...
首页> 外文期刊>Oncogene >Hypoxic regulation of stability of connective tissue growth factor|[sol]|CCN2 mRNA by 3|[prime]|-untranslated region interacting with a cellular protein in human chondrosarcoma cells
【24h】

Hypoxic regulation of stability of connective tissue growth factor|[sol]|CCN2 mRNA by 3|[prime]|-untranslated region interacting with a cellular protein in human chondrosarcoma cells

机译:缺氧调节结缔组织生长因子| [sol] | CCN2 mRNA与人软骨肉瘤细胞中3 | [prime] |-非翻译区与细胞蛋白相互作用的稳定性

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Connective tissue growth factor (CTGF/CCN2) can be induced by various forms of stress such as exposure to high glucose, mechanical load, or hypoxia. Here, we investigated the molecular mechanism involved in the induction of ctgf/ccn2 by hypoxia in a human chondrosarcoma cell line, HCS-2/8. Hypoxia increased the ctgf/ccn2 mRNA level by altering the 3'-untranslated region (UTR)-mediated mRNA stability without requiring de novo protein synthesis. After a series of extensive analyses, we eventually found that the cis-repressive element of 84 bases within the 3'-UTR specifically bound to a cytoplasmicuclear protein. By conducting a UV crosslinking assay, we found the cytoplasmicuclear protein to be a 35kDa molecule that bound to the cis-element in a hypoxia-inducible manner. These results suggest that a cis-element in the 3'-UTR of ctgf/ccn2 mRNA and trans-factor counterpart(s) play an important role in the post-transcriptional regulation by determining the stability of ctgf/ccn2 mRNA.
机译:结缔组织生长因子(CTGF / CCN2)可以通过各种形式的压力来诱导,例如暴露于高葡萄糖,机械负荷或缺氧状态。在这里,我们研究了在人软骨肉瘤细胞系HCS-2 / 8中低氧诱导ctgf / ccn2的分子机制。缺氧通过改变3'-非翻译区(UTR)介导的mRNA稳定性而无需重新合成蛋白质,从而提高了ctgf / ccn2 mRNA水平。经过一系列广泛的分析,我们最终发现3'-UTR内84个碱基的顺式阻遏元件与细胞质/核蛋白特异性结合。通过进行紫外线交联测定,我们发现细胞质/核蛋白是一个35kDa分子,以低氧诱导的方式与顺式元件结合。这些结果表明,通过确定ctgf / ccn2 mRNA的稳定性,ctgf / ccn2 mRNA 3'-UTR中的顺式元件和反式对应物在转录后调控中起着重要作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号