Meale S J, Romao J M, He M L, Chaves A V, McAllister T A, Guan L L
Faculty of Veterinary Science, University of Sydney, Sydney, NSW 2006, Australia Lethbridge Research Centre, Agriculture and Agri-Food Canada, Lethbridge, Alberta T1J 4B1, Canada.
Department of Agricultural, Food and Nutritional Science, University of Alberta, Edmonton, AB, Canada.
J Anim Sci. 2014 Aug;92(8):3328-37. doi: 10.2527/jas.2014-7710. Epub 2014 Jun 3.
Knowledge of the molecular mechanisms that regulate ovine adipogenesis is very limited. MicroRNAs (miRNA) have been reported as one of the regulatory mechanisms of adipogenesis. This study aimed to compare the expression of miRNA related to ovine adipogenesis in different adipose depots and to investigate whether their expression is affected by dietary fatty acid composition. We also investigated the role of miRNA in adipogenic gene regulation. Subcutaneous and visceral adipose tissue samples were collected at slaughter from 12 Canadian Arcott lambs fed a barley-based finishing diet where an algae meal (DHA-Gold; Schizochytrium spp.) replaced flax oil and barley grain at 0 or 3% DM (n = 6). Total RNA from each tissue was subjected to quantitative real time (qRT-) PCR analysis to determine the expression of 15 selected miRNA including 11 identified from bovine adipose tissues and 4 conserved between bovine and ovine species. MicroRNAs were differentially expressed according to diet in each tissue depot (miR-142-5p and miR-376d) in visceral and miR-142-5p, miR-92a, and miR-378 in subcutaneous adipose tissue; P ≤ 0.05) and in each tissue depot depending on diet (miR-101, miR-106, miR-136, miR-16b, miR-196a-1, miR-2368*, miR-2454, miR-296, miR-376d, miR-378, and miR-92a in both control and DHA-G diets and miR-478 in control; P ≤ 0.05). Six miRNA were subjected to functional analysis and 3 genes of interest (ACSL1, PPARα, and C/EBPα) were validated by qRT-PCR. Both diet and tissue depot affected expression levels of all 3 genes (P < 0.05). miR-101, miR-106, and miR-136 were negatively correlated with their respective predicted gene targets C/EBPα, PPARα, and ACSL1 in subcutaneous adipose tissue of lambs fed DHA-G. Yet miR-142-5p and miR-101 showed no correlation with ACSL1 or C/EBPα. The variability in expression patterns of miRNA across adipose depots reflects the tissue specific nature of adipogenic regulation. Although the examined miRNA appear to be conserved across ruminant species, our results indicate the presence of ovine specific regulatory mechanisms that can be influenced by diet.
目前对于调控绵羊脂肪生成的分子机制的了解非常有限。据报道,微小RNA(miRNA)是脂肪生成的调控机制之一。本研究旨在比较与绵羊脂肪生成相关的miRNA在不同脂肪库中的表达情况,并探究其表达是否受日粮脂肪酸组成的影响。我们还研究了miRNA在脂肪生成基因调控中的作用。从12只加拿大阿尔科特羔羊屠宰时采集皮下和内脏脂肪组织样本,这些羔羊饲喂以大麦为基础的育肥日粮,其中藻粉(DHA-Gold;裂殖壶菌属)分别以0%或3%的干物质替代亚麻油和大麦谷物(每组n = 6)。对每个组织的总RNA进行定量实时(qRT-)PCR分析,以确定15种选定miRNA的表达,其中包括从牛脂肪组织中鉴定出的11种以及牛和绵羊物种间保守的4种。在每个组织库中,miRNA的表达因日粮不同而存在差异(在内脏脂肪组织中为miR-142-5p和miR-376d,在皮下脂肪组织中为miR-142-5p、miR-92a和miR-378;P≤0.05),并且在每个组织库中也因日粮不同而有所差异(在对照日粮和DHA-G日粮中均有差异的miR-101、miR-106、miR-136、miR-16b、miR-196a-1、miR-2368*、miR-2454、miR-296、miR-376d、miR-378和miR-92a,以及对照日粮中的miR-478;P≤0.05)。对6种miRNA进行了功能分析,并通过qRT-PCR验证了3个感兴趣的基因(ACSL1、PPARα和C/EBPα)。日粮和组织库均影响所有3个基因的表达水平(P < 0.05)。在饲喂DHA-G的羔羊皮下脂肪组织中,miR-101、miR-106和miR-136与其各自预测的基因靶点C/EBPα、PPARα和ACSL1呈负相关。然而,miR-142-5p和miR-101与ACSL1或C/EBPα无相关性。miRNA在不同脂肪库中的表达模式差异反映了脂肪生成调控的组织特异性。尽管所检测的miRNA在反刍动物物种间似乎是保守的,但我们的结果表明存在可受日粮影响的绵羊特异性调控机制。