CLB5-dependent activation of late replication origins in S-cerevisiae

被引:161
作者
Donaldson, AD
Raghuraman, MK
Friedman, KL
Cross, FR
Brewer, BJ
Fangman, WL
机构
[1] Univ Washington, Dept Genet, Seattle, WA 98195 USA
[2] Rockefeller Univ, New York, NY 10021 USA
关键词
D O I
10.1016/S1097-2765(00)80127-6
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
Replication origins in chromosomes are activated at specific times during the S phase. We show that the B-type cyclins are required for proper execution of this temporal program. clb5 cells activate early origins but not late origins, explaining the previously described long clb5 S phase. Origin firing appears normal in clb6 mutants. In clb5 clb6 double mutant cells, the late origin firing defect is suppressed, accounting for the normal duration of the phase despite its delayed onset. Therefore, Clb5p promotes the timely activation of early and late origins, but Clb6p can activate only early origins. In clb5 clb6 mutants, the other B-type cyclins (Clb1-4p) promote an S phase during which both early and late replication origins fire.
引用
收藏
页码:173 / 182
页数:10
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