Wang Yilin, Wang Yan, Zhong Tao, Guo Jiazhong, Li Li, Zhang Hongping, Wang Linjie
Institute of Animal Genetics and Breeding, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, Sichuan, People's Republic of China.
Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu, Sichuan, People's Republic of China.
Mol Cell Biochem. 2017 Jan;424(1-2):203-208. doi: 10.1007/s11010-016-2856-1. Epub 2016 Oct 26.
Glycogen synthase kinase 3β (GSK3β) is a ubiquitous serine/threonine kinase and has important roles in glycogen metabolism biosynthesis. Studies have revealed that GSK3β can directly regulate the glycogen synthase activity, yet little is known about the regulation of GSK3β on GYS1 gene transcription. Here, we show that overexpression of GSK3β decreased the mRNA expression level of GYS1. Then we cloned approximately 1.5 kb of pig GYS1 gene promoter region, generated sequential deletion constructs, and evaluated their activity. A gradual increase of the promoter activity was seen with increasing length of the promoter sequence, reaching its highest activity to the sequence corresponding to nt -350 to +224, and then decreased. However, the activities of constructed promoter fragments show different responses to GSK3β co-transfection. By analyzing a series of GYS1 promoter reporter constructs, we have defined two crucial regions (-1488 to -539, -350 to -147) that are responsible for GSK3β-induced transcriptional repression. Furthermore, the ChIP results revealed that only the first and second NF-κB sites of GYS1 promoter could bind to p65, and overexpression of GSK3β induced a significant decrease in p65 binding to the second NF-κB binding site, suggesting that GSK3β may regulate expression of GYS1 gene through binding to the second rather than the first NF-κB site. These data suggest that the NF-κB plays important roles in the transcriptional activity of pig GYS1 gene regulated by GSK3β.
糖原合酶激酶3β(GSK3β)是一种普遍存在的丝氨酸/苏氨酸激酶,在糖原代谢生物合成中发挥重要作用。研究表明,GSK3β可直接调节糖原合酶活性,但关于GSK3β对GYS1基因转录的调控知之甚少。在此,我们发现GSK3β的过表达降低了GYS1的mRNA表达水平。随后,我们克隆了约1.5 kb的猪GYS1基因启动子区域,构建了一系列缺失片段,并评估了它们的活性。随着启动子序列长度的增加,启动子活性逐渐升高,在对应于nt -350至+224的序列处达到最高活性,随后下降。然而,构建的启动子片段活性对GSK3β共转染表现出不同的反应。通过分析一系列GYS1启动子报告基因构建体,我们确定了两个关键区域(-1488至-539,-350至-147),它们负责GSK3β诱导的转录抑制。此外,染色质免疫沉淀结果显示,只有GYS1启动子的第一个和第二个NF-κB位点能与p65结合,且GSK3β的过表达导致p65与第二个NF-κB结合位点的结合显著减少,这表明GSK3β可能通过与第二个而非第一个NF-κB位点结合来调节GYS1基因的表达。这些数据表明,NF-κB在GSK3β调控的猪GYS1基因转录活性中起重要作用。