- Research article
- Open Access
Genome-wide analysis of the NAC transcription factor family in broomcorn millet (Panicum miliaceum L.) and expression analysis under drought stress
BMC Genomics volume 21, Article number: 96 (2020)
Broomcorn millet is a drought-tolerant cereal that is widely cultivated in the semiarid regions of Asia, Europe, and other continents; however, the mechanisms underlying its drought-tolerance are poorly understood. The NAM, ATAF1/2, and CUC2 (NAC) transcription factors form a large plant-specific gene family that is involved in the regulation of tissue development and abiotic stress. To date, NAC transcription factors have not been systematically researched in broomcorn millet.
In the present study, a total of 180 NAC (PmNAC) genes were identified from the broomcorn millet genome and named uniformly according to their chromosomal distribution. Phylogenetic analysis demonstrated that the PmNACs clustered into 12 subgroups, including the broomcorn millet-specific subgroup Pm_NAC. Gene structure and protein motif analyses indicated that closely clustered PmNAC genes were relatively conserved within each subgroup, while genome mapping analysis revealed that the PmNAC genes were unevenly distributed on broomcorn millet chromosomes. Transcriptome analysis revealed that the PmNAC genes differed greatly in expression in various tissues and under different drought stress durations. The expression of 10 selected genes under drought stress was analyzed using quantitative real-time PCR.
In this study, 180 NAC genes were identified in broomcorn millet, and their phylogenetic relationships, gene structures, protein motifs, chromosomal distribution, duplication, expression patterns in different tissues, and responses to drought stress were studied. These results will be useful for the further study of the functional characteristics of PmNAC genes, particularly with regards to drought resistance.
Transcription factors (TFs) play an important role in controlling a variety of vital growth and development processes, such as signal transduction, cellular morphogenesis, and response to environmental stressors, during the growth and development of plants [1, 2]. The NAC family is one of the largest groups of plant-specific TFs . The term NAC derives from three proteins: no apical meristem (NAM), Arabidopsis transcription activation factor (ATAF)1/2, and cup-shaped cotyledon (CUC2). Typical NAC proteins exhibit a highly conversed N-terminal DNA-binding domain containing ~ 150 amino acids, which is divided into five subdomains (A–E) .
NAC TFs play important regulatory roles in various aspects of plant growth, development, and adaptation to the environment, including in shoot apical meristem formation , cell division and expansion [6, 7] nutrient remobilization , flower formation , lateral root development [10, 11], leaf senescence [12,13,14,15,16], secondary cell wall biosynthesis [3, 17,18,19,20], fiber development [19, 21, 22], fruit ripening [23, 24], seed development , response to pathogen infection [26,27,28,29,30], and abiotic stress tolerance [31,32,33]. Many studies have confirmed that many NAC genes play crucial roles in the regulation of plant tolerance to drought. Overexpression of CarNAC4, a chickpea TF, enhanced drought tolerance in Arabidopsis thaliana . TaNAC29, a NAC TF from wheat, enhanced salt and drought tolerance in transgenic A. thaliana . Overexpression of the Miscanthus lutarioriparius NAC gene MlNAC5 conferred enhanced drought and cold tolerance in A. thaliana . NAC genes have also been found to increase tolerance to drought stress in rice. For instance, drought resistance in rice was enhanced by the overexpression of SNAC1 , ONAC022 , and ONAC045 . OsNAC10-overexpressing rice plants showed an increased grain yield under both normal and drought conditions . Therefore, NAC family genes are crucial regulators of plant tolerance to drought.
Broomcorn millet (Panicum miliaceum L.), also called proso millet, common millet, and hog millet, is a short-season, drought-tolerant, and barren-tolerant cereal that is widely cultivated in the semiarid regions of Asia, Europe, and other continents. The grains of broomcorn millet not only have high nutritional value, containing abundant proteins, starch, and a variety of vitamins and minerals, but also have medicinal value and are used in millet wine and other products. The NAC gene family has been widely studied in many species, such as A. thaliana , rice , wheat [42, 43], tartary buckwheat , maize [45, 46], foxtail millet , soybean , potato , Chinese cabbage , pepper , cassava , melon , physic nut , apple , and pigeon pea . However, no systematic study of the NAC family in broomcorn millet is available. The genome of broomcorn millet was recently published, providing an important resource for further molecular research in this species . In addition, large RNA sequencing (RNA-seq) expression data from different tissues are also available . Based on these data, NAC gene family members in broomcorn millet were identified in the present study. A phylogenetic tree was constructed, gene exon/intron and conversed motif structural analyses were performed, chromosomal location and synteny analysis were carried out, and the tissue-specific expression patterns of NAC genes in broomcorn millet were surveyed. In addition, the differential expression of NAC genes was analyzed in broomcorn millet under drought conditions using transcriptomics and quantitative real-time PCR (qRT-PCR). This research is the first to detail the NAC gene family in broomcorn millet, which may help elucidate the molecular mechanisms underlying drought stress responses in this important food crop.
Identification and phylogenetic analysis of the PmNAC genes in broomcorn millet
A total of 180 PmNAC genes were identified and were named PmNAC001 to PmNAC180 according to their chromosome location. These were confirmed and used for further analyses (Additional file 1: Table S1). All the PmNAC proteins contained a conserved NAC domain (PF01849) or NAM domain (PF02365).
Phylogenetic analysis of the NAC proteins from broomcorn millet and Arabidopsis was conducted to explore the evolutionary relationships among broomcorn millet NAC proteins. The results demonstrated that the PmNAC proteins could be divided into 12 subgroups according to clade and the classification from Arabidopsis, including a broomcorn millet-specific subgroup named Pm_NAC (Fig. 1, 2a). In our analysis, no NAC members from the subgroups ANAC001, SEUN5, ANAC3, and ANAC011 were identified. Subgroup ANAC063 contained the most PmNAC proteins, namely 52, while subgroup TIP contained only two PmNAC proteins.
Protein properties and sequence analyses
The protein properties were analysed, and the results are summarized in Additional file 1: Table S2. The length and molecular mass of the PmNAC proteins varied greatly, with lengths ranging from 67 to 1435 amino acids (aa) and molecular weights (MWs) ranging from 7.53 to 162.48 kDa. The theoretical isoelectric point (pI) varied greatly from 4.13 to 11.38. Most PmNAC proteins (149 out of 180) were considered unstable due to the instability index being higher than 40. The PmNAC proteins contained a predicted aliphatic index ranging from 45.59 to 101.24. All PmNAC proteins were predicted to be hydrophilic due to the relatively low average hydropathy (GRAVY) value (< 0), with the exception of PmNAC005 and PmNAC165.
Gene structural diversity is an important component of gene family evolution and further supports phylogenetic groupings . Gene structure analysis indicated that the number of introns of PmNAC genes varied from 0 to 14 (Fig. 2b), with 44 PmNAC genes lacking introns. Most PmNAC genes (134 out of 180) contained one to six introns. PmNAC41 had the highest number of introns (14), followed by PmNAC148 with 13 introns. Generally, closely clustered PmNAC genes in the phylogenetic tree exhibited similar exon-intron structures. Most PmNAC genes had no introns in subgroup ANAC063, and there was an average of four introns in subgroup ONAC003.
To further investigate the structural features of broomcorn millet NACs, the conserved motif distributions were analysed. A total of 20 conserved motifs (referred to as motifs 1–20) were identified by MEME, with more motifs located within the N-terminal region than within the C-terminal region (Fig. 2c). The features of these protein motifs are listed in Additional file 1: Table S3. In this analysis, most of the closely related members in the phylogenetic tree showed common motifs in terms of alignment and position, which suggested that the NAC members that clustered along the same branch may possess similar biological functions.
Chromosomal location and synteny analysis of PmNAC genes
All the PmNAC genes were unevenly distributed on broomcorn millet chromosomes, except PmNAC178–180 (Fig. 3). Chromosome 5 (Chr5) contained the highest number of PmNAC genes (n = 17), followed by Chr8 (n = 15) and then Chr3, which had 14 members. In addition, 13, 12, and 11 PmNAC genes were detected on Chr4, Chr6, and Chr12, respectively. Ten PmNAC genes were found on each of Chr1, Chr10, and Chr17. Nine genes were located on Chr11 and seven NAC genes were located on Chr15. Eight PmNAC genes were distributed on each of Chr2, Chr7, Chr13, and Chr14, and six PmNAC genes were found on both Chr16 and Chr18. There were only five PmNAC genes on Chr9.
To identify the duplication events in PmNAC genes, a collinearity analysis was performed using MCScanX software. There were 84 pairs of segmentally duplicated PmNAC genes (Fig. 4) and five groups of tandem duplicated PmNAC genes (Figs. 3, 4; PmNAC029/030/031, PmNAC053/054/055, PmNAC087/088, PmNAC136/137, PmNAC168/169). Duplicated genes were the most common on Chr3, followed by Chr5 and Chr10 (Fig. 4).
Expression pattern analysis of PmNAC genes in different tissues
To better understand the function of PmNAC genes in broomcorn millet, the transcription levels of PmNAC genes in different tissues, i.e., seedlings at one week of age, shoots at three weeks of age, leaf blades, leaf sheaths, stems, inflorescences, and roots at the eight weeks of age, and mature seeds at 12 weeks of age, were investigated using publicly available transcriptome datasets . The Fragments Per Kilobase per Million mapped reads (FPKM) values of the PmNAC genes are listed in Additional file 1: Table S4, and a hierarchical clustering analysis and heatmap were generated to display the expression patterns of the PmNAC genes (Fig. 5).
The expression of three PmNAC genes (PmNAC055, 178, and 179) was not detected in any analysed tissue, possibly due to variations in spatial and temporal expression patterns. The expression of 15 PmNAC genes (PmNAC005, 010, 038, 051, 071, 073, 087, 092, 104, 118, 124, 144, 166, 171, and 180) was detected only in one tissue. Thirteen PmNAC genes (PmNAC001, 004, 009, 026, 028, 037, 039, 045, 063, 101, 108, 132, and 175) exhibited high expression (FPKM > 20) in all the tested tissues, suggesting key roles of these genes in tissue development. In addition, of all the analyzed tissues, there were 10, 16, 10, 12, 18, 29, 55, and 27 PmNAC genes exhibiting the highest expression in seedlings at one week of age, shoots at three weeks of age, and the leaf blades, leaf sheaths, stems, inflorescences, and roots at eight weeks of age, and mature seed at 12 weeks of age, respectively, demonstrating that different PmNAC genes may play different roles in the growth and tissue development of broomcorn millet. The high expression of many PmNAC genes (31%) in the roots may be one explanation for the observed rapid response of broomcorn millet to drought stress. Understanding the expression patterns of PmNAC genes in different tissues can provide a foundation for identifying functional genes in broomcorn millet.
Responses of PmNAC genes to drought treatments
To detect the dynamic changes in the transcription levels of broomcorn millet NAC genes under drought stress, transcriptomic analysis was conducted at 0 h (CK), 1 h (T1), 3 h (T2), and 6 h (T3) under drought treatment (Additional file 1: Table S5). There were 117 PmNAC genes detected in the experiment. A heatmap representing the expressions of the detected PmNAC genes was constructed (Fig. 6a), and trend analysis was carried out to explore the time-related dynamic changes under drought stress (Fig. 6b). The expression of 27 PmNAC genes (PmNAC003, 014, 019, 026, 028, 030, 033, 037, 048, 068, 081, 083, 084, 091, 095, 098, 101, 108, 113, 116, 128, 132, 160, 162, 163, 172, and 175) increased as the time under drought stress progressed in profile1. The expression of 22 PmNAC genes (PmNAC001, 008, 025, 039, 041, 054, 059, 063, 067, 075, 082, 085, 088, 089, 102, 110, 120, 142, 150, 154, 156, and 161) showed an ‘N’ shape and peaked at 6 h in profile2, while the expression of 10 PmNAC genes (PmNAC006, 013, 040, 050, 106, 109, 112, 147, 174, and 177) demonstrated an opposite trend in profile5. The expressions of 11 (PmNAC004, 007, 009, 023, 045, 060, 093, 107, 141, 152, and 170) and seven (PmNAC018, 043, 044, 061, 072, 135, and 148) PmNAC genes showed similar ‘V’ shape trends in profiles 3 and 6, respectively. The expressions of 10 (PmNAC011, 027, 032, 042, 057, 062, 064, 097, 105, and 131) and seven (PmNAC012, 052, 058, 158, 165, 167, and 176) PmNAC genes first increased but then decreased in profiles 4 and 7, respectively.
To verify the RNA-Seq data, 10 PmNAC genes (PmNAC001, 007, 023, 041, 091, 093, 154, 155, 172, and 176) from different subgroups were randomly selected and tested by qRT-PCR. Most of the tested PmNAC genes were up-regulated under drought stress (Fig. 7). Four PmNAC genes (PmNAC041, 091, 093, and 172) increased with time under drought stress, showing similar trends with the RNA-Seq data. The trend of an initial increase and then decrease in PmNAC176 was consistent with the RNA-Seq data. The expression level of PmNAC001 was up-regulated under drought stress compared with the control in both the qRT-PCR results and RNA-Seq data. The expression level of PmNAC154 also increased under drought stress compared with the control in both methods, except for T2 in the RNA-Seq analysis.
NAC TFs play an important role in regulating plant growth and tolerance against various abiotic and biotic stresses. Most of the NAC TFs studied to date are involved in the regulation of developmental progress and the response to abiotic stress. However, few NAC TFs involved in the drought stress response have been identified in broomcorn millet. Therefore, the goal of this study was to obtain further insight into the expression patterns and putative functions of PmNAC genes. In the present study, we investigated the features of PmNAC genes at the genome level. Their tissue expression patterns and responses to drought stress were analyzed. Based on gene expression analyses, we identified significant drought-responsive genes. The present study has furthered our understanding of PmNAC genes and has provided insight into the functions of PmNAC genes.
A total of 180 NAC genes were identified in broomcorn millet. The number of NAC genes in broomcorn millet was higher than the 117 in A. thaliana , 151 in rice , 104 in pepper , 82 in melon , 96 in cassava , 152 in maize , 147 in foxtail millet , 152 in soybean , and 110 in potato , and lower than that of 288 in bread wheat  and 188 in Chinese cabbage . There were extensive variations in gene length, predicted protein MW, and protein pI, whereas the gene structures and protein motifs were relatively conserved in the clades, which provided a valuable reference for their analysis and function. This result confirms that genes originating from the progenitors can evolve gradually and expand. It is well known that gene duplication events are important in the rapid expansion and evolution of gene families. A collinearity analysis of the PmNAC genes in this study showed that there were 84 pairs of segmental duplications and five groups of tandem duplications. Tandem gene duplication of NAC genes has been observed in many species, including A. thaliana, rice, potato, and others.
All 180 PmNAC members were divided into 12 subgroups based on their sequence homology and classification from Arabidopsis . Phylogenetic analysis divided tartary buckwheat, cassava and pepper NACs into 15, 16 and 14 subgroups, respectively [44, 45, 51]. These data indicated that NAC proteins showed diversity in different species. The analysis regarding the conserved motifs of the broomcorn millet proteins further corroborates the categorization of the PmNAC family. The motifs of transcription factors are often related to protein interaction, transcriptional activity and DNA binding . The conserved motifs in the N-terminus of the NAC genes have highly conserved DNA-binding abilities (Fig. 2 c), which indicates that these motifs are very important for the function of NAC genes. Although conserved motifs were similar among many PmNAC proteins, a number of differences in chemical-physical characteristics were also detected for PmNAC members. These differences may due to the amino acid discrepancies in the non-conserved regions of PmNAC members, implying that different PmNAC proteins may act different functions in their own microenvironments.
The tissue-specific expression patterns of PmNAC genes might enable the combinatorial usage of PmNAC genes in the transcriptional regulation of different tissues, whereas ubiquitously expressed PmNAC genes might regulate the transcription of a broad set of genes. For example, PmNAC092, PmNAC051, and PmNAC005 were only detected in the mature seeds and thus may be useful in regulating processes in mature seeds. This phenomenon was also observed in other plants, such as in tartary buckwheat and cassava [44, 52]. Moreover, several reports have indicated that overexpression of tissue-specifically expressed NAC genes can promote the development of particular tissues, as NAC4 from tomato promoted fruit ripening and carotenoid accumulation , cotton NAC transcription factor 1 was involved in secondary cell wall biosynthesis and modification of fibers . Seven highly expressed PmNAC genes (FPKM > 20 in all the tested tissues) originated from subgroup Pm_NAC, suggesting the important roles of the broomcorn millet-specific subgroup Pm_NAC in plant growth and development. Thus, the PmNAC genes with tissue-specific expression were speculated to have important regulatory functions in the associated tissues, providing insight into their utilization in improving the growth and development of various tissues.
Gene expression pattern analysis can facilitate the determination of gene function. In order to identify the expression profiles of broomcorn millet NAC genes in response to drought stress, we performed transcriptomic analysis of the PmNAC genes in broomcorn millet plants subjected to 0 h, 1 h, 3 h, and 6 h of drought. Drought treatment increased the expression of 27 PmNAC genes originating from nine subgroups, of which the subgroup NAC2 contained the largest number (seven). The seven PmNAC genes were closed linked to ANAC082, 103, 013, 016, and 017 in Arabidopsis, which are involved in the abiotic stress response [61, 62] and mitochondrial retrograde signaling [63, 64]. Notably, some PmNAC genes exhibited differential responses to drought at transcriptional levels, although they showed close phylogenetic relationships. Ten PmNAC genes were studied under drought stress using qRT-PCR, and most of the PmNAC genes showed similar trends with the RNA-Seq data. In combination, the transcriptional response of PmNAC genes to drought stress provides a foundation for further investigations into the mechanisms underlying the strong drought tolerance in broomcorn millet.
To conclude, 180 NAC genes were identified in broomcorn millet in the current study. We investigated the features of the PmNAC genes at the genome level, and the tissue expression patterns and responses to drought stress were analysed. Genome-wide expression analysis of NAC genes in response to drought provides an opportunity to further understand the mechanisms involved in the strong drought-tolerance of broomcorn millet.
Identification and phylogenetic analysis of NAC genes in broomcorn millet
The genome of broomcorn millet (accession number GWHAAEZ00000000) was downloaded from the Genome Warehouse in the BIG Data Center (http://bigd.big.ac.cn/gwh). The NAC family databases of Arabidopsis and rice were downloaded from The Arabidopsis Information Resource (TAIR9) (www.arabidopsis.org) and the Rice Genome Annotation Project (http://rice.plantbiology.msu.edu/). The PmNAC genes were obtained using two methods. First, the Hidden Markov Model (HMM) files of the NAC (PF01849) and NAM (PF02365) domains were downloaded from Pfam (http://pfam.xfam.org/) for the identification of NAC proteins (E-value < 0.001). Second, all ANAC and OsNAC proteins were used as queries to search against the broomcorn millet database using default parameters. All the possible PmNACs were confirmed using the Conserved Domains Database (CDD) (http://www.ncbi.nlm.nih.gov/cdd/) and PFAM databases (https://pfam.xfam.org). Only the sequences with full-length NAC or NAM domains were considered as PmNAC proteins and used for further analyses.
MEGA-X (https://www.megasoftware.net/) was used for the evolutionary and phylogenetic analyses. A total of 180 PmNACs and 105 AtNACs were used to generate an unrooted phylogenetic tree using the neighbour-joining method with 1000 bootstrap replications and pairwise detection. According to the classification of AtNACs, all the identified PmNACs were divided into different groups. The gene IDs of the A. thaliana NAC members were listed in Additional file 1: Table S6.
Protein properties and sequence analyses
ProtParam (http://web.expasy.org/protparam/) was used for the prediction of the physical and chemical features of the PmNAC proteins. To ensure the subcellular localization of the identified PmNAC proteins, WoLF PSORT was used to predict the protein sequences (https://wolfpsort.hgc.jp/). TMHMM Server v2.0 (http://www.cbs.dtu.dk/services/TMHMM/) was used for the transmembrane helices in the proteins.
To identify the conserved motifs, the MEME tool (http://meme-suite.org/tools/meme) was used with default parameters, except for the maximum number of motifs, which was set to 15. The gene structure of the broomcorn millet NACs was determined using the Gene Structure Display Server (GSDS) 2.0 (http://gsds.cbi.pku.edu.cn/) program.
Chromosomal mapping and gene duplication analysis
Every NAC gene was matched with the chromosomes of broomcorn millet based on the genome annotations of broomcorn millet. MapGene2Chrome (http://mg2c.iask.in/mg2c_v2.0/) was used to draft the map. MCScanX (default parameters) was used to examine duplicated genes .
Expression patterns of PmNAC genes in different tissues
The transcriptome data available online were used to explore the expression patterns of PmNAC genes in various tissues and different growth stages of broomcorn millet . Seedlings at one week of age, shoots at three weeks of age, leaf blades, leaf sheaths, stems, inflorescences, and roots at eight weeks of age, and mature seeds at 12 weeks of age were sampled to investigate the expression patterns of PmNAC genes. Subsequently, FPKM values were calculated to evaluate the gene expression values and the heatmap (Fig. 5) was generated using pheatmap.
Broomcorn millet plant preparation and drought treatments
The broomcorn millet cultivar Yanshu5 was chosen as the experimental material due to its strong ability to adapt to drought and its relatively high yield . The seeds were planted in flowerpots and grown in a light incubator under the conditions of a 25 °C 14 h photoperiod, and a 22 °C 10 h dark period. They were subjected to drought stress treatments using 20% polyethylene glycol (PEG) 6000 for 0, 1, 3, and 6 h at the 7-d-old stage. The broomcorn millet seedlings were then collected and immediately frozen in liquid nitrogen until RNA extraction.
Transcriptome and qRT-PCR analysis
The total RNA of the whole seedlings was extracted with TRIzol (Invitrogen) and resequenced using an Illumina HiSeq 4000 (Majorbio) in accordance with the standard Illumina protocol. RNA was used for the reverse transcription of cDNA using HiScript II Q RT SuperMix for qPCR (+gDNA wiper) (Vazyme, China). Primer 5.0 was used to design the primers (Additional file 1: Table S7). The PCR reaction system contained 0.2 μL of forward primer, 0.2 μL of reverse primer, 1 μL of cDNA, 5 μL of 2 × ChamQ SYBR qPCR Master Mix (Vazyme, China), and 3.6 μL of nuclease-free H2O. The protocol was as follows: 95 °C for 30 s, followed by 45 cycles of 95 °C for 10 s, and 60 °C for 30 s. Each reaction was performed three times, and the 2-ΔΔCT method  was used to calculate the relative gene expression levels.
Availability of data and materials
All data generated or analyzed during this study are included in this article and its additional files.
Fragments Per Kilobase of transcript per Million mapped reads
He Z, Jinpu J, Liang T, Yi Z, Xiaocheng G, Ge G, Jingchu L. PlantTFDB 2.0: update and improvement of the comprehensive plant transcription factor database. Nucleic Acids Res. 2011;39(Database issue):D1114.
Riaño-Pachón DM, Ruzicic S, Dreyer I, Mueller-Roeber B. PlnTFDB: an integrative plant transcription factor database. BMC Bioinformatics. 2007;8(1):42.
Yao D. Comparative genomic analysis of NAC transcriptional factors to dissect the regulatory mechanisms for cell wall biosynthesis. BMC Bioinformatics. 2012;13(Suppl 15):S10.
Ooka H, Satoh K, Doi K, Nagata T, Otomo Y, Murakami K, Matsubara K, Osato N, Kawai J, Carninci P, et al. Comprehensive analysis of NAC family genes in Oryza sativa and Arabidopsis thaliana. DNA Res. 2003;10(6):239.
Youn-Sung K, Sang-Gyu K, Jung-Eun P, Hye-Young P, Mi-Hye L, Nam-Hai C, Chung-Mo P. A membrane-bound NAC transcription factor regulates cell division in Arabidopsis. Plant Cell. 2006;18(11):3132–44.
Souer E, Houwelingen AV, Kloos D, Mol J, Koes R. The no apical meristem gene of Petunia is required for pattern formation in embryos and flowers and is expressed at meristem and primordia boundaries. Cell. 1996;85(2):159–70.
Takada S, Hibara K, Ishida T, Tasaka M. The CUP-SHAPED COTYLEDON1 gene of Arabidopsis regulates shoot apical meristem formation. Dev. 2001;128(7):1127.
Cristobal U, Assaf D, Tzion F, Ann B, Jorge D. A NAC gene regulating senescence improves grain protein, zinc, and iron content in wheat. Sci. 2006;314(5803):1298–301.
Sablowski RWM, Meyerowitz EM. A homolog of NO APICAL MERISTEM is an immediate target of the floral homeotic genes APETALA3/PISTILLATA. Cell. 1998;92(1):93–103.
Xie Q, Frugis G, Colgan D, Chua NH. Arabidopsis NAC1 transduces auxin signal downstream of TIR1 to promote lateral root development. Genes Dev. 2000;14(23):3024–36.
He X, Mu R, Cao W, Zhang Z, Zhang J, Chen S. AtNAC2, a transcription factor downstream of ethylene and auxin signaling pathways, is involved in salt stress response and lateral root development. Plant J. 2010;44(6):903–16.
Mao C, Lu S, Lv B, Zhang B, Shen J, He J, Luo L, Xi D, Chen X, Ming F. A rice NAC transcription factor promotes leaf senescence via ABA biosynthesis. Plant Physiol. 2017;174(3):1747–63.
Guo Y, Gan S. AtNAP, a NAC family transcription factor, has an important role in leaf senescence. Plant J. 2010;46(4):601–12.
Yang SD, Seo PJ, Yoon HK, Park CM. The Arabidopsis NAC transcription factor VNI2 integrates abscisic acid signals into leaf senescence via the COR/RD genes. Plant Signal Behav. 2011;23(6):2155–68.
Ma X, Zhang Y, Turečková V, Xue GP, Fernie AR, Muellerroeber B, Balazadeh S. The NAC transcription factor SlNAP2 regulates leaf senescence and fruit yield in tomato. Plant Physiol. 2018;177(3):292–2018.
Ye-Sol K, Yasuhito S, Su-Hyun H, Soo-Cheul Y, Nam-Chon P. Mutation of the Arabidopsis NAC016 transcription factor delays leaf senescence. Plant Cell Physiol. 2013;54(10):1660–72.
Ye Y, Wu K, Chen J, Liu Q, Wu Y, Liu B, Fu X. OsSND2, a NAC family transcription factor, is involved in secondary cell wall biosynthesis through regulating MYBs expression in rice. Rice. 2018;11(1):36.
Zhong R, Demura T, Ye ZH. SND1, a NAC domain transcription factor, is a key regulator of secondary wall synthesis in fibers of Arabidopsis. Plant Cell. 2006;18(11):3158–70.
Zhang J, Huang GQ, Zou D, Yan JQ, Li Y, Hu S, Li XB. The cotton (Gossypium hirsutum) NAC transcription factor (FSN1) as a positive regulator participates in controlling secondary cell wall biosynthesis and modification of fibers. New Phytol. 2017;217(2):625–40.
Zhong R, Richardson EA, Ye ZH. Two NAC domain transcription factors, SND1 and NST1, function redundantly in regulation of secondary wall synthesis in fibers of Arabidopsis. Planta. 2007;225(6):1603–11.
Ko J, Yang S, Park AO, Han K. ANAC012, a member of the plant-specific NAC transcription factor family, negatively regulates xylary fiber development in Arabidopsis thaliana. Plant J. 2010;50(6):1035–48.
Sun H, Hu M, Li J, Chen L, Li M, Zhang S, Zhang X, Yang X. Comprehensive analysis of NAC transcription factors uncovers their roles during fiber development and stress response in cotton. BMC Plant Biol. 2018;18(1):150.
Zhu M, Chen G, Zhou S, Tu Y, Wang Y, Dong T, Hu Z. A new tomato NAC (NAM/ATAF1/2/CUC2) transcription factor, SlNAC4, functions as a positive regulator of fruit ripening and carotenoid accumulation. Plant Cell Physiol. 2014;55(1):119–35.
Kou X, Liu C, Han L, Wang S, Xue Z. NAC transcription factors play an important role in ethylene biosynthesis, reception and signaling of tomato fruit ripening. Mol Gen Genomics. 2016;291(3):1205–17.
Han QQ, Song YZ, Zhang JY, Liu LF. Studies on the role of the SlNAC3 gene in regulating seed development in tomato (Solanum lycopersicum). J Hortic Sci Biotechnol. 2014;89(4):423–9.
Oh SK, Lee S, Yu SH, Choi D. Expression of a novel NAC domain-containing transcription factor (CaNAC1) is preferentially associated with incompatible interactions between chili pepper and pathogens. Planta. 2005;222(5):876–87.
Ren T, Qu F, Morris TJ. HRT gene function requires interaction between a NAC protein and viral capsid protein to confer resistance to turnip crinkle virus. Plant Cell. 2000;12(10):1917–25.
Xia N, Zhang G. YanFei, Zhu L, XU, LiangSheng, CHEN, XianMing, Liu BO. TaNAC8, a novel NAC transcription factor gene in wheat, responds to stripe rust pathogen infection and abiotic stresses. Physiol Mol Plant P. 2010;74(5):394–402.
Wang XB, Zhang H, Li G, Li W, Virk N, Mengiste T, Song F. The Arabidopsis ATAF1, a NAC transcription factor, is a negative regulator of defense responses against necrotrophic fungal and bacterial pathogens. Mol Plant Microbe In. 2009;22(10):1227–38.
Voitsik AM, Muench S, Deising HB, Voll LM. Two recently duplicated maize NAC transcription factor paralogs are induced in response to Colletotrichum graminicola infection. BMC Plant Biol. 2013;13(1):85.
Nakashima K, Tran LS, Van Nguyen D, Fujita M, Maruyama K, Todaka D, Ito Y, Hayashi N, Shinozaki K, Yamaguchi-Shinozaki K. Functional analysis of a NAC-type transcription factor OsNAC6 involved in abiotic and biotic stress-responsive gene expression in rice. Plant J. 2007;51(4):617–30.
Puranik S, Sahu PP, Srivastava PS, Prasad M. NAC proteins: regulation and role in stress tolerance. Trends Plant Sci. 2012;17(6):369–81.
Liu C, Ma H, Zhou J, Li Z, Peng Z, Guo F, Zhang J. TsHD1 and TsNAC1 cooperatively play roles in plant growth and abiotic stress resistance of Thellungiella halophile. Plant J. 2019.
Yu X, Liu Y, Wang S, Tao Y, Wang Z, Shu Y, Peng H, Mijiti A, Wang Z, Zhang H. CarNAC4, a NAC-type chickpea transcription factor conferring enhanced drought and salt stress tolerances in Arabidopsis. Plant Cell Rep. 2015;35(3):1–15.
Huang Q, Wang Y, Li B, Chang J, Chen M, Li K, Yang G, He G. TaNAC29, a NAC transcription factor from wheat, enhances salt and drought tolerance in transgenic Arabidopsis. BMC Plant Biol. 2015;15(1):268.
Yang XW, Wang XY, Ji L, Yi ZL, Fu CX, Ran JC, Hu RB, Zhou GK. Overexpression of a Miscanthus lutarioriparius NAC gene MlNAC5 confers enhanced drought and cold tolerance in Arabidopsis. Plant Cell Rep. 2015;34(6):943.
Honghong H, Mingqiu D, Jialing Y, Benze X, Xianghua L, Qifa Z, Lizhong X. Overexpressing a NAM, ATAF, and CUC (NAC) transcription factor enhances drought resistance and salt tolerance in rice. Proc Natl Acad Sci U S A. 2006;103(35):12987–92.
Hong Y, Zhang H, Huang L, Li D, Song F. Overexpression of a stress-responsive NAC transcription factor gene ONAC022 improves drought and salt tolerance in rice. Front Plant Sci. 2016;7(e0116646):4.
Zheng XN, Chen B, Lu GJ, Han B. Overexpression of a NAC transcription factor enhances rice drought and salt tolerance. Biochem Bioph Res Co. 2009;379(4):985–9.
Jeong JS, Kim YS, Baek KH, Jung H, Ha S, Do Choi Y, Kim M, Reuzeau C, Kim J. Root-specific expression of OsNAC10 improves drought tolerance and grain yield in rice under field drought conditions. Plant Physiol. 2010;153(1):185–97.
Ooka H, Satoh K, Doi K, Nagata T, Otomo Y, Murakami K, Matsubara K, Osato N, Kawai J, Carninci P. Comprehensive analysis of NAC family genes in Oryza sativa and Arabidopsis thaliana. DNA Res. 2003;10(6):239.
Guérin C, Roche J, Allard V, Ravel C, Mouzeyar S, Bouzidi MF. Genome-wide analysis, expansion and expression of the NAC family under drought and heat stresses in bread wheat (T. aestivum L.). PLoS One. 2019;14(3):e213390.
Borrill P, Harrington SA, Uauy C. Genome-wide sequence and expression analysis of the NAC transcription factor family in polyploid wheat. G3-Genes Genom Genet. 2017;7(9):g3–g117.
Liu M, Ma Z, Sun W, Huang L, Wu Q, Tang Z, Bu T, Li C, Chen H. Genome-wide analysis of the NAC transcription factor family in Tartary buckwheat (Fagopyrum tataricum). BMC Genomics. 2019;20(1).
Shiriga K, Sharma R, Kumar K, Yadav SK, Hossain F, Thirunavukkarasu N. Genome-wide identification and expression pattern of drought-responsive members of the NAC family in maize. Meta Gene. 2014;2(1):407–17.
Peng X, Zhao Y, Xiaoming LI, Min WU, Chai W, Sheng L, Wang YU, Dong Q, Jiang H, Cheng B. Genomewide identification, classification and analysis of NAC type gene family in maize. J Genet. 2015;94(3):377.
Puranik S, Sahu PP, Mandal SN, Vs B, Parida SK, Prasad M. Comprehensive genome-wide survey, genomic constitution and expression profiling of the NAC transcription factor family in foxtail millet (Setaria italica L.). PLoS One. 2013;8(5):e64594.
Le DT, Nishiyama R, Watanabe Y, Mochida K, Yamaguchishinozaki K, Shinozaki K, Tran LS. Genome-wide survey and expression analysis of the plant-specific NAC transcription factor family in soybean during development and dehydration stress. DNA Res. 2011;18(4):263–76.
Singh AK, Sharma V, Pal AK, Acharya V, Ahuja PS. Genome-wide organization and expression profiling of the NAC transcription factor family in potato (Solanum tuberosum L.). DNA Res. 2013;20(4):403–23.
Ma J, Wang F, Li MY, Jiang Q, Tan GF, Xiong AS. Genome wide analysis of the NAC transcription factor family in Chinese cabbage to elucidate responses to temperature stress. Sci Hortic-Amsterdam. 2014;165(3):82–90.
Diao W, Snyder JC, Wang S, Liu J, Pan B, Guo G, Ge W, Mhsa D. Genome-wide analyses of the NAC transcription factor gene family in pepper (Capsicum annuum L.): chromosome location, phylogeny, structure, expression patterns, cis-elements in the promoter, and interaction network. Int J Mol Sci. 2018;19(4):1048–61.
Hu W, Wei Y, Xia Z, Yan Y, Hou X, Zou M, Lu C, Wang W, Peng M. Genome-wide identification and expression analysis of the NAC transcription factor family in cassava. PLoS One. 2015;10(8):e136993.
Wei S, Gao L, Zhang Y, Zhang F, Yang X, Huang D. Genome-wide investigation of the NAC transcription factor family in melon ( Cucumis melo L.) and their expression analysis under salt stress. Plant Cell Rep. 2016;35(9):1827–39.
Wu ZY, Xu XQ, Xiong WD, Wu PZ, Chen YP, Li MR, Wu GJ, Jiang HW. Genome-wide analysis of the NAC gene family in physic nut (Jatropha curcas L.). PLoS One. 2015;10(6):124–32.
Su H, Zhang S, Yuan X, Chen C, Wang XF, Hao YJ. Genome-wide analysis and identification of stress-responsive genes of the NAM-ATAF1,2-CUC2 transcription factor family in apple. Plant Physiol Bioch. 2013;71(2):11–21.
Viswanathan S, Jagannadham PTK, Parameswaran C, Jain PK, Srinivasan R. NAC transcription factor genes: genome-wide identification, phylogenetic, motif and cis-regulatory element analysis in pigeonpea (Cajanus cajan (L.) Millsp.). Mol Biol Rep. 2014;41(12):7763–73.
Shi J, Ma X, Zhang J, Zhou Y, Liu M, Huang L, Sun S, Zhang X, Gao X, Zhan W, et al. Chromosome conformation capture resolved near complete genome assembly of broomcorn millet. Nat Commun. 2019;10(1):464.
Zou C, Li L, Miki D, Li D, Tang Q, Xiao L, Rajput S, Deng P, Peng L, Jia W, et al. The genome of broomcorn millet. Nat Commun. 2019;10(1):436.
Wei Y, Shi H, Xia Z, Tie W, Ding Z, Yan Y, Wang W, Hu W, Li K. Genome-wide identification and expression analysis of the WRKY gene family in cassava. Front Plant Sci. 2016;7(2):25.
Nuruzzaman M, Manimekalai R, Sharoni AM, Satoh K, Kondoh H, Ooka H, Kikuchi S. Genome-wide analysis of NAC transcription factor family in rice. Gene. 2010;465(1):30–44.
Ohbayashi I, Lin C, Shinohara N, Matsumura Y, Machida Y, Horiguchi G, Tsukaya H, Sugiyama M. Evidence for a role of ANAC082 as a ribosomal stress response mediator leading to growth defects and developmental alterations in Arabidopsis. Plant Cell. 2017;29(10):255–2017.
Inge DC, Vanessa V, Olivier VA, Klaas V, Murcha MW, Law SR, Annelies I, Sophia N, Aneta I, Debbie R. The membrane-bound NAC transcription factor ANAC013 functions in mitochondrial retrograde regulation of the oxidative stress response in Arabidopsis. Plant Cell. 2013;25(9):3472–90.
Ng S, Ivanova A, Duncan O, Law SR, Van Aken O, De Clercq I, Wang Y, Carrie C, Xu L, Kmiec B. A membrane-bound NAC transcription factor, ANAC017, mediates mitochondrial retrograde signaling in Arabidopsis. Plant Cell. 2013;25(9):3450–71.
Van AO, Pogson BJ. Convergence of mitochondrial and chloroplastic ANAC017/PAP-dependent retrograde signalling pathways and suppression of programmed cell death. Cell Death Differ. 2017;24(6):955.
Wang Y, Tang H, Debarry JD, Tan X, Li J, Wang X, Lee TH, Jin H, Marler B, Guo H, et al. MCScanX: a toolkit for detection and evolutionary analysis of gene synteny and collinearity. Nucleic Acids Res. 2012;40(7):e49.
Li H, Gu M. Breeding of a new broomcorn millet cultivar Jinshu 5 and its cultural practices. Shanxi J Agric Sci. 2002;5:41–2.
Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2-△△CT method. Methods. 2001;25(4):402–8.
We thank Professor Xianmin Diao from the Institute of Crop Science, Chinese Academy of Agricultural Sciences and Professor Ruhong Cheng from the Hebei Academy of Agriculture and Forestry Sciences for their valuable suggestions and useful comments, which have greatly improved the manuscript.
This work was financially supported by the China Agricultural Research System (CARS-06-13.5-A10) and the Fund for Agricultural Science, Technology and Innovation in Hebei, China to GL (2019-4-2-5). The funding bodies played no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Additional file 1: Table S1.
List of the NAC sequences in broomcorn millet. Table S2. Protein property of PmNAC proteins. Table S3. The structural features of motif 1–20. Table S4. Expression (FPKM) of PmNAC genes in different tissues. Table S5. Expression (FPKM) of PmNAC genes in response to drought treatment in broomcorn millet. Table S6. The gene ID of NAC members from Arabidopsis thaliana. Table S7. Sequences of primers used in qRT-PCR.
Rights and permissions
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
About this article
Cite this article
Shan, Z., Jiang, Y., Li, H. et al. Genome-wide analysis of the NAC transcription factor family in broomcorn millet (Panicum miliaceum L.) and expression analysis under drought stress. BMC Genomics 21, 96 (2020). https://doi.org/10.1186/s12864-020-6479-2
- Broomcorn millet
- NAC genes
- Gene expression
- Drought stress