Wang Chongyang, Luo Cheng, Zhang Hao, Li Xin, Li Yanyan, Xiong Yan, Wang Youli, Lin Yaqiu
College of Animal & Veterinary Sciences, Southwest Minzu University, Chengdu 610041, Sichuan, China.
Key Laboratory of Qinghai-Tibetan Plateau Animal Genetic Resource Protection and Utilization, Ministry of Education/Sichuan Province, Southwest Minzu University, Chengdu 610041, Sichuan, China.
Sheng Wu Gong Cheng Xue Bao. 2022 Aug 25;38(8):2939-2947. doi: 10.13345/j.cjb.220299.
The aim of this study was to investigate the effect of activating transcription factor 3 (3) on the differentiation of intramuscular preadipocytes in goat, and to elucidate its possible action pathway at the molecular level. In this study, the recombinant plasmid of goat pEGFP-N1-3 was constructed, and the intramuscular preadipocytes were transfected with liposomes. The relative expression levels of adipocyte differentiation marker genes were detected by quantitative real-time PCR (qRT-PCR). After transfection of goat intramuscular preadipocytes with the goat pEGFP-N1-3 overexpression vector, it was found that the accumulation of lipid droplets was inhibited, and the adipocyte differentiation markers , / and 1 were extremely significantly down-regulated ( < 0.01), while / and 2 were significantly down-regulated ( < 0.05). The 3 binding sites were predicted to exist in the promoter regions of , / and 2 by the ALGGEN PROMO program. The overexpression of goat 3 inhibits the accumulation of lipid droplets in intramuscular preadipocytes, and this effect may be achieved by down-regulating , / and 2. These results may facilitate elucidation of the regulatory mechanism of 3 in regulating the differentiation of goat intramuscular preadipocytes.
本研究旨在探讨激活转录因子3(ATF3)对山羊肌内前体脂肪细胞分化的影响,并在分子水平阐明其可能的作用途径。本研究构建了山羊pEGFP-N1-ATF3重组质粒,并用脂质体转染肌内前体脂肪细胞。通过实时荧光定量PCR(qRT-PCR)检测脂肪细胞分化标志基因的相对表达水平。用山羊pEGFP-N1-ATF3过表达载体转染山羊肌内前体脂肪细胞后,发现脂滴积累受到抑制,脂肪细胞分化标志物PPARγ、C/EBPα和FABP4极显著下调(P<0.01),而LPL和aP2显著下调(P<0.05)。通过ALGGEN PROMO程序预测PPARγ、C/EBPα和LPL的启动子区域存在ATF3结合位点。山羊ATF3过表达抑制肌内前体脂肪细胞中脂滴的积累,这种作用可能是通过下调PPARγ、C/EBPα和LPL来实现的。这些结果可能有助于阐明ATF3调控山羊肌内前体脂肪细胞分化的调控机制。