Quyangangmao Su, Zhanhong Gao, Fengshuo Zhang, Zhenling Wu, Qiurong Ji, Kaina Zhu, Linsheng Gui
{"title":"Effect of miR-10a on the proliferation and differentiation of yak adipocyte precursors.","authors":"Quyangangmao Su, Zhanhong Gao, Fengshuo Zhang, Zhenling Wu, Qiurong Ji, Kaina Zhu, Linsheng Gui","doi":"10.1007/s13353-024-00932-6","DOIUrl":null,"url":null,"abstract":"<p><p>The fat content of yak meat is significantly correlated with the meat quality, and an appropriate fat content helps to improve the texture of the meat. The involvement of miR-10a in regulating the differentiation and proliferation of various cell types has been reported. Therefore, in this study, the effects of miR-10a on lipid droplet accumulation were investigated by transfection of yak adipocyte precursors with an miR-10a inhibitor, followed by Oil Red O, BODIPY, EdU staining, and cell cycle analysis of the transfected and control cells. The relative expression of lipogenic marker genes was determined by RT-qPCR to clarify the effect of miR-10a on the differentiation and proliferation of yak adipocyte precursors. Mature adipocytes were collected for transcriptome analysis to identify differentially expressed target genes and the association of these genes with adipogenic pathways was investigated by GO and KEGG enrichment analyses. In addition, the phylogeny and expression profiles of miR-10a were analyzed in various yak tissues. The results showed that miR-10a could inhibit the differentiation and promote the proliferation of yak adipocyte precursors. Analysis of the RNA-Seq results showed that miR-10a inhibitor and inhibitor NC had six differentially expressed genes: FABP4, AKR1B7, IGF2, ROCK1, IFNB1, and PLA2G3. These genes were found to be involved in the regulation of adipogenesis, with IGF2 and IFNB1 being upregulated in the PI3K-Akt signaling pathway, which is activated upon stimulation by IGF2 and IFNB1 and inhibits the differentiation and promotes the proliferation of yak adipocytes precursor, which in turn affected adipogenesis. Moreover, phylogenetic analysis indicated that miR-10a evolved relatively recently in yak and sheep, while tissue expression profiles showed that miR-10a was highly expressed in yak lung tissues.</p>","PeriodicalId":14891,"journal":{"name":"Journal of Applied Genetics","volume":" ","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2024-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Applied Genetics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s13353-024-00932-6","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The fat content of yak meat is significantly correlated with the meat quality, and an appropriate fat content helps to improve the texture of the meat. The involvement of miR-10a in regulating the differentiation and proliferation of various cell types has been reported. Therefore, in this study, the effects of miR-10a on lipid droplet accumulation were investigated by transfection of yak adipocyte precursors with an miR-10a inhibitor, followed by Oil Red O, BODIPY, EdU staining, and cell cycle analysis of the transfected and control cells. The relative expression of lipogenic marker genes was determined by RT-qPCR to clarify the effect of miR-10a on the differentiation and proliferation of yak adipocyte precursors. Mature adipocytes were collected for transcriptome analysis to identify differentially expressed target genes and the association of these genes with adipogenic pathways was investigated by GO and KEGG enrichment analyses. In addition, the phylogeny and expression profiles of miR-10a were analyzed in various yak tissues. The results showed that miR-10a could inhibit the differentiation and promote the proliferation of yak adipocyte precursors. Analysis of the RNA-Seq results showed that miR-10a inhibitor and inhibitor NC had six differentially expressed genes: FABP4, AKR1B7, IGF2, ROCK1, IFNB1, and PLA2G3. These genes were found to be involved in the regulation of adipogenesis, with IGF2 and IFNB1 being upregulated in the PI3K-Akt signaling pathway, which is activated upon stimulation by IGF2 and IFNB1 and inhibits the differentiation and promotes the proliferation of yak adipocytes precursor, which in turn affected adipogenesis. Moreover, phylogenetic analysis indicated that miR-10a evolved relatively recently in yak and sheep, while tissue expression profiles showed that miR-10a was highly expressed in yak lung tissues.
牦牛肉的脂肪含量与肉质呈显著相关,适宜的脂肪含量有助于改善肉质的质地。miR-10a参与调节多种细胞类型的分化和增殖已有报道。因此,本研究通过miR-10a抑制剂转染牦牛脂肪细胞前体,然后对转染细胞和对照细胞进行Oil Red O、BODIPY、EdU染色,并对转染细胞和对照细胞进行细胞周期分析,研究miR-10a对脂滴积累的影响。通过RT-qPCR检测脂肪生成标记基因的相对表达,阐明miR-10a对牦牛脂肪细胞前体分化和增殖的影响。收集成熟脂肪细胞进行转录组分析,以鉴定差异表达的靶基因,并通过GO和KEGG富集分析研究这些基因与脂肪形成途径的关联。此外,我们还分析了miR-10a在牦牛不同组织中的系统发育和表达谱。结果表明,miR-10a能够抑制牦牛脂肪细胞前体的分化,促进其增殖。RNA-Seq结果分析显示,miR-10a抑制剂和抑制剂NC有6个差异表达基因:FABP4、AKR1B7、IGF2、ROCK1、IFNB1和PLA2G3。这些基因被发现参与脂肪形成的调控,其中IGF2和IFNB1在PI3K-Akt信号通路中被上调,在IGF2和IFNB1的刺激下,PI3K-Akt信号通路被激活,抑制牦牛脂肪细胞前体的分化并促进其增殖,进而影响脂肪形成。此外,系统发育分析表明,miR-10a在牦牛和绵羊中进化较晚,而组织表达谱显示,miR-10a在牦牛肺组织中高表达。
期刊介绍:
The Journal of Applied Genetics is an international journal on genetics and genomics. It publishes peer-reviewed original papers, short communications (including case reports) and review articles focused on the research of applicative aspects of plant, human, animal and microbial genetics and genomics.