to activate it . LncRNA NFIA-AS1 (also called RP5-833A20.1) is induced by a high level of oxidized and acetylated LDL . These two genes (NFIA-AS1 and NFIA) appear to regulate the homeostasis of cholesterol (LDL, HDL, VLDL) and inflammatory cytokines (IL-1β/6, TNF-α and CRP) in Apo−/− mice .
PVT1 (Plasmacytoma Variant Translocation 1) is a same strand lncRNA with respect to the MYC nearest protein-coding gene. Modelled in the NCBI databases of human, mouse and rat, the two genes are separated by 50-60 kb in these three species. In the chicken, we also found it at the same distance (56 kb) of the MYC gene. PVT1 in human is a competitive endogenous lncRNA by acting as a sponge of MIR-195 in osteosarcoma cells . It upregulates BCL1 and BCL2, two genes playing roles in the control of cell cycle and apoptosis, but also FASN, one of the key lipogenic enzymes.
SRA1, better known by its first name SRA (Steroid Receptor Activator), is one of the first lncRNA described in human (1999) . Its functional RNA acts as a steroid receptor coactivator. It can coactivate androgen receptor (AR), estrogen receptors (ERα, ERβ), progesterone receptor (PR), glucocorticoid receptor (GR), thyroid hormone receptor (TR) and retinoic acid receptor (RAR) . As early as 2003, it was demonstrated that its codes for a functional SRAP protein improving the trans-activation of PPARG and genes coding for AR and GR . In Human, as in mouse or other species, this double “protein coding-lncRNA” classification exists . In this review, we are only interested in its noncoding isoform. SRA1 is an antisense exonic lncRNA of the gene coding for ANKHD1 in human. Currently, we do not know if SRA1 has noncoding isoforms in chicken but a coding isoform is present in Ensembl database (ENSGALG00000040453). Using a mouse SRA1 KO, the noncoding SRA1 isoform seems to regulate in the liver the expression of genes involved in lipid metabolism as PPARA, PPARG, FABP4 and SCD by a mechanism still unknown . In 2016, the same team showed that in liver, the noncoding SRA1 isoform positively regulates the expression of PNPLA2. PNPLA2 codes for an enzyme that plays a role in lipid hydrolysis that if under expressed leads to the progressive fatty liver steatosis .
For the previous 5 lncRNA found to be preserved between human and chicken, two model species, xenope and zebrafish, and three livestock species, goat, bovine and pig, have been added to the syntenic conservation analysis to better appreciate the conservation in vertebrates. Note that the model species xenope (370Myr) and zebrafish (440Myr) are more phylogenetically distant from human than the chicken (320Myr) (Fig. 4a). We have selected also cattle and pig because they are economically important livestock species, widely consumed in the world. To study conservation, in addition to the public reference Ensembl and NCBI databases, we used the lncRNA catalogues that we recently published for these species . The Fig. 4b shows the conservation of the 5 lncRNA across the 8 species. In the current state of the genome annotation, two genes DHCR24-DT and NFIA-AS1 are preserved only within some amniotes, despite the fact that the two DHCR24 and NFIA neighboring protein-coding genes were conserved in other vertebrates. Such observations can be due to a poor gene annotation in the species were these two long noncoding genes were not identified. Another hypothesis is a convergent evolution in mammals and birds that could explain why it is present in chicken and not in other mammals that are evolutionary closer to human and mouse. On the other hand, CRNDE is found in all tetrapods with robust reliability and the cluster of IRX genes in which CRNDE is located is very strongly preserved in vertebrates . Finally, two genes are conserved in all vertebrates: PVT1 and SRA1 which are in particular involved in FA biosynthesis through the regulation of two key enzymes FASN and SCD respectively.
We then studied the expression of these five lncRNA in three tissues known to be involved in lipid metabolism, using human  and chicken samples. The tissues chosen were the liver and adipose tissue as key organs/tissues for lipid synthesis and triglyceride storage. The third tissue is the hypothalamus because of its central role in energy homeostasis via the regulation of food intake and energy expenditure . The chicken embryo was also studied because many lncRNAs were described as expressed during embryonic development [111,112,113]. The expression of the 5 lncRNAs is shown in Fig. 5a. In chicken the 5 lncRNAs were overexpressed in the 3 tissues and in the embryo compared to the total lncRNA expressions (t-test; p-value < 0.05), the median of their expression being equivalent to the third quartile of the total lncRNA expression (Fig. 5b). LncRNAs are known to be very poorly expressed compared to protein-coding genes (10 to 100 times less [14, 20]). This observation shows that the lncRNAs described so far are generally more expressed than the whole modelled lncRNAs. PVT1 and SRA1 were well expressed in all 3 tissues, both in human and chicken. DHCR24-DT was overexpressed in the liver of both species compared to the other tissues. On the contrary, CRNDE was not expressed in human, at least in the tissues and samples analyzed. Finally, NFIA-AS1 was not expressed in any of the 3 tissues analyzed, whatever the species. This does not preclude for expression in other tissues, because Hu et al. have shown a link between this gene and lipids in macrophage cells .
To our knowledge, previous reviews taken together described 27 lncRNAs involved in lipid metabolism. An extensive research has allowed us to report 33 additional lncRNAs, the majority of which identified in human or mouse, resulting in a total of 60 long noncoding genes having a role in lipid metabolism. Such a research has to be meticulous because of the multiple aliases intra and between species and is tedious and time-consuming.
In addition to gathering these 60 genes as related to the lipid metabolism, we demonstrated experimentally that two lncRNA close and on same strand with the SCD and FADS2 protein-coding genes and called by the authors as ALDBGALG00000000505049 and FLRL7 related to the lipid metabolism, were spurious. We also made a lncRNA nomenclature revision and propose to rename some genes according to the official rules of the HUGO gene nomenclature committee .
We then performed a comparative analysis to identify orthologous genes between phylogenetically distant species. Such a approach allows to make use of the knowledge obtained in one species to infer the presence on lncRNAs in other species not examined so far. In particular, it facilitates the understanding of the biological role by working on species in which gene manipulations are easier. Unfortunately, this research is difficult for lncRNAs because these genes are very poorly conserved in sequence between relatively distant species; such research required synteny approaches to study the conservation of the local genomic structure around the gene of interest. We identified, out of the 60 lncRNAs, 5 lncRNAs conserved within amniotes (320Myr), including two conserved within vertebrates (440Myr). Such results are consistent with other studies; some articles reported less than 20% of lncRNAs conserved across mammals [114, 115]. Interestingly, we showed that lncRNAs described so far are more expressed compared to the whole lncRNAs present in the gene databases; the reason is likely technical since it is easier to work on lncRNAs that are more expressed.
Such a catalogue of 60 genes is interesting, first, by providing new regulators of a complex lipid metabolism known to be highly regulated at the mRNA levels [42, 76]. Second, because the lipid metabolism is particularly important in human health through the numerous diseases related to this metabolism (obesity, cardiovascular diseases, hepatic steatosis ...). Third, because this metabolism is also important in livestock species where it is linked to economically important traits, such as intramuscular fat content, meat quality traits [116,117,118] and ectopic fat deposition and economic carcass values. It should be noted that more than 2/3 of the 60 lncRNAs reported in this review were discovered in the last 2 years and we have no doubt that this first set will be rapidly enriched in the coming years.
The state of the art regarding lncRNA potentially involved in lipid metabolism was obtained by expert curation of the literature database Pubmed. In this way, lipid metabolism was defined as the including synthesis, degradation and transport of different types of lipids, with a particular interest for fatty acids and cholesterol. The keyword literature search was therefore conducted by combining the terms “lncRNA” and one of the following terms associated to apolipoprotein or to the 8 lipid classes: sterol (cholesterol), prenol, fatty acid, acylglycerol (triglyceride), phosphoglyceride, glycolipids, polyketides and sphingolipids.
Syntenic conservation between the chicken and the species where the lncRNA was discovered
The syntenic conservation analysis was performed for all 60 lncRNA genes identified in the first step, using the following annotation reference databases: Ensembl v.92, NCBI release 109, NONCODEv5 , ALDB v1.0 , completed by the new lncRNA models that we have previously published for chicken [20, 28]. Long noncoding gene conservation by synteny analysis between human/mouse and chicken was performed according to three criteria used in the following order of priority: 1. the lncRNA in human/mouse genome is surrounded by two neighboring protein-coding genes for which a 1-to-1 orthologous gene is available in the chicken genome. We considered the lncRNA as syntenically conserved if this lncRNA was also found in chicken between these two orthologous protein-coding genes, in the same orientation and order and same relative position and/or intron-exon structure. 2. The lncRNA in human/mouse genome is a close divergent lncRNA (< 1 kb) or antisense from a protein-coding gene with a 1-to-1 orthologous gene in the chicken genome; 3. the lncRNA in human/mouse genome is hosting small noncoding genes. Such a lncRNA was syntenically conserved if a lncRNA in chicken is hosting small noncoding genes with the same numbered-names.
Syntenic conservation between eight species
The syntenic conservation analysis was further performed across eight species (human, mouse, goat, cattle, pig, chicken, xenope and zebrafish) for the subset of 5 lncRNA genes, which were found conserved between the chicken and the human/mouse. We used the same three criteria aforementioned, taking the lncRNA reference databases in the following order: Ensembl v.92, NCBI annotation release 109, and the new lncRNA catalogue that we have previously published for livestock species (goat, cattle, pig) . The phylogenetic tree was performed with the phyloT v2018.3 tool (https://phylot.biobyte.de/), which generates phylogenetic trees based on NCBI species names and taxonomy. The tree visualization was carried out with the iTOL v4.2.3 tool .
Tissue expression analysis in chicken and human
The human expression raw data from liver, white adipose tissue and brain were obtained from RNAseq data (2 × 100 bp) from three subjects (approximatively 18 M read-pairs per sample) chosen from the NCBI BioProject accession number PRJEB4337 . The aim of Fagerberg et al. was to study tissue-specific expression of genes from 27 healthy human tissues. The chicken liver and abdominal adipose tissue expression data were obtained from RNAseq data (2 × 100 bp) from 16 animals (about 55 M read-pairs per sample for liver and 70 M for adipose tissue) extracted from our PRJNA330615 project . The aim of Muret et al. was to model new lncRNA in chicken in these two tissues. For the hypothalamus and the embryo in chicken, the raw data used correspond to RNAseq data (2 × 150 bp) from 16 individuals (approximately 50 M read-pairs per sample - PRJEB28745). For these 2 species and all the tissues mentioned, normalized RPKM data were used.
RT-PCR for remodeling gene structure
Total RNAs was extracted from the liver of 48 chickens (from 9-weeks broilers) and mice (C57BL/6) as described by Desert et al.  and reverse-transcribed using High-Capacity cDNA Reverse Transcription kit (Applied Biosystems, Foster City, CA) following manufacturer’s instructions. cDNAs was treated with DNAseI (kit Ambion – RNAse-free) and diluted 1:10 for specific PCR amplification using the primers defined in Additional file 2. The amplification specificity was confirmed by sequencing. The amplification fragment lengths were verified on 2% agarose gel using the marker SmartLadder (Eurogentec MW1700_10).
Availability of data and materials
RNA-Seq data for chicken livers and adipose tissues are available on SRA at project PRJNA330615 and for chicken hypothalamus and embryos on ENA at project PRJEB28745.
Human nasopharyngeal carcinoma cell line
ATP-Binding Cassette A1/G5
Acetyl-CoA Carboxylase Alpha/Bêta
Acyl-CoA Dehydrogenase Short chain/Very Long chain
Acetyl-CoA AcetylTransferase 2
Acetyl-CoA Carboxylase 1 (ACC1 – ACACA)
ATP Citrate LYase
Acyl-CoA Thioesterase 9
Acyl-CoA OXidase 1
Acyl-CoA Synthetase Long chain 1
PKB (Protein Kinase B)
Ankyrin repeat and KH Domain-containing protein 1
Antisense Non-coding RNA in the INK4 Locus
- APO genes:
Adipose Stromal Cells
Adipose triglyceride lipase
B-Cell Lymphoma protein 1/2
Brown fat LNCRNA 1
Cancer Associated Small Integral Membrane ORF 1
Rat hepatocarcinoma cell line
Cluster of Differentiation 36
CDP-Diacylglycerol Synthase 1
CCAAT/Enhancer-Binding Protein Alpha
competing endogenous RNA
Chromatin Isolation by RNA Purification
Human nasopharyngeal carcinoma cell line
Carnitine PalmitoylTransferase 1A
ColoRectal Neoplasia Differentially Expressed
Cytochrome P450 51A1/7A1/8B1
DiGlyceride AcylTransferase 2
DiacylGlycerol Kinase Alpha
Endothelial Differentiation related Factor 1
ELongation Of Very Long chain fatty acids protein 6
Fatty Acid-Binding Protein 4/5
Fatty Acid DeSaturase 2
Fatty Acid Synthase
Farnesyl DiPhosphate Synthase
Fatty Liver Related LncRNA 3/5/8
Farnesoid X Receptor; from NR1H4 gene
Antisense of GENE
Divergent Transcript from GENE
Glycerol-3-Phosphate AcylTransferase 3
G Protein-coupled Receptor 119
Genome-Wide Association Study
Histone 3, Lysine 27
trimethylation of H3K27
HOXD Antisense Growth-associated Long non-coding RNA
- HCT116, HCT 119, HT29:
Human colorectal carcinoma cell line
- HEK-293 T:
Human embryonic kidney cell line
Human cervix adenocarcinoma cell line
Human melanoma cell line
Human hepatocarcinoma cell line
Heterogeneous Nuclear RiboNucleoProtein
HOX Transcript Antisense RNA
Homeobox protein C6
HUman Genome Organisation
Human hepatocarcinoma cell line
Highly Upregulated in Liver Cancer
Human Umbilical Vein Endothelial Cells
Isopentenyl-diphosphate Delta Isomerase 1
Insulin-like Growth Factor 2 Binding Protein 2
INositol Polyphoshate-5-Phosphatase D
Iroquois Homeobox 5
Liver-Expressed LXR-Induced Sequence
lincRNA for ADipogenesis And Lipogenesis
LincRNA for ADipogenesis And Lipogenesis
linRNA-DYNein Light chain RoadBlock-type 2, transcript 2
Long Intergenic Noncoding RNA for Kinase Activation
Long Intergenic noncoding RNA antisense to S1PR1
Liver cell Viability Associated lncRNA
lncRNA Activated in RCC with Sunitinib Resistance
lncRNA HCV Regulated 1
lncRNA-Lysine DeMethylase 5D, transcript 4
lncRNA Liver-Specific Triglyceride Regulator
long noncoding RNA
lncRNA Suppressor of Hepatic Gluconeogenesis and Lipogenesis
lncRNA associated with Lymph Node Metastasis In Cervical Cancer
LysoPhosphatidylCholine AcylTransferase 3
Lysine (K)-Specific Demethylase 1; from KDM1A gene
Liver X Receptor; from NR1H2/3 genes
Metastasis Associated in Lung Adenocarcinoma Transcript 1
Human breast cancer cell line
Maternally Expressed Gene 3
Macrophage-Expressed LXR-Induced Sequence
Human osteosarcoma cell line
Mouse Genome Informatics
MeValonate diphosphate Decarboxylase
Non-Alcoholic Fatty Liver Disease
Nuclear Enriched Abundant Transcript 1
Nuclear Factor I A
NFE2-Related Factor 2; from NFE2L2 gene
Noncoding RNA Repressor Of NFAT
Non-Small Cell Lung Cancer
OLigodendrocyte Maturation-Associated Long Intergenic NonCoding RNA
Open Reading Frame
Polymerase Chain Reaction
Proprotein Convertase Subtilisin/Kexin Type 9
Phosphatidylinositol 4-Kinase Beta
PhosphoLipase A2, Group 1B
PhosphoLipase C Beta 3/Gamma 1
PatatiN-like PhosphoLipase A2
Peroxisome Proliferator-Activated Receptors Alpha/Gamma
Polycomb Repressive Complex 2
Polypyrimidine Tract Binding Protein 1
Plasmacytoma Variant Translocation 1
hnRNP Associated with Lethal Yellow protein
Retinal Non-Coding RNA 3
Reads Per Kilobase of transcript, per Million mapped reads
Reverse Transcription PCR
Sphingosine-1-Phosphate Receptor 1
Antisense of FAS (Fas Cell Surface Death Receptor)
Small Heterodimer Partner
small interfering RNA
Smith-Magenis syndrome Chromosome Region, candidate 2
SMall Integral Membrane protein 22
Small Noncoding Host Gene 16
Single Nucleotide Polymorphism
Steroid Receptor RNA Activator 1
Steroid Receptor RNA Activator Protein
Sterol Regulatory Element Binding transcription Factor 1/2
SUppressor of Zeste 12
Human leukemic monocyte cell line
Triple-Negative Breast Cancer
Tumor Necrosis Factor
TRIBbles homolog 1/3
Human osteosarcoma cell line
ultra Conserved 372
Bergen WG, Mersmann HJ. Comparative aspects of lipid metabolism: impact on contemporary research and use of animal models. J Nutr. 2005;135:2499–502.
Parrish CC. Lipids in marine ecosystems. ISRN Ocenaogr. 2013;2013:1–16.
Li N, Xu C, Li-Beisson Y, Philippar K. Fatty acid and lipid transport in plant cells. Trends Plant Sci. 2016;21:145–58.
Desert C, Baéza E, Aite M, Boutin M, Le Cam A, Montfort J, et al. Multi-tissue transcriptomic study reveals the main role of liver in the chicken adaptive response to a switch in dietary energy source through the transcriptional regulation of lipogenesis. BMC Genomics. 2018;19:187.
Sato K, Kamada T. Regulation of bile acid, cholesterol, and fatty acid synthesis in chicken primary hepatocytes by different concentrations of T0901317, an agonist of liver X receptors. Comp Biochem Physiol A Mol Integr Physiol. 2011;158:201–6.
Hillgartner FB, Salati LM, Goodridge AG. Physiological and molecular mechanisms involved in nutritional regulation of fatty acid synthesis. Physiol Rev. 1995;75:47–76.
Greene DH, Selivonchick DP. Lipid metabolism in fish. Prog Lipid Res. 1987;26:53–85.
Ye J, DeBose-Boyd RA. Regulation of cholesterol and fatty acid synthesis. Cold Spring Harb Perspect Biol. 2011;3:a004754.
Viturro E, Koenning M, Kroemer A, Schlamberger G, Wiedemann S, Kaske M, et al. Cholesterol synthesis in the lactating cow: induced expression of candidate genes. J Steroid Biochem Mol Biol. 2009;115:62–7.
Shreni KD, Jafri AK. Seasonal variations in the total cholesterol content of the liver of cat fish Heteropnuestes fossilis (Bloch). Fish Technol. 1977;14:116–8.
Diéguez C, Vazquez MJ, Romero A, López M, Nogueiras R. Hypothalamic control of lipid metabolism: focus on leptin, ghrelin and melanocortins. Neuroendocrinology. 2011;94:1–11.
Harrow J, Frankish A, Gonzalez JM, Tapanari E, Diekhans M, Kokocinski F, et al. GENCODE: the reference human genome annotation for the ENCODE project. Genome Res. 2012;22:1760–74.
Mudge JM, Harrow J. Creating reference gene annotation for the mouse C57BL6/J genome assembly. Mamm Genome. 2015;26:366–78.
Derrien T, Johnson R, Bussotti G, Tanzer A, Djebali S, Tilgner H, et al. The GENCODE v7 catalog of human long noncoding RNAs: analysis of their gene structure, evolution, and expression. Genome Res. 2012;22:1775–89.
Morris KV, Mattick JS. The rise of regulatory RNA. Nat Rev Genet. 2014;15:423–37.
Mercer TR, Dinger ME, Mattick JS. Long non-coding RNAs: insights into functions. Nat Rev Genet. 2009;10:155–9.
van Solingen C, Scacalossi KR, Moore KJ. Long noncoding RNAs in lipid metabolism. Curr Opin Lipidol. 2018;29:224–32.
Fang S, Zhang L, Guo J, Niu Y, Wu Y, Li H, et al. NONCODEV5: a comprehensive annotation database for long non-coding RNAs. Nucleic Acids Res. 2018;46:D308–14.
Volders P-J, Verheggen K, Menschaert G, Vandepoele K, Martens L, Vandesompele J, et al. An update on LNCipedia: a database for annotated human lncRNA sequences. Nucleic Acids Res. 2015;43(Database issue):D174–80.
Muret K, Klopp C, Wucher V, Esquerré D, Legeai F, Lecerf F, et al. Long noncoding RNA repertoire in chicken liver and adipose tissue. Genet Sel Evol. 2017;49. https://doi.org/10.1186/s12711-016-0275-0.
Gloss BS, Dinger ME. The specificity of long noncoding RNA expression. Biochim Biophys Acta. 2016;1859:16–22.
Kang Y-J, Yang D-C, Kong L, Hou M, Meng Y-Q, Wei L, et al. CPC2: a fast and accurate coding potential calculator based on sequence intrinsic features. Nucleic Acids Res. 2017;45:W12–6.
Kong L, Zhang Y, Ye Z-Q, Liu X-Q, Zhao S-Q, Wei L, et al. CPC: assess the protein-coding potential of transcripts using sequence features and support vector machine. Nucleic Acids Res. 2007;35(Web Server):W345–9.
Wang L, Park HJ, Dasari S, Wang S, Kocher J-P, Li W. CPAT: coding-potential assessment tool using an alignment-free logistic regression model. Nucleic Acids Res. 2013;41:e74.
Lin MF, Jungreis I, Kellis M. PhyloCSF: a comparative genomics method to distinguish protein coding and non-coding regions. Bioinformatics. 2011;27:i275–82.
Wucher V, Legeai F, Hedan B, Rizk G, Lagoutte L, Leeb T, et al. FEELnc: a tool for Long non-coding RNAs annotation and its application to the dog transcriptome. 2016. http://biorxiv.org/lookup/doi/10.1101/064436. Accessed 3 Oct 2016.
Hezroni H, Koppstein D, Schwartz MG, Avrutin A, Bartel DP, Ulitsky I. Principles of long noncoding RNA evolution derived from direct comparison of transcriptomes in 17 species. Cell Rep. 2015;11:1110–22.
Foissac S, Djebali S, Munyard K, Villa-Vialaneix N, Rau A, Muret K, et al. Livestock genome annotation: transcriptome and chromatin structure profiling in cattle, goat, chicken and pig. bioRxiv. 2018. https://doi.org/10.1101/316091.
Ulitsky I. Evolution to the rescue: using comparative genomics to understand long non-coding RNAs. Nat Rev Genet. 2016;17:601–14.
Ulitsky I, Shkumatava A, Jan CH, Sive H, Bartel DP. Conserved function of lincRNAs in vertebrate embryonic development despite rapid sequence evolution. Cell. 2011;147:1537–50.
Chen Z. Progress and prospects of long noncoding RNAs in lipid homeostasis. Mol Metab. 2016;5:164–70.
Wright MW. A short guide to long non-coding RNA gene nomenclature. Hum Genomics. 2014;8:7.
Zhou T, Ding J, Wang X-A, Zheng X. Long noncoding RNAs and atherosclerosis. Atherosclerosis. 2016;248:51–61.
Smekalova EM, Kotelevtsev YV, Leboeuf D, Shcherbinina EY, Fefilova AS, Zatsepin TS, et al. lncRNA in the liver: prospects for fundamental research and therapy by RNA interference. Biochimie. 2016;131:159–72.
Ananthanarayanan M. A novel long noncoding RNA regulating cholesterol and bile acid homeostasis: a new kid on the block and a potential therapeutic target? Hepatology. 2016;64:16–8.
Zhao Y, Wu J, Liangpunsakul S, Wang L. Long non-coding RNA in liver metabolism and disease: current status. Liver Res. 2017;1:163–7.
Sallam T, Jones M, Thomas BJ, Wu X, Gilliland T, Qian K, et al. Transcriptional regulation of macrophage cholesterol efflux and atherogenesis by a long noncoding RNA. Nat Med. 2018;24:304–12.
Zeng Y, Ren K, Zhu X, Zheng Z, Yi G. Long noncoding RNAs: advances in lipid metabolism. Adv Clin Chem. 2018;87:1–36.
Liu G, Zheng X, Xu Y, Lu J, Chen J, Huang X. Long non-coding RNAs expression profile in HepG2 cells reveals the potential role of long non-coding RNAs in the cholesterol metabolism. Chin Med J. 2015;128:91–7.
Lillycrop K, Murray R, Cheong C, Teh AL, Clarke-Harris R, Barton S, et al. ANRIL promoter DNA methylation: a perinatal marker for later adiposity. EBioMedicine. 2017;19:60–72.
Halley P, Kadakkuzha BM, Faghihi MA, Magistri M, Zeier Z, Khorkova O, et al. Regulation of the apolipoprotein gene cluster by a long noncoding RNA. Cell Rep. 2014;6:222–30.
Qin W, Li X, Xie L, Li S, Liu J, Jia L, et al. A long non-coding RNA, APOA4-AS, regulates APOA4 expression depending on HuR in mice. Nucleic Acids Res. 2016;44:6423–33.
Chen Y, Huang H, Xu C, Yu C, Li Y. Long non-coding RNA profiling in a non-alcoholic fatty liver disease rodent model: new insight into pathogenesis. Int J Mol Sci. 2017;18:21.
Zhao X-Y, Li S, DelProposto JL, Liu T, Mi L, Porsche C, et al. The long noncoding RNA Blnc1 orchestrates homeostatic adipose tissue remodeling to preserve metabolic health. Mol Metab. 2018;14:60–70.
Polycarpou-Schwarz M, Groß M, Mestdagh P, Schott J, Grund SE, Hildenbrand C, et al. The cancer-associated microprotein CASIMO1 controls cell proliferation and interacts with squalene epoxidase modulating lipid droplet formation. Oncogene. 2018;37:4750–68.
Ellis BC, Graham LD, Molloy PL. CRNDE, a long non-coding RNA responsive to insulin/IGF signaling, regulates genes involved in central metabolism. Biochim Biophys Acta. 2014;1843:372–86.
Cao C, Fan R, Zhao J, Zhao X, Yang J, Zhang Z, et al. Impact of exudative diathesis induced by selenium deficiency on LncRNAs and their roles in the oxidative reduction process in broiler chick veins. Oncotarget. 2017;8:20695–705.
Reddy MA, Chen Z, Park JT, Wang M, Lanting L, Zhang Q, et al. Regulation of inflammatory phenotype in macrophages by a diabetes-induced long noncoding RNA. Diabetes. 2014;63:4249–61.
Yang L, Li P, Yang W, Ruan X, Kiesewetter K, Zhu J, et al. Integrative transcriptome analyses of metabolic responses in mice define pivotal LncRNA metabolic regulators. Cell Metab. 2016;24:627–39.
Liu C, Yang Z, Wu J, Zhang L, Lee S, Shin D-J, et al. Long noncoding RNA H19 interacts with polypyrimidine tract-binding protein 1 to reprogram hepatic lipid homeostasis. Hepatology. 2018;67:1768–83.
Lu C, Ma J, Cai D. Increased HAGLR expression promotes non-small cell lung cancer proliferation and invasion via enhanced de novo lipogenesis. Tumour Biol. 2017;39:1010428317697574.
Ma D-D, Yuan L-L, Lin L-Q. LncRNA HOTAIR contributes to the tumorigenesis of nasopharyngeal carcinoma via up-regulating FASN. Eur Rev Med Pharmacol Sci. 2017;21:5143–52.
Huang C, Hu Y-W, Zhao J-J, Ma X, Zhang Y, Guo F-X, et al. Long noncoding RNA HOXC-AS1 suppresses ox-LDL-induced cholesterol accumulation through promoting HOXC6 expression in THP-1 macrophages. DNA Cell Biol. 2016;35:722–9.
Cui M, Xiao Z, Wang Y, Zheng M, Song T, Cai X, et al. Long noncoding RNA HULC modulates abnormal lipid metabolism in hepatoma cells through an miR-9-mediated RXRA signaling pathway. Cancer Res. 2015;75:846–57.
Sallam T, Jones MC, Gilliland T, Zhang L, Wu X, Eskin A, et al. Feedback modulation of cholesterol metabolism by the lipid-responsive non-coding RNA LeXis. Nature. 2016;534:124–8.
Zhang X, Wu J, Wu C, Chen W, Lin R, Zhou Y, et al. The LINC01138 interacts with PRMT5 to promote SREBP1-mediated lipid desaturation and cell growth in clear cell renal cell carcinoma. Biochem Biophys Res Commun. 2018;507:337–42.
Zhang X, Xue C, Lin J, Ferguson JF, Weiner A, Liu W, et al. Interrogation of nonconserved human adipose lincRNAs identifies a regulatory role of linc-ADAL in adipocyte metabolism. Sci Transl Med. 2018;10:eaar5987.
Hu Y-W, Yang J-Y, Ma X, Chen Z-P, Hu Y-R, Zhao J-Y, et al. A lincRNA-DYNLRB2-2/GPR119/GLP-1R/ABCA1-dependent signal transduction pathway is essential for the regulation of cholesterol homeostasis. J Lipid Res. 2014;55:681–97.
Lin A, Hu Q, Li C, Xing Z, Ma G, Wang C, et al. The LINK-A lncRNA interacts with PtdIns(3,4,5)P3 to hyperactivate AKT and confer resistance to AKT inhibitors. Nat Cell Biol. 2017;19:238–51.
Josipovic I, Pflüger B, Fork C, Vasconez AE, Oo JA, Hitzel J, et al. Long noncoding RNA LISPR1 is required for S1P signaling and endothelial cell function. J Mol Cell Cardiol. 2018;116:57–68.
Atanasovska B, Rensen SS, van der Sijde MR, Marsman G, Kumar V, Jonkers I, et al. A liver-specific long noncoding RNA with a role in cell viability is elevated in human nonalcoholic steatohepatitis. Hepatology. 2017;66:794–808.
Tristán-Flores FE, Guzmán P, Ortega-Kermedy MS, Cruz-Torres G, de la Rocha C, Silva-Martínez GA, et al. Liver X receptor-binding DNA motif associated with atherosclerosis-specific DNA methylation profiles of Alu elements and neighboring CpG Islands. J Am Heart Assoc. 2018;7:e007686.
Zhang M, Chi X, Qu N, Wang C. Long noncoding RNA lncARSR promotes hepatic lipogenesis via Akt/SREBP-1c pathway and contributes to the pathogenesis of nonalcoholic steatohepatitis. Biochem Biophys Res Commun. 2018;499:66–70.
Huang J, Chen S, Cai D, Bian D, Wang F. Long noncoding RNA lncARSR promotes hepatic cholesterol biosynthesis via modulating Akt/SREBP-2/HMGCR pathway. Life Sci. 2018;203:48–53.
Lan X, Yan J, Ren J, Zhong B, Li J, Li Y, et al. A novel long noncoding RNA Lnc-HC binds hnRNPA2B1 to regulate expressions of Cyp7a1 and Abca1 in hepatocytic cholesterol metabolism. Hepatology. 2016;64:58–72.
Li D, Cheng M, Niu Y, Chi X, Liu X, Fan J, et al. Identification of a novel human long non-coding RNA that regulates hepatic lipid metabolism by inhibiting SREBP-1c. Int J Biol Sci. 2017;13:349–57.
Molina E, Chew GS, Myers SA, Clarence EM, Eales JM, Tomaszewski M, et al. A novel Y-specific long non-coding RNA associated with cellular lipid accumulation in HepG2 cells and atherosclerosis-related genes. Sci Rep. 2017;7:16710.
Lo KA, Huang S, Walet ACE, Zhang Z-C, Leow MK-S, Liu M, et al. Adipocyte long-noncoding RNA transcriptome analysis of obese mice identified Lnc-leptin, which regulates leptin. Diabetes. 2018;67:1045–56.
Li P, Ruan X, Yang L, Kiesewetter K, Zhao Y, Luo H, et al. A liver-enriched long non-coding RNA, lncLSTR, regulates systemic lipid metabolism in mice. Cell Metab. 2015;21:455–67.
Li H, Gu Z, Yang L, Tian Y, Kang X, Liu X. Transcriptome profile analysis reveals an estrogen induced LncRNA associated with lipid metabolism and carcass traits in chickens (Gallus Gallus). Cell Physiol Biochem. 2018;50:1638–58.
Wang J, Yang W, Chen Z, Chen J, Meng Y, Feng B, et al. Long noncoding RNA lncSHGL recruits hnRNPA1 to suppress hepatic gluconeogenesis and lipogenesis. Diabetes. 2018;67:581–93.
Shang C, Wang W, Liao Y, Chen Y, Liu T, Du Q, et al. LNMICC promotes nodal metastasis of cervical Cancer by reprogramming fatty acid metabolism. Cancer Res. 2018;78:877–90.
Lu M-C, Yu H-C, Yu C-L, Huang H-B, Koo M, Tung C-H, et al. Increased expression of long noncoding RNAs LOC100652951 and LOC100506036 in T cells from patients with rheumatoid arthritis facilitates the inflammatory responses. Immunol Res. 2016;64:576–83.
Ghanbari M, Peters MJ, de Vries PS, Boer CG, van Rooij JGJ, Lee Y-C, et al. A systematic analysis highlights multiple long non-coding RNAs associated with cardiometabolic disorders. J Hum Genet. 2018;63:431–46.
Yan C, Chen J, Chen N. Long noncoding RNA MALAT1 promotes hepatic steatosis and insulin resistance by increasing nuclear SREBP-1c protein stability. Sci Rep. 2016;6:22640.
Zhang L, Yang Z, Trottier J, Barbier O, Wang L. Long noncoding RNA MEG3 induces cholestatic liver injury by interaction with PTBP1 to facilitate shp mRNA decay. Hepatology. 2017;65:604–15.
Zhu X, Wu Y-B, Zhou J, Kang D-M. Upregulation of lncRNA MEG3 promotes hepatic insulin resistance via increasing FoxO1 expression. Biochem Biophys Res Commun. 2016;469:319–25.
Wang X, Wang J. High-content hydrogen water-induced downregulation of miR-136 alleviates non-alcoholic fatty liver disease by regulating Nrf2 via targeting MEG3. Biol Chem. 2018;399:397–406.
Huang-Fu N, Cheng J-S, Wang Y, Li Z-W, Wang S-H. Neat1 regulates oxidized low-density lipoprotein-induced inflammation and lipid uptake in macrophages via paraspeckle formation. Mol Med Rep. 2018;17:3092–8.
Liu X, Liang Y, Song R, Yang G, Han J, Lan Y, et al. Long non-coding RNA NEAT1-modulated abnormal lipolysis via ATGL drives hepatocellular carcinoma proliferation. Mol Cancer. 2018;17:90.
Liu Y, Ji Y, Li M, Wang M, Yi X, Yin C, et al. Integrated analysis of long noncoding RNA and mRNA expression profile in children with obesity by microarray analysis. Sci Rep. 2018;8:8750.
Benhammou JN, Ko A, Alvarez M, Kaminska D, Pihlajamäki J, Pisegna JR, et al. Su1496 - The Long Intergenic, Non-Coding RNA, Olmalinc, Influences Lipid Metabolism in Hepatocytes by Regulating SREBP1 and SREBP2, and may Play a Critical Role in the Development of NAFLD. Gastroenterology. 2018;154:S-1158.
Zhou Q, Chen F, Zhao J, Li B, Liang Y, Pan W, et al. Long non-coding RNA PVT1 promotes osteosarcoma development by acting as a molecular sponge to regulate miR-195. Oncotarget. 2016;7:82620–33.
Shan K, Jiang Q, Wang X-Q, Wang Y-N-Z, Yang H, Yao M-D, et al. Role of long non-coding RNA-RNCR3 in atherosclerosis-related vascular dysfunction. Cell Death Dis. 2016;7:e2248.
Mitchel K, Theusch E, Cubitt C, Dosé AC, Stevens K, Naidoo D, et al. RP1-13D10.2 is a novel modulator of statin-induced changes in cholesterol. Circ Cardiovasc Genet. 2016;9:223–30.
Hu Y-W, Zhao J-Y, Li S-F, Huang J-L, Qiu Y-R, Ma X, et al. RP5-833A20.1/miR-382-5p/NFIA-dependent signal transduction pathway contributes to the regulation of cholesterol homeostasis and inflammatory reaction. Arterioscler Thromb Vasc Biol. 2015;35:87–101.
Qi X, Shao M, Sun H, Shen Y, Meng D, Huo W. Long non-coding RNA SNHG14 promotes microglia activation by regulating miR-145-5p/PLA2G4A in cerebral infarction. Neuroscience. 2017;348:98–106.
Christensen LL, True K, Hamilton MP, Nielsen MM, Damas ND, Damgaard CK, et al. SNHG16 is regulated by the Wnt pathway in colorectal cancer and affects genes involved in lipid metabolism. Mol Oncol. 2016;10:1266–82.
Mazar J, Zhao W, Khalil AM, Lee B, Shelley J, Govindarajan SS, et al. The functional characterization of long noncoding RNA SPRY4-IT1 in human melanoma cells. Oncotarget. 2014;5:8959–69.
Chen G, Yu D, Nian X, Liu J, Koenig RJ, Xu B, et al. LncRNA SRA promotes hepatic steatosis through repressing the expression of adipose triglyceride lipase (ATGL). Sci Rep. 2016;6:35531.
Liu S, Sheng L, Miao H, Saunders TL, MacDougald OA, Koenig RJ, et al. SRA gene knockout protects against diet-induced obesity and improves glucose tolerance. J Biol Chem. 2014;289:13000–9.
Douvris A, Soubeyrand S, Naing T, Martinuk A, Nikpay M, Williams A, et al. Functional analysis of the TRIB1 associated locus linked to plasma triglycerides and coronary artery disease. J Am Heart Assoc. 2014;3:e000884.
Guo J, Fang W, Sun L, Lu Y, Dou L, Huang X, et al. Ultraconserved element uc.372 drives hepatic lipid accumulation by suppressing miR-195/miR4668 maturation. Nat Commun. 2018;9:612.
Huang W, Zhang X, Li A, Xie L, Miao X. Differential regulation of mRNAs and lncRNAs related to lipid metabolism in two pig breeds. Oncotarget. 2017;8:87539–53.
Zhao X-Y, Xiong X, Liu T, Mi L, Peng X, Rui C, et al. Long noncoding RNA licensing of obesity-linked hepatic lipogenesis and NAFLD pathogenesis. Nat Commun. 2018;9:2986.
Ruan X, Li P, Cangelosi A, Yang L, Cao H. A long non-coding RNA, lncLGR, regulates hepatic Glucokinase expression and glycogen storage during fasting. Cell Rep. 2016;14:1867–75.
Willingham AT, Orth AP, Batalov S, Peters EC, Wen BG, Aza-Blanc P, et al. A strategy for probing the function of noncoding RNAs finds a repressor of NFAT. Science. 2005;309:1570–3.
Bierhoff H. Analysis of lncRNA-protein interactions by RNA-protein pull-down assays and RNA immunoprecipitation (RIP). Methods Mol Biol. 2018;1686:241–50.
Boivin V, Deschamps-Francoeur G, Scott MS. Protein coding genes as hosts for noncoding RNA expression. Semin Cell Dev Biol. 2018;75:3–12.
Shenker S, Miura P, Sanfilippo P, Lai EC. IsoSCM: improved and alternative 3′ UTR annotation using multiple change-point inference. RNA. 2015;21:14–27.
Fan R, Cao C, Zhao X, Shi Q, Zhao J, Xu S. Downregulated long noncoding RNA ALDBGALG0000005049 induces inflammation in chicken muscle suffered from selenium deficiency by regulating stearoyl-CoA desaturase. Oncotarget. 2017;8:52761–74.
Szafron LM, Balcerak A, Grzybowska EA, Pienkowska-Grela B, Felisiak-Golabek A, Podgorska A, et al. The novel gene CRNDE encodes a nuclear peptide (CRNDEP) which is overexpressed in highly proliferating tissues. PLoS One. 2015;10:e0127475.
Lanz RB, McKenna NJ, Onate SA, Albrecht U, Wong J, Tsai SY, et al. A steroid receptor coactivator, SRA, functions as an RNA and is present in an SRC-1 complex. Cell. 1999;97:17–27.
Liu C, Wu H-T, Zhu N, Shi Y-N, Liu Z, Ao B-X, et al. Steroid receptor RNA activator: biologic function and role in disease. Clin Chim Acta. 2016;459:137–46.
Kawashima H, Takano H, Sugita S, Takahara Y, Sugimura K, Nakatani T. A novel steroid receptor co-activator protein (SRAP) as an alternative form of steroid receptor RNA-activator gene: expression in prostate cancer cells and enhancement of androgen receptor activity. Biochem J. 2003;369(Pt 1):163–71.
Cooper C, Vincett D, Yan Y, Hamedani MK, Myal Y, Leygue E. Steroid receptor RNA activator bi-faceted genetic system: heads or tails? Biochimie. 2011;93:1973–80.
Kumar S, Hedges SB. A molecular timescale for vertebrate evolution. Nature. 1998;392:917–20.
Hedges SB, Kumar S. Genomics. Vertebrate genomes compared. Science. 2002;297:1283–5.
Kerner P, Ikmi A, Coen D, Vervoort M. Evolutionary history of the Iroquois/Irx genes in metazoans. BMC Evol Biol. 2009;9:74.
Fagerberg L, Hallström BM, Oksvold P, Kampf C, Djureinovic D, Odeberg J, et al. Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics. Mol Cell Proteomics. 2014;13:397–406.
Schmitz SU, Grote P, Herrmann BG. Mechanisms of long noncoding RNA function in development and disease. Cell Mol Life Sci. 2016;73:2491–509.
Perry RB-T, Ulitsky I. The functions of long noncoding RNAs in development and stem cells. Development. 2016;143:3882–94.
Ponting CP, Oliver PL, Reik W. Evolution and functions of long noncoding RNAs. Cell. 2009;136:629–41.
Breschi A, Gingeras TR, Guigó R. Comparative transcriptomics in human and mouse. Nat Rev Genet. 2017;18:425–40.
Le Béguec C, Wucher V, Lagoutte L, Cadieu E, Botherel N, Hédan B, et al. Characterisation and functional predictions of canine long non-coding RNAs. Sci Rep. 2018;8:13444.
Hocquette JF, Gondret F, Baéza E, Médale F, Jurie C, Pethick DW. Intramuscular fat content in meat-producing animals: development, genetic and nutritional control, and identification of putative markers. Animal. 2010;4:303–19.
Wood JD, Enser M, Fisher AV, Nute GR, Sheard PR, Richardson RI, et al. Fat deposition, fatty acid composition and meat quality: a review. Meat Sci. 2008;78:343–58.
Listrat A, Lebret B, Louveau I, Astruc T, Bonnet M, Lefaucheur L, et al. How muscle structure and composition influence meat and flesh quality. ScientificWorldJournal. 2016;2016:3182746.
Li A, Zhang J, Zhou Z, Wang L, Liu Y, Liu Y. ALDB: a domestic-animal long noncoding RNA database. PLoS One. 2015;10:e0124003.
Letunic I, Bork P. Interactive tree of life (iTOL) v3: an online tool for the display and annotation of phylogenetic and other trees. Nucleic Acids Res. 2016;44:W242–5.
We thank Christine Kervarrec from the UMR 1085 IRSET-INSERM (Rennes, France) for murine genomic DNA.
KM is a Ph.D. fellow supported by the Brittany region (France) and the INRA’s Animal Genetics division. The animal experimental designs and RNA-Seq data were funded by the French National Agency of Research (FatInteger Project, ANR-11-SVS7 and ChickStress Project, ANR-13-ADAP).
Ethics approval and consent to participate
All experiments were conducted following the French National Guidelines for the care and use of animals in research edited by the French Ministries of Higher Education and Scientific Research, and of Agriculture and Fisheries (http://ethique.ipbs.fr/charteexpeanimale.pdf). The protocol was also approved by the local Ethics Committee of Val de Loire, France (authorization to experiment on living animals n°7740, 30/03/2012). The human tissue samples from which RNAseq data were collected and used in this study were approved by the Uppsala Ethical Review Board (Reference #2011/473) according to Fagerberg et al. .
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The authors declare that they have no competing interests.
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Gene structure of HMGCR. In blue: HMGCR isoforms from Ensembl. In green: lncRNA AT102202 with 3 exons in common with HMGCR isoforms. In purple: position of the siRNA used by Liu et al. for the AT10202 knockdown and in red, primers used for the expression evaluation. Empty blocks represent noncoding regions. HMGCR isoforms that encode the HMGCR protein are the first 3 models.
List of primers used for model validation by RT-PCR.
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Muret, K., Désert, C., Lagoutte, L. et al. Long noncoding RNAs in lipid metabolism: literature review and conservation analysis across species. BMC Genomics 20, 882 (2019). https://doi.org/10.1186/s12864-019-6093-3
- Lipid metabolism