首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >The Conserved Nad(h)-dependent Corepressor Ctbp-1 Regulates Caenorhabditis Elegans Life Span
【24h】

The Conserved Nad(h)-dependent Corepressor Ctbp-1 Regulates Caenorhabditis Elegans Life Span

机译:保守的依赖Nad(h)的Corepressor Ctbp-1调节秀丽隐杆线虫的寿命。

获取原文
获取原文并翻译 | 示例
       

摘要

CtBP (C-terminal binding protein) is an evolutionary conserved NAD(H)-dependent transcriptional corepressor, whose activity has been shown to be regulated by the NAD/NADH ratio. Although recent studies have provided significant new insights into mechanisms by which CtBP regulates transcription, the biological function of CtBP remains incompletely understood. Here, we report that genetic inactivation of the Caenorhabditis elegans homolog, ctbp-1, results in life span extension, which is suppressed by reintroduction of the ctbp-1 genomic DNA encoding wild-type but not NAD(H)-binding defective CTBP-1 protein. We show that CTBP-1 possibly modulates aging through the insulin/IGF-1 signaling pathway, dependent on the forkhead transcription factor DAF-16, but independent of the NAD-dependent histone deacety-Iase SIR-2.1. Genome-wide microarray analysis identifies > 200 potential CTBP-1 target genes. Importantly, RNAi inhibition of a putative triacylglycerol lipase gene lips-7(C09E8.2) but not another lipase suppresses the life span extension phenotype. Consistently, metabolic analysis shows that the triacylglycerol level is reduced in the ctbp-1 deletion mutant, which is restored to the wild-type level by RNAi inhibition of lips-7. Taken together, our data suggest that CTBP-1 controls life span probably through the regulation of lipid metabolism.
机译:CtBP(C末端结合蛋白)是一种进化保守的NAD(H)依赖性转录共表达因子,其活性已显示受NAD / NADH比的调节。尽管最近的研究为CtBP调节转录的机制提供了重要的新见解,但对CtBP的生物学功能仍未完全了解。在这里,我们报道了秀丽隐杆线虫同源物ctbp-1的基因失活导致寿命延长,这可以通过重新引入编码野生型而不是NAD(H)结合缺陷型CTBP-的ctbp-1基因组DNA来抑制。 1种蛋白质。我们显示CTBP-1可能通过胰岛素/ IGF-1信号通路调节衰老,这取决于叉头转录因子DAF-16,但独立于NAD依赖性组蛋白脱乙酰基酶SIR-2.1。全基因组微阵列分析可识别> 200个潜在的CTBP-1靶基因。重要的是,RNAi抑制推定的三酰基甘油脂肪酶基因lips-7(C09E8.2),而不抑制另一种脂肪酶抑制了寿命延长表型。一致地,代谢分析显示ctbp-1缺失突变体中的三酰基甘油水平降低,该突变体通过RNAi抑制Lips-7恢复到野生型水平。综上所述,我们的数据表明CTBP-1可能通过调节脂质代谢来控制寿命。

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