Faulconnier Yannick, Ye Tao, Leroux Christine
INRAE, VetAgro Sup, Université Clermont Auvergne, Saint-Genès-Champanelle, France.
Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Centre National de la Recherche Scientifique, UMR7104, Institut National de la Santé et de la Recherche Médicale, U964, Université´ de Strasbourg, Illkirch, France.
J Anim Sci. 2025 Jan 4;103. doi: 10.1093/jas/skaf044.
One of the main functions of ruminant adipose tissue (AT) is to store lipids for use in productive functions. Body fat mobilization is required during periods of negative energy balance (NEB) such as early lactation or undernutrition. Ruminant nutrition modifies the expression of adipose genes, the regulation of which is not fully understood. The expression of more than 60% of protein-coding genes is post-transcriptionally regulated by microRNAs (miRNAs, small non-coding RNAs, 18 to 25 nucleotides targeting messenger RNAs). Our aim was to characterize miRNA whose expression is regulated by nutrition in the lactating goat AT. Using high-throughput sequencing technology, miRNomes of the lactating AT were established from lactating goats fed a control diet ad libitum and after 48 h of food deprivation (FD) leading to an NEB. MiRNAs sequencing revealed 637 known miRNAs in omental AT of which 16 showed an expression modulated by FD; 14 were upregulated and 2 were downregulated. The network of miRNA-target enrichment identified 2 major miRNAs, miR-223-3p and miR-21-5p which were upregulated by FD and suggested an increase in inflammation of the AT with an NEB obtained after fasting during lactation. The target gene predictions of the differentially expressed miRNAs in AT indicated a significant enrichment in gene ontology functional categories of cell life including apoptosis, cell proliferation, and differentiation as well as in gene expression machinery including regulation of translation and transcription. These data suggest that miRNAs may play a key role in the regulation of AT remodeling.
反刍动物脂肪组织(AT)的主要功能之一是储存脂质以供生产功能使用。在能量负平衡(NEB)期间,如泌乳早期或营养不足时,需要动员体脂。反刍动物营养会改变脂肪基因的表达,但其调控机制尚未完全了解。超过60%的蛋白质编码基因的表达受到微小RNA(miRNA,小的非编码RNA,18至25个核苷酸,靶向信使RNA)的转录后调控。我们的目的是鉴定泌乳山羊AT中受营养调控的miRNA。利用高通量测序技术,从自由采食对照日粮的泌乳山羊以及禁食48小时(FD)导致能量负平衡后的泌乳山羊中建立了泌乳期AT的miRNA组。miRNA测序在网膜AT中发现了637种已知的miRNA,其中16种显示其表达受FD调控;14种上调,2种下调。miRNA-靶标富集网络鉴定出2种主要的miRNA,即miR-223-3p和miR-21-5p,它们在FD后上调,并表明泌乳期禁食后能量负平衡时AT的炎症增加。AT中差异表达的miRNA的靶基因预测表明,在包括细胞凋亡、细胞增殖和分化在内的细胞生命基因本体功能类别以及包括翻译和转录调控在内的基因表达机制中显著富集。这些数据表明,miRNA可能在AT重塑的调控中起关键作用。