Ouellette M M, Aisner D L, Savre-Train I, Wright W E, Shay J W
Department of Cell Biology and Neuroscience, The University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas, 75235-9039, USA.
Biochem Biophys Res Commun. 1999 Jan 27;254(3):795-803. doi: 10.1006/bbrc.1998.0114.
The forced expression of the catalytic subunit of human telomerase, hTERT, produces telomerase activity, allows telomere maintenance, and extends the cellular life span of IMR90 human lung fibroblasts. The mutation D869A abolishes both the catalytic activity of hTERT and its ability to extend cellular life span, demonstrating that the immortalizing capabilities of the enzyme are dependent on active catalysis. A second mutant of hTERT was examined that contains three copies of an HA epitope inserted at the C-terminus. This mutant produced telomerase activity in fibroblasts that was virtually indistinguishable from that of wild type telomerase when assayed in vitro. However, the forced expression of this mutant failed to maintain telomeres or extend cellular life span. Our results show that the catalytic activity of hTERT is required for cellular immortalization but that the presence of active telomerase does not necessarily imply telomere maintenance and immortality.
人端粒酶催化亚基hTERT的强制表达可产生端粒酶活性,维持端粒,并延长IMR90人肺成纤维细胞的细胞寿命。D869A突变消除了hTERT的催化活性及其延长细胞寿命的能力,表明该酶的永生化能力依赖于活性催化。研究了hTERT的第二个突变体,该突变体在C端插入了三个HA表位拷贝。当在体外检测时,该突变体在成纤维细胞中产生的端粒酶活性与野生型端粒酶几乎没有区别。然而,该突变体的强制表达未能维持端粒或延长细胞寿命。我们的结果表明,hTERT的催化活性是细胞永生化所必需的,但活性端粒酶的存在并不一定意味着端粒维持和永生化。