首页> 外文期刊>Mechanisms of Ageing and Development >mRNA levels of the linker histone variant, H1o, in mitotically active human diploid fibroblasts as a function of the phases of the cell cycle and cumulative population doublings.
【24h】

mRNA levels of the linker histone variant, H1o, in mitotically active human diploid fibroblasts as a function of the phases of the cell cycle and cumulative population doublings.

机译:有丝分裂活性的人类二倍体成纤维细胞中接头组蛋白变体H1o的mRNA水平是细胞周期和累积种群倍增的函数。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Senescence and differentiation have many similarities with respect to certain aspects of gene expression and cell cycle related events. One linker histone variant tightly associated with differentiation is the H1 variant, H1o. The work of this investigation has focused on the expression of H1o during the phases of the cell cycle and as a function of increasing cumulative population doublings (CPD) in an in vitro model ageing cell system, namely, human diploid fibroblasts. Increased H1o mRNA levels were found during the S phase of the cell cycle contrary to H1o protein relative synthesis rates, which were found to be increased during the Go phase of the cell cycle. These results were obtained in actively proliferating cell populations. However when the proliferative rate of the overall population begins to drop (CPD 50), H1o mRNA levels tend to remain stable throughout the Go, G1 and S phases. On the other hand, no changes in the H1o relative synthesis rates were found as a function of increasing CPD. Uncoupling of H1o protein and mRNA levels has been observed in numerous differentiating systems. The analogous mode in which H1o gene expression is regulated in both these two systems reinforces the opinion that senescence and differentiation may have similarities at the level of chromatin remodelling.
机译:关于基因表达和细胞周期相关事件的某些方面,衰老和分化具有许多相似性。与分化紧密相关的一个接头组蛋白变体是H1变体H1o。这项研究的工作集中在细胞周期各阶段的H10表达,以及在体外模型衰老细胞系统(即人类二倍体成纤维细胞)中增加累积种群倍增(CPD)的作用。在细胞周期的S阶段发现了H1o mRNA水平的增加,与H1o蛋白质的相对合成率相反,后者在细胞周期的Go阶段却相对增加。这些结果是在活跃增殖的细胞群体中获得的。但是,当总体人群的增生率开始下降(CPD 50)时,H10 mRNA水平在整个Go,G1和S期均趋于稳定。另一方面,没有发现H 10相对合成速率随CPD增加而变化。在许多区分系统中已经观察到H10蛋白和mRNA水平的解偶联。在这两个系统中都调节H1o基因表达的类似模式,强化了这样一种观点,即衰老和分化在染色质重塑水平上可能具有相似性。

著录项

相似文献

  • 外文文献
  • 中文文献
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