Human Flap Endonuclease I Is in Complex with Telomerase and Is Required for Telomerase-mediated Telomere Maintenance

被引:29
|
作者
Sampathi, Shilpa [1 ,2 ]
Bhusari, Amruta [3 ]
Shen, Binghui [4 ,5 ]
Chai, Weihang [1 ,2 ]
机构
[1] Washington State Univ, WWAMI Med Educ Program, Spokane, WA 99210 USA
[2] Washington State Univ, Sch Mol Biosci, Spokane, WA 99210 USA
[3] Texas Womans Univ, Dept Biol, Denton, TX 76204 USA
[4] City Hope Natl Med Ctr, Dept Radiat Biol, Duarte, CA 91010 USA
[5] Beckman Res Inst, Duarte, CA 91010 USA
基金
美国国家卫生研究院;
关键词
DNA-DAMAGE RESPONSE; HOMOLOGOUS RECOMBINATION; SACCHAROMYCES-CEREVISIAE; CELLULAR SENESCENCE; CATALYTIC SUBUNIT; HUMAN-CHROMOSOMES; POLYMERASE ALPHA; END REPLICATION; STEM-CELLS; LENGTH;
D O I
10.1074/jbc.M805362200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Studies from budding yeast and ciliates have suggested that telomerase extension of telomeres requires the conventional DNA replication machinery, yet little is known about how DNA replication proteins regulate telomerase action in higher eukaryotic cells. Here we investigate the role of one of the DNA replication factors, flap endonuclease I (FEN1), in regulating telomerase activity in mammalian cells. FEN1 is a nuclease that plays an important role in DNA replication, repair, and recombination. We show that FEN1 is in complex with telomerase in vivo via telomeric DNA. We further demonstrate that FEN1 deficiency in mouse embryonic fibroblasts leads to an increase in telomere end-to-end fusions. In cancer cells, FEN1 deficiency induces gradual shortening of telomeres but does not alter the single-stranded G-overhangs. This is, to our knowledge, the first evidence that FEN1 and telomerase physically co-exist as a complex and that FEN1 can regulate telomerase activity at telomeres in mammalian cells.
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页码:3682 / 3690
页数:9
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