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The Wnt-target gene Dlk-1 is regulated by the Prmt5-associated factor Copr5 during adipogenic conversion

机译:Wnt靶基因Dlk-1在成脂转化过程中受Prmt5相关因子Copr5调控。

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Protein arginine methyl transferase 5 (Prmt5) regulates various differentiation processes, including adipogenesis. Here, we investigated adipogenic conversion in cells and mice in which Copr5 , a Prmt5- and histone-binding protein, was genetically invalidated. Compared to control littermates, the retroperitoneal white adipose tissue (WAT) of Copr5 KO mice was slightly but significantly reduced between 8 and 16 week/old and contained fewer and larger adipocytes. Moreover, the adipogenic conversion of Copr5 KO embryoid bodies (EB) and of primary embryo fibroblasts (Mefs) was markedly delayed. Differential transcriptomic analysis identified Copr5 as a negative regulator of the Dlk-1 gene, a Wnt target gene involved in the control of adipocyte progenitors cell fate. Dlk-1 expression was upregulated in Copr5 KO Mefs and the Vascular Stromal Fraction (VSF) of Copr5 KO WAT. Chromatin immunoprecipitation (ChIP) show that the ablation of Copr5 has impaired both the recruitment of Prmt5 and β-catenin at the Dlk-1 promoter. Overall, our data suggest that Copr5 is involved in the transcriptional control exerted by the Wnt pathway on early steps of adipogenesis.
机译:蛋白质精氨酸甲基转移酶5(Prmt5)调节各种分化过程,包括脂肪形成。在这里,我们研究了细胞和小鼠中的成脂转化,其中Copr5(一种Prmt5和组蛋白结合蛋白)在基因上是无效的。与对照组同窝仔相比,Copr5 KO小鼠的腹膜后白色脂肪组织(WAT)在8至16周/周龄之间略有减少,但明显减少,并且脂肪细胞越来越少。此外,Copr5 KO胚状体(EB)和原代成纤维细胞(Mefs)的成脂转化明显延迟。差异转录组学分析鉴定出Copr5是Dlk-1基因的负调控因子,Dlk-1基因是Wnt靶基因,参与控制脂肪细胞祖细胞的命运。 Dlk-1表达在Copr5 KO Mefs和Copr5 KO WAT的血管基质分数(VSF)中上调。染色质免疫沉淀(ChIP)表明,Copr5的消融损害了Dmt-1启动子上Prmt5和β-catenin的募集。总体而言,我们的数据表明Copr5参与了Wnt途径在脂肪形成的早期步骤中施加的转录控制。

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