Department of Pharmaceutical Sciences, Washington State University College of Pharmacy, PO Box 1495, Spokane, WA 99210, USA.
Genes (Basel). 2016 Jun 28;7(7):30. doi: 10.3390/genes7070030.
Telomerase, regulated primarily by the transcription of its catalytic subunit telomerase reverse transcriptase (TERT), is critical for controlling cell proliferation and tissue homeostasis by maintaining telomere length. Although there is a high conservation between human and mouse TERT genes, the regulation of their transcription is significantly different in these two species. Whereas mTERT expression is widely detected in adult mice, hTERT is expressed at extremely low levels in most adult human tissues and cells. As a result, mice do not exhibit telomere-mediated replicative aging, but telomere shortening is a critical factor of human aging and its stabilization is essential for cancer development in humans. The chromatin environment and epigenetic modifications of the hTERT locus, the binding of transcriptional factors to its promoter, and recruitment of nucleosome modifying complexes all play essential roles in restricting its transcription in different cell types. In this review, we will discuss recent progress in understanding the molecular mechanisms of TERT regulation in human and mouse tissues and cells, and during cancer development.
端粒酶主要通过其催化亚基端粒酶逆转录酶(TERT)的转录来调控,通过维持端粒长度,对控制细胞增殖和组织稳态至关重要。尽管人类和小鼠的 TERT 基因高度保守,但在这两个物种中,其转录的调控有显著差异。尽管 mTERT 在成年小鼠中广泛表达,但 hTERT 在大多数成年人类组织和细胞中表达水平极低。因此,小鼠不会表现出端粒介导的复制性衰老,但端粒缩短是人类衰老的关键因素,其稳定对人类癌症的发展至关重要。hTERT 基因座的染色质环境和表观遗传修饰、转录因子与其启动子的结合以及核小体修饰复合物的募集,在不同细胞类型中端粒酶转录的限制中都发挥着重要作用。在这篇综述中,我们将讨论在人类和小鼠组织和细胞以及癌症发展过程中,TERT 调控的分子机制的最新进展。