Adipogenic and energy metabolism gene networks in longissimus lumborum during rapid post-weaning growth in Angus and Angus × Simmental cattle fed high-starch or low-starch diets
© Graugnard et al; licensee BioMed Central Ltd. 2009
Received: 30 December 2008
Accepted: 31 March 2009
Published: 31 March 2009
Transcriptional networks coordinate adipocyte differentiation and energy metabolism in rodents. The level of fiber and starch in diets with adequate energy content fed to young cattle has the potential to alter intramuscular adipose tissue development in skeletal muscle. Post-weaning alterations in gene expression networks driving adipogenesis, lipid filling, and intracellular energy metabolism provide a means to evaluate long-term effects of nutrition on longissimus muscle development across cattle types.
Longissimus lumborum (LL) from Angus (n = 6) and Angus × Simmental (A × S; n = 6) steer calves (155 ± 10 days age) fed isonitrogenous high-starch (HiS; 1.43 Mcal/kg diet dry matter; n = 6) or low-starch (LoS; 1.19 Mcal/kg diet dry matter; n = 6) diets was biopsied at 0, 56, and 112 days of feeding for transcript profiling of 31 genes associated with aspects of adipogenesis and energy metabolism. Intake of dietary energy (9.44 ± 0.57 Mcal/d) across groups during the study did not differ but feed efficiency (weight gain/feed intake) during the first 56 days was greater for steers fed HiS. Expression of PPARG increased ca. 2-fold by day 56 primarily due to HiS in A × S steers. Several potential PPARG-target genes (e.g., ACACA, FASN, FABP4, SCD) increased 2.5-to-25-fold by day 56 across all groups, with responses (e.g., FASN, FABP4) being less pronounced in A × S steers fed LoS. This latter group of steers had markedly greater blood plasma glucose (0.99 vs. 0.79 g/L) and insulin (2.95 vs. 1.17 μg/L) by day 112, all of which were suggestive of insulin resistance. Interactions were observed for FABP4, FASN, GPAM, SCD, and DGAT2, such that feeding A × S steers high-starch and Angus steers low-starch resulted in greater fold-changes by day 56 or 112 (GPAM). Marked up-regulation of INSIG1 (4-to-8-fold) occurred throughout the study across all groups. SREBF1 expression, however, was only greater on day 112 namely due to LoS in A × S steers. The lipogenic transcription factor THRSP was 6-to-60-fold greater by day 56 primarily due to HiS in A × S steers, constituting the greatest response among all genes.
Results involving gene markers of mature adipocytes (e.g., PPARG, THRSP, SCD) provided evidence of intramuscular adipose tissue differentiation during the early portion of the growing phase. The resulting gene networks underscored a central role for PPARG in controlling transcription of genes which are known to co-ordinately regulate adipocyte differentiation and lipid filling in non-ruminants. Unlike rodents, INSIG1 appears to play an important role in cattle muscle adipogenesis. We propose that a network of transcription regulators and nuclear receptors including PPARG-target genes, INSIG1, and THRSP, coordinate activation of adipocyte differentiation and lipid filling at an early age.
Most biological traits are complex, i.e. they are under the control of an interacting network of genes, each with a small effect, and of environmental factors such as nutrition . Metabolic regulation in complex organisms relies partly on transcriptional control as a long-term mechanism affecting the level of expression of key enzymes . In rodents, there is high correlation between mRNA expression of target genes and recruitment of lipogenic transcription factors or nuclear receptors and their co-regulatory proteins to promoter regions, suggesting that gene expression analysis is useful for inferring transcriptional activity . Transcriptional regulation of hepatic lipogenic gene expression, adipogenesis, and skeletal muscle fatty acid oxidation in rodents is under control of sterol regulatory element binding factor 1 (SREBF1)  and the ligand-activated nuclear receptors PPARγ (PPARG) and PPARδ (PPARD) [5, 6]. Less is known regarding the molecular events during skeletal muscle growth in livestock species such as cattle and pigs . However, recent work has begun to explore large-scale transcriptomic adaptations in skeletal muscle of cattle in response to plane of nutrition (e.g., normal vs. underfeeding) or age [8–11]. Although mRNA expression is one of multiple factors to be considered when studying the complex molecular networks working simultaneously in tissues of varying cell types (e.g., myocytes, non-differentiated stem cells, pre-adipocytes, adipocytes ) like skeletal muscle, it provides valid information to aid in designing more detailed functional studies.
Young steer calves are relatively more efficient at converting nutrients to muscle gain [12, 13]. Weaning calves at an earlier age than the conventional 205 days is a management practice that has shown to enhance growth rate, modify carcass composition, and modify meat quality [14–16]. Exposing them to high-starch diets at an early vs. conventional age could increase the likelihood that they reach their genetic potential to marble (i.e., deposit intramuscular fat). To our knowledge, no studies have been conducted to examine the influence of dietary starch level at an early age on gene networks regulating pivotal pathways for desired phenotypes of economically-important traits. High-starch/low-fiber diets, through shifting the pattern of end-products of ruminal fermentation towards greater propionate, provide readily-available sources of energy (i.e., glucose) for growing muscle in early-weaning management systems [12, 13]. A previous study with early-weaned Angus × Simmental steers reported greater intramuscular fat and backfat thickness at the end of the growing phase in animals fed a high-starch vs. high-fiber diet . Energy available for gain was ca. 35% greater in steers fed the high-starch diet, which undoubtedly contributed to enhanced fat deposition.
Description of genes analyzed in skeletal muscle tissue.
Fatty acid biosynthesis
Citrate metabolic process
Plasma and ER membranes
Fatty acid metabolism
Phosphatidic acid biosynthesis
Fatty acid metabolism
Fatty acid binding, transport
Unsaturated fatty acid synthesis
Fatty acid biosynthesis
Lipid metabolism, cell proliferation
Insulin receptor signaling
Insulin receptor signaling
Nucleus, ER, cytosol
Phosphatidic acid hydrolysis, transcription
Phosphatidic acid hydrolysis
Phosphatidic acid hydrolysis
Tricarboxylic acid cycle, malate metabolic process
Fatty acid beta-oxidation, transcription
Induction of adipocyte differentiation, transcription
Fatty acid beta-oxidation, transcription factor
DNA-dependent regulation of transcription
Fatty acid biosynthesis, signal transduction
Fatty acid biosynthesis, signal transduction
ER membrane, Golgi
SREBP target gene transcription activation
Fatty acid biosynthesis
Plasma and ER membranes
Fatty acid transport
Plasma membrane, cytosol
Glucose transport, glucose homeostasis
Golgi and ER membranes, nucleus
Lipid metabolic process
Results and discussion
A primary objective was to manipulate the profile of ruminal fermentation products (e.g., increase propionate) through feeding diets with different levels of starch and fiber. Classical studies showed that intravenous infusions (14-day) of propionate or glucose (relative to saline, acetate, or lactate) into steers promoted greater in vitro incorporation of glucose, acetate, and lactate into subcutaneous adipose tissue lipid . This response was accompanied by greater fatty acid synthetase (FASN), acetyl-CoA carboxylase-α (ACACA), and ATP-citrate lyase (ACLY), as well as unchanged malate dehydrogenase 2, NAD (mitochondrial) (MDH2) activity primarily when glucose was infused. The relative potency of substrates for inducing lipogenesis in ruminant adipose tissue was proposed to be glucose > propionate ≥ lactate > acetate .
Despite the well-defined greater rates of lipogenesis in subcutaneous adipose tissue of cattle , work also has shown greater intramuscular adipose FASN activity in 16–18 month-old steers fed high-starch (i.e., corn grain) vs. low-starch diets (i.e., corn silage) . Intramuscular adipose tissue from steers fed the high-starch diet incorporated more glucose than acetate into glyceride-fatty acids and this response was augmented by age . Due to gluconeogenesis in liver, both propionate and lactate can indirectly modulate adipose tissue lipogenesis through increased glucose synthesis, availability, or both. The glucogenic effect of high-starch diets is often accompanied by an enhanced insulin response , a well-known adipogenic/lipogenic signal in rodents . There is some indication, however, that insulin in mature cattle is not as effective in increasing in vivo rates of lipogenesis in subcutaneous adipose as it is in rodents . The responsiveness to insulin and abundance of insulin receptors increases dramatically as preadipocytes undergo terminal differentiation into adipocytes .
Animal performance in response to a high-starch (HiS) or low-starch (LoS) diet during a 112-d growing phase.
A × S
A × S
Diet × Steer type
Body weight (kg)
Initial, d 0
Final, d 112
0 to 56 d
56 to 112 d
0 to 112 d
Dry matter intake (kg/day)
0 to 56 d
56 to 112 d
0 to 112 d
NEG intake (Mcal/day)1
0 to 56 d
56 to 112 d
0 to 112 d
Residual feed intake
Feed efficiency2 (kg/kg)4
0 to 56 d
56 to 112 d
0 to 112 d
Day 112 ultrasound
Back fat (mm)
Muscle depth (mm)
Performance responses, including feed intake, energy intake, and residual feed intake from the subset of steers used for transcript profiling was comparable to the whole group of animals in the entire experiment (Additional File 1) suggesting that the steers randomly chosen for transcript profiling were representative of the entire group. Furthermore, each steer served as its own control because of the repeated sampling over time. Similar approaches for transcript profiling studies of skeletal muscle tissue have been used previously [8, 11].
Previously, high-starch vs. low-starch diets fed to early-weaned A × S steers (n = 19–20/diet) for 100 days resulted in moderately greater intramuscular fat (3.6% vs. 3.2%) measured via ultrasound . Our steers fed LoS, however, consumed greater overall amounts of energy than those fed LoS in the study of Schoonmaker et al. . We were unable to obtain reliable measurements of marbling at 56 days of feeding but mRNA expression data discussed in the subsequent sections is indicative of diet effects on adipogenesis and lipid filling. Because the vast majority of metabolic enzymes in mammals are regulated at the transcriptional level , measurement of mRNA for multiple genes and their networks in a pathway should expand our understanding of muscle and fat development  in response to nutrition, genotype, and their interaction [9, 11].
Transcriptional regulatory networks of adipogenesis in LL
Several growth factors in blood such as insulin, insulin-like growth factor-1 (IGF-I), growth hormone, thyroid hormones (i.e., triiodothyronine), as well as vitamins , are required to stimulate proliferation of pre-adipocytes . Classical studies in cattle demonstrated subcutaneous adipocyte hyperplasia between 4 and 7 months of age , and between 11 and 17 months of age . There also are well-defined age-related increases in subcutaneous adipose ACLY, glucose-6-phosphate dehydrogenase (G6PD), ACACA, and FASN activity in growing crossbred steers fed high-starch vs. low-starch diets, which correlated with in vitro lactate and acetate incorporation into lipid [19, 23]. During rapid post-weaning growth it is possible that a population of pre-adipocytes exits the proliferative phase and enters terminal differentiation .
PPARG role in marbling deposition could be crucial because in non-ruminants most pro-adipogenic factors seem to function at least in part by activating PPARγ expression or activity . Up-regulation of PPARγ is sufficient to induce adipocyte differentiation in vitro and no factor has been discovered that promotes adipogenesis in the absence of PPARγ . Terminal differentiation of adipocytes requires up-regulation of mRNA of fatty acid binding protein 4 (FABP4), G6PD, FASN, and ACACA, among others, which are under the control of PPARγ [7, 28]. Additional PPARG-target genes [7, 22] analyzed in the present study included: ACLY, CD36 molecule [thrombospondin receptor] (CD36), diacylglycerol O-acyltransferase homolog 1 and 2 (DGAT1 and 2), stearoyl-CoA desaturase (SCD), mitochondrial glycerol-3-phosphate acyltransferase (GPAM), insulin induced gene 1 (INSIG1), insulin receptor (INSR), insulin receptor substrate 1 (IRS1), solute carrier family 2 [facilitated glucose transporter] member 4 (SLC2A4), solute carrier family 27 [fatty acid transporter] member 1 (SLC27A1), and sterol regulatory element binding transcription factor 1 (SREBF1).
Among all potential PPARγ target genes, we found a highly-positive and significant correlation between FABP4 and PPARG regardless of steer type or diet (Additional File 2) which is suggestive of an increase in PPARγ activity. We recently presented direct evidence, via use of the PPARγ agonist rosiglitazone, that SREBF1, FASN, ACACA and potentially FABP4 and thyroid hormone responsive (SPOT14 homolog, rat) (THRSP) are PPARG target genes in the bovine . Some of the above genes remained elevated through day 112 regardless of diet or steer type. Along with PPARG, the expression patterns of FASN, FABP4, SCD, ACLY, THRSP, and DGAT2 clustered together into the most up-regulated group of genes (Additional File 1). This observation together with the correlation data (Additional File 2) for FASN, SCD, ACLY, and DGAT2 with PPARG, in particular, provides additional evidence that they likely are PPARG downstream genes in cattle. Considering the essential role of PPARγ in adipogenesis , we speculate that these genes could be considered an essential subset for adipocyte differentiation and lipid filling. Previous work showed intramuscular adipocyte hyperplasia (i.e., proliferation) occurring at 11 through 17 months of age . Increased adipocyte number in our study encompassing steers ca. 4–8 months of age is supported by some of the measured genes which are highly abundant in adipose compared with other tissues in mammals (e.g. PPARG, DGAT2, FABP4, SCD; ), and also by the increase in total fatty acid concentration in muscle tissue over time (Additional File 1).
We observed interaction effects (including tendencies) on the mRNA expression patterns of FABP4, ACLY, FASN, SCD, GPAM, and DGAT2. Hierarchical clustering analysis clearly highlighted differences in expression of these genes across steer type and diet combinations (Additional File 1). All these genes had the opposite response between steer types when fed the two diets particularly on day 56, e.g., feeding HiS to A × S steers resulted in the greatest response compared with A × S steers fed LoS. Also, Angus steers responded with greater values for most of these genes when LoS was fed (Figures 3, 4). There was a clear time effect on all the lipogenic genes (e.g., ACACA, FASN, SCD) with peak expression at 56 days and a moderate decrease thereafter. At 112 days, few of these genes had significant differences between groups, with an overall tendency for Angus steers to have greater values. In general, these data agree with marbling scores measured at 112 days showing greater responses in Angus steers.
The common trend for decreased mRNA expression after 56 days seems to suggest that the initial adipogenic response through 56 days did not influence intramuscular fat deposition by 112 days. There is evidence of positive correlations between mRNA expression of certain lipogenic genes/transcription regulators and intramuscular fat content in crossbred cattle . However, it was intriguing that A × S steers fed HiS, with numerically lower marbling score at day 112, had the same pattern of expression among all adipogenic genes compared with Angus steers fed LoS, which in the end had numerically greater marbling scores. It also is noteworthy that A × S steers fed LoS had lower temporal expression of most genes driving adipogenesis (Figure 2, 3, 4) without discernable effects on marbling scores. Potential carry-over effects of high-starch diets on intramuscular fat content need to be evaluated during the finishing phase and/or at slaughter.
SREBP1 is a pro-adipogenic factor regulating transcriptional cascades primarily in rodent liver . The transcription factor binds specific DNA domains  eliciting transcription of genes involved in lipid and cholesterol metabolism. A direct crosstalk with PPARγ or via generation of a lipid PPARγ-ligand whose identity is still unknown has been proposed as an additional mechanism during adipocyte differentiation . We have evidence that SREBF1 is a PPARγ-target gene in bovine cells . The role of SREBP1c on lipid homeostasis in rodent cells/tissues (primarily hepatocytes) has been well-established [7, 32]. At normal levels of expression in murine liver, SREBP1c activates expression of ACLY, G6PD, ACACA, FASN, SCD, and GPAM leading to synthesis of palmitic acid, oleic acid, and formation of triacylglycerol (TAG) . Similar responses have been reported in murine adipose tissue . Recent data, however, casts some doubt on the essentiality of SREBP1 for regulation of rodent adipocyte lipogenic gene expression .
In our study, mRNA of SREBF1 was significantly greater between 56 and 112 days in all groups except A × S steers fed HiS (Figure 2). mRNA of INSIG1 had greater up-regulation by 56 days and remained elevated through 112 days in all groups except A × S steers fed HiS. The overall increase in expression of SREBF1, at least through the second portion of the feeding phase, is additional indication of an enrichment  of intramuscular adipocytes. Induction of adipogenesis in bovine bone marrow stromal cells led to greater SREBF1 mRNA several days after they were induced to differentiate . It could be possible that changes in SREBF1 expression exert some level of control over intramuscular lipogenesis in growing cattle, but the substantial and sustained increase in expression of INSIG1 along with its high mRNA abundance relative to SREBF1 (Additional File 1) are indicative of low activity of SREBP1. Furthermore, a recent study in rodents found that lipogenic gene expression in adipose tissue was independent of SREBP1 . Together, these observations cast doubt on the essentiality of this transcription factor in cattle intramuscular fat accumulation.
INSIG1 mRNA in murine adipose tissue is induced by activation of PPARγ but it occurs relatively late in the adipogenic program, preceded by peak of PPARG and SREBF1 mRNA expression . In fact, both PPARG and SREBF1 activate transcription of INSIG1 and regulate its expression during adipogenesis . The primary function of INSIG1 in adipose tissue or liver is to block processing of SREBP1 . However, it is believed that concomitant increase in the activation of INSIG1 and SREBP1 is a counterbalance mechanism ("brake") to prevent uncontrolled SREBP1 action, i.e. lipogenesis [33, 37]. Up-regulation of INSIG1 transcription in adipocytes effectively down-regulated expression of PPARG and SREBF1, essentially blocking differentiation of pre-adipocytes . Thus, an increase in expression of INSIG1 provides a feedback signaling mechanism to restrict both lipogenesis and adipogenesis. Our data, however, do not seem to support such a mechanism in bovine muscle because the response in INSIG1 expression was greater in Angus steers, which had greater marbling scores at 112 days. In addition, Angus steers fed LoS had the greatest increase in expression of INSIG1 as well as numerically highest marbling scores and total fatty acids in muscle tissue (Additional File 1). INSIG1 is a PPARγ target gene in the mouse  and previous data from our laboratory provided evidence of the same in the bovine . These findings point to a crucial role for PPARγ in controlling intramuscular lipogenesis in cattle. The pattern of INSIG1 expression together with its apparent regulation via PPARγ suggest that this gene might be a pro-lipogenic rather than anti-lipogenic factor as inferred in the mouse .
THRSP is another important gene during adipocyte differentiation in rodents and is partly regulated by thyroid hormone [28, 38, 39]. In rodents, thyroid hormone exerts sustained up-regulation of THRSP expression [28, 38, 39] and can by itself increase rates of lipogenesis in rodent adipose tissue. Both insulin and thyroid hormone can act synergistically in promoting the overall process of adipogenesis in rodents . In pigs, however, it is believed that thyroid hormone acts synergistically with other growth factors such as insulin-like growth factor-I to promote adipocyte differentiation . A microarray study previously identified THRSP, in addition to SCD, FABP4, and SREBF1, as one marker gene preferentially expressed in LL of Japanese Black vs. Holstein steers . The former are widely-known to possess extremely high capacity for marbling. More recently, THRSP mRNA in LL was highly correlated (0.94) with intramuscular fat content in high-marbling Wagyu × Hereford but not in low-marbling Piedmontese × Hereford heifers . Both thyroid hormone and insulin are positively and significantly correlated with feed intake, body weight, and average daily gain in cattle . Insulin and high-carbohydrate diets induced THRSP mRNA in rodent liver  and adipose tissue .
Among novel results, we observed dramatic up-regulation by day 56 of THRSP transcription (Figure 2). A recent study reported marked THRSP in LL of crossbred Wagyu × Hereford vs. Piedmontese × Hereford heifers but at 25 to 30 months of age relative to 3 months of age . The former had greater (10.7% vs. 5.3%) carcass intramuscular fat at slaughter. In our study, the increase in THRSP was not affected by dietary starch in Angus steers while in A × S steers fed HiS it resulted in a tremendous up-regulation of its mRNA abundance. As observed for classical adipogenic genes, A × S steers fed LoS had greater THRSP expression by 56 days but the magnitude of increase was lower compared with other groups. By 112 days, THRSP expression was only numerically greater compared to the pre-experimental value. In other groups, mRNA abundance of THRSP was maintained at >15-fold through day 112 compared with day 0. Insulin and thyroid hormone act synergistically to enhance THRSP-driven lipogenesis in rodent adipose, a mechanism that seems to be in line with the well-defined parallel increases in blood insulin and thyroid hormone during rapid growth in cattle [21, 42]. We found positive correlations between both insulin and glucose with THRSP expression but only in Angus cattle regardless of diet (Additional File 2). For the most part, correlations between mRNA abundance of THRSP and expression of lipogenic genes and PPARG were positive and significant regardless of diet or steer type (Additional File 2). More detailed studies will have to be conducted in the future to determine the role, if any, of thyroid hormone alone or in combination with other hormones or growth factors in the process of adipogenesis during rapid cattle growth.
Despite the well-defined effect of thyroid hormone on rodent lipogenesis it also down-regulates SREBF1 mRNA expression, both in mouse liver  and human adipose tissue . This effect might partly explain the contrasting expression patterns of SREBF1 and THRSP in A × S steers (Figure 2). Sustained up-regulation in expression of THRSP in LL of growing cattle would partly overcome the need for SREBF1 expression and activation of lipogenesis because ACACA and THRSP, at least in murine liver, are co-expressed  thus, THRSP regulation of ACACA in muscle cannot be discounted.
Insulin signaling in LL inferred by gene expression, blood metabolites, and insulin
Short-term in vitro studies with bovine myogenic cells have demonstrated greater INSR and IRS1 protein, marked phosphorylation of IRS1, as well as greater protein of downstream effectors (phosphoinositide-3-kinase,SLC2A4) within minutes of insulin stimulation [45, 46]. Insulin effectively stimulates muscle glucose oxidation and adipogenesis [22, 47], partly through up-regulation of IRS1 transcription  and through activation of downstream signaling cascades including transcription factors (SREBF1), nuclear receptors (e.g., PPARG, PPARGC), and their gene targets (e.g., FABP4, FASN).
Among INSR and IRS1, only the latter had an overall temporal increase in expression, with a pattern similar in all groups except Angus steers fed LoS, which had a decrease in expression throughout the study (Figure 3). The greater temporal expression pattern of SLC2A4was significant only for A × S steers fed LoS. Both, IRS1 (~7% of total genes; Additional File 1) and SLC2A4 (~8% of total genes) were among the most abundant genes measured in our experiment, suggesting an important role in LL. Among isoforms of IRS, expression of IRS1 appears essential for the induction of adipogenesis mediated by insulin in rodents . The pattern of expression of IRS1 in our experiment does not support such a role for this gene in cattle LL. Angus steers fed LoS, which at 112 days had numerically greater marbling score (Table 2) and total fatty acids in muscle tissue (Additional File 1), had the lowest increase in expression of IRS1 and lowest plasma insulin. The low insulin together with low glucose in LoS-fed Angus indicates that they were more insulin sensitive. The opposite was observed for A × S steers fed LoS, which had the lowest numerical marbling score (Table 2) and lowest increase in expression of lipogenic genes despite having the largest increase in expression of IRS1. These results seem to cast doubt on an essential role of IRS1 in adipogenesis/lipogenesis.
The importance of adipose PPARγ to maintain systemic (muscle and adipose) insulin sensitivity in non-ruminants has been convincingly demonstrated . Blood insulin and glucose were clearly greater in A × S steers fed LoS, particularly during the second half of the growing phase (Figure 1), which could be taken as an indication of reduced insulin sensitivity. These cattle were unique because they consumed the greatest amounts of dry matter and energy but their growth and feed conversion efficiency rates did not differ substantially from other animals (Table 2; Additional File 1). Clustering analysis of gene expression patterns underscored the marked differences in mRNA expression induced by feeding a low-starch diet to these animals (Additional File 1). Insulin resistance in A × S steers fed LoS also is supported by the lower temporal response of PPARG-target genes (e.g., ACACA, FABP4) pointing to lower activity of PPARγ, which could be caused by reduced insulin signaling.
The above data are intriguing and, to some extent, counterintuitive. Low-starch diets should not reduce insulin sensitivity as suggested by data from Angus steers in which feeding LoS led to lower plasma insulin. However, results with A × S steers fed LoS agree with a previous study showing that intramuscular fat tissue from steers fed a low- vs. high-starch diet was less sensitive to insulin-stimulated glucose use for lipogenesis . An insulin-resistant state in A × S steers fed LoS can partly help explain the lack of response in expression of adipogenic genes ACACA, FASN, FABP4, GPAM, and DGAT2 throughout the study (Figure 3, 4; Additional File 1) despite greater overall fold-change in SREBF1 mRNA at 112 days (Figure 2; Additional File 1). Transcriptional regulation of SREBF1 in most non-ruminant models is sensitive to insulin, which under times of carbohydrate excess leads to stimulation of fatty acid synthesis and TAG deposition both in adipose  and liver . The decrease in insulin sensitivity also may explain the lower expression of THRSP in A × S steers fed LoS, because insulin is essential for its full expression . Overall, our data suggest that low-starch diets induced insulin resistance in LL of A × S steers and highlights a difference in response to diet between pure bred and crossbred cattle. Further research with greater number of cattle seems warranted to examine more directly insulin sensitivity in LL under these or similar nutritional management schemes.
Intracellular LL tissue energy metabolism
Nuclear receptors and co-activators involved in energy metabolism
During rapid muscle growth the energetic costs associated with protein deposition and intramuscular lipogenesis in LL tissue are expected to increase, as shown by enzymatic activity measurements over time [9, 19, 23]. PPARD is a poorly-studied nuclear receptor with a potentially important role in skeletal muscle energy metabolism. PPARD mRNA is several fold more abundant than PPARα in murine skeletal muscle and effectively performs the same function, i.e. activation of fatty acid oxidation . The co-activators peroxisome proliferator activated receptor coactivator-1α (PPARGC1A) and -1β (PPARGC1B) also are involved in stimulating oxidative metabolism in skeletal muscle . Only Angus steers fed LoS had a significant increase in transcript abundance of PPARD (Additional File 1). PPARGC1A was characterized by a blunted temporal response in all groups except Angus steers fed HiS, which had a large increase by 112 days (Additional File 1). PPARGC1B was consistently up-regulated in steers fed HiS (Additional File 1). We found a positive correlation (except in Angus steers fed LoS) between both PPARGC1A and PPARGC1B with ACSL1, encoding a protein showing to channel fatty acids towards oxidation in heart muscle tissue . ACSL1 had a significant increase in expression over time in all groups except Angus steers fed LoS (Figure 4).
The role of ACSL1 in fatty acid oxidation is likely confounded in our study because in adipose tissue this protein channels fatty acids toward synthesis of TAG, while in muscle it channels fatty acid toward oxidation . The core biopsy tissue in our experiment contained both adipocytes and muscle cells. However, the blunted response in expression of this gene in Angus fed LoS, with greater marbling score, are suggestive of a more prominent role for ACSL1 in channeling fatty acids toward oxidation in cattle muscle cells. This is supported by the positive correlation between ACSL1 with PPARGC isoforms .
Activation of PPARD in vitro has been associated with increased fatty acid oxidation through an AMPK-dependent mechanism . AMPK is a heterodymeric enzyme that functions as an intracellular "fuel gauge" that monitors changes in energy status, and it is activated upon an increase in AMP/ATP ratio essentially reducing anabolic pathways such as lipogenesis . The catalytic subunits of AMPK are encoded by protein kinase, AMP-activated, alpha 1 and 2 catalytic subunits (PRKAA1 and PRKAA2). These two genes did not respond to dietary starch (Additional File 1). Interestingly, PRKAA2 expression within each steer type had the opposite pattern compared with PPARD. Furthermore, PRKAA2 expression during the study increased only in A × S steers but not in Angus.
Angus steers fed LoS had a greater increase in expression of PPARD and numerically greater increase in expression of PRKAA1 compared with feeding HiS (Additional File 1). This might suggest that feeding LoS resulted in greater utilization of preformed fatty acids for oxidation through greater expression of PRKAA1. Increasing fatty acid oxidation would be a means to spare glucose for de novo fatty acid synthesis in intramuscular adipose tissue. This suggestion is supported by the temporal expression of ACLY in Angus steers fed LoS. In fact, this group had greater increase in expression of FASN by 56 days and greater concentrations of short-chain fatty acids in LL tissue (Additional File 1). This mechanism in Angus steers fed LoS is supported only by PPARD data, while remaining genes potentially involved in fatty acid oxidation (e.g., PPARGC1A and B, ACSL1) seem to indicate lower oxidation of fatty acids. A factor that confounds interpretation, as indicated above, is the different composition of cells (i.e., adipocytes, muscle cells) in the core biopsy tissue. Greater expression of ACSL1 is sometimes associated with insulin resistance due to direct effects of long-chain fatty acyl-CoA . An increase in the intracellular pool of long-chain fatty acyl-CoA in A × S steers fed LoS is supported by the sustained up-regulation in CD36 (discussed below; Additional File 1) and up-regulation of SLC27A1 by day 112. Both proteins are involved in uptake of preformed long-chain fatty acids .
Intracellular energy sensors and insulin action
A hallmark of normal tissue insulin signaling is the enhanced uptake of long-chain fatty acids through both passive diffusion as well as protein-mediated transport . The fatty acid translocase FAT/CD36 plays a major role in this process . Both, contraction and insulin appear to up-regulate muscle CD36 recruitment from intracellular stores to the plasma membrane at least in part through the action of AMPK . Longitudinal mRNA expression and mRNA abundance of CD36 and PRKAA2 were greater in A × S steers regardless of diet, and essentially followed the opposite pattern relative to Angus steers (Additional File 1). Both genes exhibited the clearest effect of steer type on transcript expression among the 31 genes examined and their expression clustered together (Additional File 1). Studies have shown that null mutation of CD36 in mouse skeletal muscle leads to impaired AMPK-stimulated (measured via PRKAA2 phosphorylation state) fatty acid oxidation in oxidative fibers . Those previous results would imply that lower CD36 and PRKAA2 mRNA expression in Angus steers potentially serves as a mechanism to divert more long-chain fatty acids taken up via SLC27A1 (greater in Angus steers; Additional File 1) towards TAG synthesis.
It could be possible that CD36 and PRKAA2 work in concert with LPIN isoforms or as yet unidentified nuclear receptors to regulate cellular fatty acid oxidation . The lipin 1 isoform (LPIN1) was shown to selectively activate a subset of PPARGC1A-target pathways, including fatty acid oxidation and mitochondrial oxidative phosphorylation in murine liver . In our data, LPIN2 expression was positively correlated with insulin in both Angus and A × S steers fed HiS, suggesting that it might be associated with adipogenesis.
More functional studies are clearly needed to determine whether up-regulation in expression of transcription factors and nuclear receptors via diet at an early age can induce precocious adipocyte differentiation and ultimately determine intramuscular fat deposition in the carcass. There will be a need for dissecting intramuscular adipose and muscle tissue so that cell-specific analysis can be made. Other limitations of the study were the lack of additional functional data (e.g., measurement of oxidation or TAG synthesis), and actual carcass data. Despite those limitations, our data provided novel insights into longissimus lumborum energy sensing and lipogenic gene networks as affected by dietary starch level and genotype.
Experimental animals and management, diets, and sampling
The study utilized a subset of 12 animals selected from a larger study encompassing 29 early-weaned (134 ± 10 day age at weaning) purebred Angus (n = 17) and Angus × Simmental (n = 12) steers from the University of Illinois beef cattle herd. After a 3-week adjustment period in which all steers were fed the same corn silage-based diet (850 g/kg corn silage and 150 g/kg wet distiller's grains, as-fed basis), 6 Angus and 6 A × S steers from the larger groups that were fed a high-starch (1.43 Mcal/kg diet dry matter; n = 3/steer type) or low-starch (1.19 Mcal/kg diet dry matter; n = 3/steer type) diet for 112 days after weaning (i.e., growing phase) were chosen randomly for LL biopsies. Dietary treatments in this study were specifically designed to provide contrasting levels of starch and fiber while providing sufficient energy, i.e. calculated net energy of gain in diets HiS and LoS differed by ca. 20% but was adequate in both cases to support ≥ 1.5 kg body weight per day . Both diets were formulated to be isonitrogenous. The low-starch/high-fiber diet contained (g/kg dry matter) 350 corn silage, 200 corn gluten feed, 380 soyhulls, 30 cracked corn, and 30 soybean meal (490 g/kg crude protein). The high-starch/low-fiber diet contained (g/kg dry matter) 200 corn silage, 680 cracked corn, and 110 soybean meal (490 g/kg crude protein). Both diets contained (g/kg dry matter) 10 limestone/dicalcium phosphate/mineral/vitamin/urea/dry molasses mixture. Calculated dietary fiber content was 5.9% with HiS and 24% with LoS. Calculated NEG for the low-starch/high-fiber diet was 1.19 Mcal/kg dry matter and 1.43 Mcal/kg dry matter for the high-starch/low-fiber diet. All diets were offered on an ad libitum basis. Steers had an individual electronic identification ear tag, and individual feed intake data were collected using the GrowSafe® system (GrowSafe Systems Ltd., Alberta, Canada). Residual feed intake was calculated by regression  of actual dry matter intake against average metabolic body weight (body weight0.75) and average daily gain (ADG).
Steer weights were recorded on consecutive days before, 56, and 112 days after the start of treatments (i.e., 155 ± 10 day age). Individual-animal ADG and daily dry matter intake were used to estimate feed conversion efficiency (gain/feed, kg/kg; Table 2). Ultrasound images of LL area were captured at 112 days of the growing phase using a 500 V Aloka (Corometrics Medical Systems, Inc., Wallingford, CT) ultrasound with a 3.5-MHz transducer fitted to a custom beef animal standoff. Data were analyzed with AUSkey System Software (Animal Ultrasound Services, Ithaca, NY). Commercial vegetable oil was applied to the site of measurement to decrease sound wave attenuation associated with hair coat.
Blood serum metabolites were analyzed following standard protocols at the Veterinary Diagnostics Laboratory, College of Veterinary Medicine, University of Illinois. Serum insulin concentration was quantified using a commercial bovine insulin ELISA kit (cat# 10-1201-01, Mercodia AB, Uppsala, Sweden).
Muscle biopsies were collected at 0, 56, and 112 days relative to the start of feeding treatment diets (i.e., 155 ± 10 day age) under a protocol (#05095) approved by the University of Illinois Animal Care and Use Committee. Specific details of the biopsy procedures can be found in Additional file 1.
RNA extraction, RNA quality assessment, real time quantitative PCR (qPCR), primer design and evaluation, sequencing, internal control gene (ICG) evaluation, and muscle tissue fatty acid analysis
Specific details of these procedures are presented in Additional File 1. Special attention was given to the selection and evaluation of ICG for normalization of qPCR data. Briefly, microarray data from LL muscle  were mined to select potential ICG (Additional File 1) using established protocols from our laboratories [65–67]. Genes selected from the microarray data which had a stable expression ratio (i.e., 1.0 ± 0.2; sample/reference) included arrestin domain containing 1 (ARRDC1), endothelial differentiation, sphingolipid G-protein-coupled receptor, 1 (EDG1), chromosome 20 open reading frame 196 (C20ORF196), single stranded interacting protein 2 (RBMS2), and mitochondrial GTPase 1 homolog (MTG1). Previously-used [8, 68, 69] genes for normalization of cattle skeletal muscle tissue include actin beta (ACTB), glycerol-3-phosphate dehydrogenase (GAPDH), and cyclophilin (PPIA, PPIB). These transcripts were highly unstable (Additional File 1) and would have been rejected from subsequent analysis based on our initial criteria above. To the 5 genes were included ribosomal protein S15a (RPS15A) and ubiquitously-expressed transcript (UXT), which were previously identified as suitable ICG in bovine mammary tissue , and also ACTB and GAPDH. Absence of co-regulation among these selected genes was evaluated through Ingenuity Pathway Analysis® (Additional File 1). Expression stability was evaluated using geNorm software http://medgen.ugent.be/~jvdesomp/genorm/ following the procedures of Vandesompele et al.  described in Additional File 1. A similar approach was used recently with gene expression data from cattle muscle . Genes selected as ICG based on absence of co-regulation (Additional File 1) and geNorm analysis (Additional File 1) included RBMS2, RPS15A, UXT, and MTG1. The geometric mean of these 4 genes was used to normalize gene expression data in the present study.
Growth performance, blood metabolites and insulin, LL fatty acid concentration, and qPCR data were analyzed as a factorial experiment, with diet and time as the two factors, using the MIXED procedure in SAS (SAS Institute) with repeated measures . Prior to statistical analysis, normalized qPCR data were transformed [73, 74] to fold-change relative to day 0 (i.e., before animals were started on experimental diets). To estimate standard errors at day 0 and prevent biases in statistical analysis, normalized qPCR data were transformed to obtain a perfect mean of 1.0 at day 0, leaving the proportional difference between the biological replicate. The same proportional change was calculated at all other time points to obtain a fold-change relative to day 0. Fixed effects in the statistical model for each variable analyzed (i.e., genes, blood metabolites, performance) included diet, steer type, days on experiment, diet × steer type, diet × days on experiment, steer type × days on experiment, and diet × steer type × days on experiment. Random effect was steer within diet. An autoregressive covariate structure was used . All means were compared using the PDIFF statement of SAS. Significance was declared at P ≤ 0.06. Pearson correlations among genes and performance variables within steer type and diet combination were obtained using the CORR procedure in SAS (Additional File 2).
Hierarchical (Additional File 1) and k-means (Additional File 1) clustering was performed using fold-changes in mRNA expression for each steer type and diet combination on day 56 and day 112 relative to day 0 using Genesis software .
Gene network analysis
Summary networks among genes (Figure 5; Additional File 1) were developed using the web-based software package Ingenuity Pathway Analysis® (http://www.ingenuity.com; Redwood City, CA). The networks were generated using the respective gene identifiers and not the actual fold-changes in expression which are already depicted in Figure 2, 3, and 4. Connections among genes were based on known relationships available in the Ingenuity Pathway Analysis® knowledge based. This is a proprietary manually-curated database containing relationships from the published literature in rodents and humans.
average daily gain
- A × S:
Angus × Simmental steers
real-time quantitative PCR
We gratefully acknowledge the help from T. G. Nash and J. Dahlquist as well as the rest of the staff at the University of Illinois Beef Cattle Unit for animal handling and care.
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