TRANSCRIPTIONAL ACTIVATION OF CLN1, CLN2, AND A PUTATIVE NEW G1-CYCLIN (HCS26) BY SWI4, A POSITIVE REGULATOR OF G1-SPECIFIC TRANSCRIPTION

被引:277
作者
OGAS, J
ANDREWS, BJ
HERSKOWITZ, I
机构
[1] UNIV CALIF SAN FRANCISCO, DEPT BIOCHEM & BIOPHYS, PROGRAM GENET, SAN FRANCISCO, CA 94143 USA
[2] UNIV TORONTO, DEPT MED & MOLEC GENET, TORONTO M5S 1A8, ONTARIO, CANADA
关键词
D O I
10.1016/0092-8674(91)90445-5
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
SWI4 of budding yeast codes for a component of a transcription factor (cell cycle box factor, or CCBF) necessary for G1-specific expression of HO. We show that SWI4 is essential for haploid cell viability at high temperature and in a/alpha-cells at all temperatures: SWI4-deficient cells arrest as large unbudded cells. Eight high copy number plasmids were identified that allow swi4- strains to grow under nonpermissive conditions. Two carry G1 cyclin genes, CLN1 and CLN2; another carries HCS26, coding for a putative cyclin. a/alpha-swi4- mutants exhibit 3- to 20-fold reductions in the levels of CLN1, CLN2, and HCS26 transcripts. The requirement of SWI4 for transcription appears to be direct: each gene contains sites similar to the CCBF-binding site; CCBF binds to the upstream region of HCS26. We propose that SWI4 participates in a positive feedback loop by which CLN1, CLN2, and possibly HCS26 promote their own transcription in G1.
引用
收藏
页码:1015 / 1026
页数:12
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