ACE2 is required for daughter cell-specific G1 delay in Saccharomyces cerevisiae

被引:61
作者
Laabs, TL
Markwardt, DD
Slattery, MG
Newcomb, LL
Stillman, DJ
Heideman, W
机构
[1] Univ Wisconsin, Sch Pharm, Madison, WI 53705 USA
[2] Univ Wisconsin, Dept Biomol Chem, Madison, WI 53705 USA
[3] Univ Utah, Dept Pathol, Salt Lake City, UT 84112 USA
关键词
D O I
10.1073/pnas.1833999100
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
Saccharomyces cerevisiae cells reproduce by budding to yield a mother cell and a smaller daughter cell. Although both mother and daughter begin G(1) simultaneously, the mother cell progresses through G(1) more rapidly. Daughter cell G(1) delay has long been thought to be due to a requirement for attaining a certain critical cell size before passing the commitment point in the cell cycle known as START. We present an alternative model in which the daughter cell-specific Ace2 transcription factor delays G(1) in daughter cells. Deletion of ACE2 produces daughter cells that proceed through G(1) at the same rate as mother cells, whereas a mutant Ace2 protein that is not restricted to daughter cells delays G(1) equally in both mothers and daughters. The differential in G(1) length between mothers and daughters requires the Cln3 G(1)cyclin, and CLN3-GFP reporter expression is reduced in daughters in an ACE2-dependent manner. Specific daughter delay elements in the CLN3 promoter are required for normal daughter G(1) delay, and these elements bind to an unidentified 127-kDa protein. This DNA-binding activity is enhanced by deletion of ACE2. These results support a model in which daughter cell G(1) delay is determined not by cell size but by an intrinsic property of the daughter cell generated by asymmetric cell division.
引用
收藏
页码:10275 / 10280
页数:6
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