Human heterochromatin protein 1 isoforms HP1Hsα and HP1Hsβ interfere with hTERT-telomere interactions and correlate with changes in cell growth and response to ionizing radiation

被引:74
作者
Sharma, GG
Hwang, KK
Pandita, RK
Gupta, A
Dhar, S
Parenteau, J
Agarwal, M
Worman, HJ
Wellinger, RJ
Pandita, TK
机构
[1] Washington Univ, Sch Med, Radiat & Canc Biol Div, St Louis, MO 63108 USA
[2] Columbia Univ, Coll Phys & Surg, New York, NY 10032 USA
[3] Univ Sherbrooke, Sherbrooke, PQ J1H 5N4, Canada
[4] Yeshiva Univ Albert Einstein Coll Med, Bronx, NY 10461 USA
关键词
D O I
10.1128/MCB.23.22.8363-8376.2003
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
Telomeres are associated with the nuclear matrix and are thought to be heterochromatic. We show here that in human cells the overexpression of green fluorescent protein-tagged heterochromatin protein 1 (GFP-HP1) or nontagged HP1 isoforms HP1(Hsalpha) or HP1(Hsbeta), but not HP1(Hsgamma), results in decreased association of a catalytic unit of telomerase (hTERT) with telomeres. However, reduction of the G overhangs and overall telomere sizes was found in cells overexpressing any of these three proteins. Cells overexpressing HP1(Hsalpha) or HP1(Hsbeta) also display a higher frequency of chromosome end-to-end associations and spontaneous chromosomal damage than the parental cells. None of these effects were observed in cells expressing mutants of GFP-DeltaHP1(Hsalpha), GFP-DeltaHP1(Hsbeta), or GFP-DeltaHP1(Hsgamma) that had their chromodomains deleted. An increase in the cell population doubling time and higher sensitivity to cell killing by ionizing radiation (IR) treatment was also observed for cells overexpressing HP1(Hsalpha) or HP1(Hsbeta). In contrast, cells expressing mutant GFP-DeltaHP1(Hsalpha) or GFP-DeltaHP1(Hsbeta) showed a decrease in population doubling time and decreased sensitivity to IR compared to the parental cells. The effects on cell doubling times were paralleled by effects on tumorigenicity in mice: overexpression of HP1(HSalpha) or HP1(Hsbeta) suppressed tumorigenicity, whereas expression of mutant HP1(Hsalpha) or HP1(Hsbeta) did not. Collectively, the results show that human cells are exquisitely sensitive to the amount of HP1(Hsalpha) or HP1(Hsbeta) present, as their overexpression influences telomere stability, population doubling time, radioresistance, and tumorigenicity in a mouse xenograft model. In addition, the isoform-specific effects on telomeres reinforce the notion that telomeres are in a heterochromatinized state.
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页码:8363 / 8376
页数:14
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