Multiple pathways for suppression of mutants affecting G1-specific tip transcription in Saccharomyces cerevisiae

被引:11
作者
Flick, K
Wittenberg, C
机构
[1] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
关键词
D O I
10.1534/genetics.104.032169
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In the budding yeast, Saccharomyces cerevisiae, control of cell proliferation is exerted primarily during G, phase. The G(1)-specific transcription of several hundred genes, many with roles in early cell cycle events, requires the transcription factors SBF and MBF, each composed of Swi6 and a DNA-binding protein, Swi4 or Mbp1, respectively. Binding of these factors to promoters is essential but insufficient for robust transcription. Timely transcriptional activation requires Cln3/CDK activity. To identify potential targets for Cln3/CDK, we identified multicopy suppressors of the temperature sensitivity of new conditional alleles of SW16. A bck2Delta background was used to render SUM essential. Seven multicopy suppressors of bck2Delta swi6-ts mutants were identified. Three genes, SW14, RME1, and CLN2, were identified previously in related screens and shown to activate G(1)-specific expression of genes independent of CLN3 and SW16. The other four genes, FBA1, RPL40a/UBII, GIN4, and PAB1, act via apparently unrelated pathways downstream of SBF and MBF. Each depends upon CLN2, but not CLN1, for its suppressing activity. Together with additional characterization these findings indicate that multiple independent pathways are sufficient for proliferation in the absence of G(1)-specific transcriptional activators.
引用
收藏
页码:37 / 49
页数:13
相关论文
共 67 条
[1]   MUTATIONAL ANALYSIS OF A DNA-SEQUENCE INVOLVED IN LINKING GENE-EXPRESSION TO THE CELL-CYCLE [J].
ANDREWS, BJ ;
MOORE, L .
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 1992, 70 (10-11) :1073-1080
[2]   Nim1-related kinases coordinate cell cycle progression with the organization of the peripheral cytoskeleton in yeast [J].
Barral, Y ;
Parra, M ;
Bidlingmaier, S ;
Snyder, M .
GENES & DEVELOPMENT, 1999, 13 (02) :176-187
[3]   Cla4p, a Saccharomyces cerevisiae Cdc42p-activated kinase involved in cytokinesis, is activated at mitosis [J].
Benton, BK ;
Tinkelenberg, A ;
Gonzalez, I ;
Cross, FR .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (09) :5067-5076
[4]   The Swi5 activator recruits the Mediator complex to the HO promoter without RNA polymerase II [J].
Bhoite, LT ;
Yu, YX ;
Stillman, DJ .
GENES & DEVELOPMENT, 2001, 15 (18) :2457-2469
[5]   PROPERTIES OF SACCHAROMYCES-CEREVISIAE WEE1 AND ITS DIFFERENTIAL REGULATION OF P34(CDC28) IN RESPONSE TO G(1) AND G(2) CYCLINS [J].
BOOHER, RN ;
DESHAIES, RJ ;
KIRSCHNER, MW .
EMBO JOURNAL, 1993, 12 (09) :3417-3426
[6]  
Breeden L, 1996, CURR TOP MICROBIOL, V208, P95
[7]   2 DIFFERENTIALLY REGULATED MESSENGER-RNAS WITH DIFFERENT 5' ENDS ENCODE SECRETED AND INTRACELLULAR FORMS OF YEAST INVERTASE [J].
CARLSON, M ;
BOTSTEIN, D .
CELL, 1982, 28 (01) :145-154
[8]   The role of Cdc42p GTPase-activating proteins in assembly of the septin ring in yeast [J].
Caviston, JP ;
Longtine, M ;
Pringle, JR ;
Bi, E .
MOLECULAR BIOLOGY OF THE CELL, 2003, 14 (10) :4051-4066
[9]  
CHEN YR, 1995, MOL CELL BIOL, V15, P4631
[10]   Yeast Eap1p, an elF4E-associated protein, has a separate function involving genetic stability [J].
Chial, HJ ;
Stemm-Wolf, AJ ;
McBratney, S ;
Winey, M .
CURRENT BIOLOGY, 2000, 10 (23) :1519-1522