端粒酶
端粒
核糖核酸
生物
赫拉
体细胞
端粒酶RNA组分
分子生物学
端粒酶逆转录酶
DNA
生殖系
转染
感应(电子)
细胞培养
基因
遗传学
化学
物理化学
作者
Junli Feng,Walter D. Funk,Sy-Shi Wang,Scott L. Weinrich,Ariel A. Avilion,Choy‐Pik Chiu,Robert R. Adams,Edwin Chang,Richard Allsopp,Jinghua Yu,Siyuan Le,Michael D. West,Calvin B. Harley,William H. Andrews,Carol W. Greider,Bryant Villeponteau
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1995-09-01
卷期号:269 (5228): 1236-1241
被引量:2245
标识
DOI:10.1126/science.7544491
摘要
Eukaryotic chromosomes are capped with repetitive telomere sequences that protect the ends from damage and rearrangements. Telomere repeats are synthesized by telomerase, a ribonucleic acid (RNA)-protein complex. Here, the cloning of the RNA component of human telomerase, termed hTR, is described. The template region of hTR encompasses 11 nucleotides (5′-CUAACCCUAAC) complementary to the human telomere sequence (TTAGGG) n . Germline tissues and tumor cell lines expressed more hTR than normal somatic cells and tissues, which have no detectable telomerase activity. Human cell lines that expressed hTR mutated in the template region generated the predicted mutant telomerase activity. HeLa cells transfected with an antisense hTR lost telomeric DNA and began to die after 23 to 26 doublings. Thus, human telomerase is a critical enzyme for the long-term proliferation of immortal tumor cells.
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