Li Xin, Xing Shan-Shan, Meng Sheng-Bo, Hou Zhong-Yi, Yu Lei, Chen Meng-Juan, Yuan Dong-Dong, Xu Hui-Fen, Cai Han-Fang, Li Ming
College of Animal Science and Technology, Henan Agricultural University, Zhengzhou, China.
Epigenetics. 2024 Dec;19(1):2341578. doi: 10.1080/15592294.2024.2341578. Epub 2024 Apr 14.
Long non-coding RNAs (lncRNAs) have been shown to be involved in the regulation of skeletal muscle development through multiple mechanisms. The present study revealed that the (SRY-box transcription factor 6 antisense upstream) is reverse transcribed from upstream of the bovine sex-determining region Y (SRY)-related high-mobility-group box 6 () gene. was significantly differentially expressed in muscle tissue among different developmental stages in Xianan cattle. Subsequently, knockdown and overexpression experiments discovered that promoted primary skeletal muscle cells proliferation, apoptosis, and differentiation in bovine. The overexpression of in bovine primary skeletal muscle cells resulted in 483 differentially expressed genes (DEGs), including 224 upregulated DEGs and 259 downregulated DEGs. GO functional annotation analysis showed that muscle development-related biological processes such as muscle structure development and muscle cell proliferation were significantly enriched. KEGG pathway analysis revealed that the PI3K/AKT and MAPK signaling pathways were important pathways for DEG enrichment. Notably, we found that inhibited the mRNA and protein expression levels of the gene. Moreover, knockdown of the gene promoted the proliferation and apoptosis of bovine primary skeletal muscle cells. Finally, we showed that promoted the proliferation and apoptosis of bovine primary skeletal muscle cells by cis-modulation of in cattle. This work illustrates our discovery of the molecular mechanisms underlying the regulation of in the development of beef.
长链非编码RNA(lncRNAs)已被证明通过多种机制参与骨骼肌发育的调控。本研究揭示,(SRY盒转录因子6反义上游)是从牛性别决定区域Y(SRY)相关的高迁移率族盒6()基因上游反向转录而来。在不同发育阶段的咸安牛肌肉组织中显著差异表达。随后,敲低和过表达实验发现,促进了牛原代骨骼肌细胞的增殖、凋亡和分化。在牛原代骨骼肌细胞中过表达导致483个差异表达基因(DEGs),包括224个上调的DEGs和259个下调的DEGs。GO功能注释分析表明,肌肉结构发育和肌肉细胞增殖等与肌肉发育相关的生物学过程显著富集。KEGG通路分析显示,PI3K/AKT和MAPK信号通路是DEG富集的重要通路。值得注意的是,我们发现抑制了基因的mRNA和蛋白表达水平。此外,敲低基因促进了牛原代骨骼肌细胞的增殖和凋亡。最后,我们表明通过顺式调控牛中的促进了牛原代骨骼肌细胞的增殖和凋亡。这项工作阐述了我们对牛肉发育过程中调控分子机制的发现。