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小鼠Gas6启动子的鉴定与表征

Identification and characterization of mouse Gas6 promoter.

作者信息

Wang Jiayi, Qiao Yongxia, Sun Fenyong, Wan Yang, Huang Ting, Ye Tingjun, Yu Yongchun

机构信息

Department of Laboratory Centre, Shanghai 10th People's Hospital of Tongji University, Shanghai 200072, PR China.

出版信息

Biochem Biophys Res Commun. 2008 Jul 4;371(3):567-72. doi: 10.1016/j.bbrc.2008.04.130. Epub 2008 May 5.

Abstract

In this study, we identify and characterize the promoter of the mouse Gas6 gene, a negative regulator of chondrogenic differentiation. We identified two highly conserved regions within the core Gas6 promoter, which are conserved among mouse, human, and rat Gas6 genes, named A-BOX and B-BOX. Basal transcriptional activity was significantly reduced after deletion of either the A-BOX or the latter half of the B-BOX. After treatment with BMP-2 for 3 days, putative A-BOX Binding Factor(s) B (ABFB) and B-BOX Binding Factor(s) (BBF) were unable to bind to their specific motifs in C3H10T1/2 cells, compared with untreated control cells. In addition, we confirmed binding of an NF-Y site within the core promoter region of mouse Gas6 gene. Taken together, these observations provide insight into the mechanism by which Gas6 is downregulated during mesenchymal stem cells differentiation into chondrocytes.

摘要

在本研究中,我们鉴定并表征了小鼠Gas6基因的启动子,该基因是软骨形成分化的负调节因子。我们在Gas6核心启动子内鉴定出两个高度保守的区域,它们在小鼠、人类和大鼠的Gas6基因中保守,分别命名为A盒和B盒。缺失A盒或B盒后半部分后,基础转录活性显著降低。与未处理的对照细胞相比,用BMP-2处理3天后,推定的A盒结合因子B(ABFB)和B盒结合因子(BBF)在C3H10T1/2细胞中无法与其特定基序结合。此外,我们证实了小鼠Gas6基因核心启动子区域内NF-Y位点的结合。综上所述,这些观察结果为间充质干细胞向软骨细胞分化过程中Gas6下调的机制提供了见解。

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