Dynamics of DNA double-strand breaks revealed by clustering of damaged chromosome domains

被引:399
作者
Aten, JA
Stap, J
Krawczyk, PM
van Oven, CH
Hoebe, RA
Essers, J
Kanaar, R
机构
[1] Erasmus MC Daniel den Hoed, Erasmus Med Ctr, Dept Cell Biol & Genet, NL-3000 DR Rotterdam, Netherlands
[2] Erasmus MC Daniel den Hoed, Dept Radiat Oncol, NL-3000 DR Rotterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Dept Cell Biol & Histol, Ctr Microscopial Res, NL-1100 DE Amsterdam, Netherlands
关键词
D O I
10.1126/science.1088845
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Interactions between ends from different DNA double-strand breaks (DSBs) can produce tumorigenic chromosome translocations. Two theories for the juxtaposition of DSBs in translocations, the static "contact-first" and the dynamic "breakage-first" theory, differ fundamentally in their requirement for DSB mobility. To determine whether or not DSB-containing chromosome domains are mobile and can interact, we introduced linear tracks of DSBs in nuclei. We observed changes in track morphology within minutes after DSB induction, indicating movement of the domains. In a subpopulation of cells, the domains clustered. Juxtaposition of different DSB-containing chromosome domains through clustering, which was most extensive in G1 phase cells, suggests an adhesion process in which we implicate the Mre11 complex. Our results support the breakage-first theory to explain the origin of chromosomal translocations.
引用
收藏
页码:92 / 95
页数:4
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