Ume1p represses meiotic gene transcription in Saccharomyces cerevisiae through interaction with the histone deacetylase Rpd3p

被引:22
作者
Mallory, MJ [1 ]
Strich, R [1 ]
机构
[1] Fox Chase Canc Ctr, Inst Canc Res, Philadelphia, PA 19111 USA
关键词
D O I
10.1074/jbc.M308632200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Ume1p is a member of a conserved protein family including RbAp48 that associates with histone deacetylases. Consistent with this finding, Ume1p is required for the full repression of a subset of meiotic genes during vegetative growth in budding yeast. In addition to mitotic cell division, this report describes a new role for Ume1p in meiotic gene repression in precommitment sporulating cultures returning to vegetative growth. However, Ume1p is not required to re-establish repression as part of the meiotic transient transcription program. Mutational analysis revealed that two conserved domains (NEE box and a WD repeat motif) are required for Ume1p-dependent repression. Co-immunoprecipitation studies revealed that both the NEE box and the WD repeat motif are essential for normal Rpd3p binding. Finally, Ume1p-Rpd3p association is dependent on the global co-repressor Sin3p. Moreover, this activity was localized to one of the four paired amphipathic-helix domains of Sin3p shown previously to be required for transcriptional repression. These findings support a model that Ume1p binding to Rpd3p is required for its repression activity. In addition, these results suggest that Rpd3-Ume1p-Sin3p comprises an interdependent complex required for mediating transcriptional repression.
引用
收藏
页码:44727 / 44734
页数:8
相关论文
共 56 条
[1]
THE SAD1/RAD53 PROTEIN-KINASE CONTROLS MULTIPLE CHECKPOINTS AND DNA DAMAGE-INDUCED TRANSCRIPTION IN YEAST [J].
ALLEN, JB ;
ZHOU, Z ;
SIEDE, W ;
FRIEDBERG, EC ;
ELLEDGE, SJ .
GENES & DEVELOPMENT, 1994, 8 (20) :2401-2415
[3]
DMC1 - A MEIOSIS-SPECIFIC YEAST HOMOLOG OF ESCHERICHIA-COLI RECA REQUIRED FOR RECOMBINATION, SYNAPTONEMAL COMPLEX-FORMATION, AND CELL-CYCLE PROGRESSION [J].
BISHOP, DK ;
PARK, D ;
XU, LZ ;
KLECKNER, N .
CELL, 1992, 69 (03) :439-456
[4]
BIPARTITE STRUCTURE OF AN EARLY MEIOTIC UPSTREAM ACTIVATION SEQUENCE FROM SACCHAROMYCES-CEREVISIAE [J].
BOWDISH, KS ;
MITCHELL, AP .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (04) :2172-2181
[5]
Special HATs for special occasions: Linking histone acetylation to chromatin assembly and gene activation [J].
Brownell, JE ;
Allis, CD .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1996, 6 (02) :176-184
[6]
CONNECTIONS BETWEEN TRANSCRIPTIONAL ACTIVATORS, SILENCERS, AND TELOMERES AS REVEALED BY FUNCTIONAL-ANALYSIS OF A YEAST DNA-BINDING PROTEIN [J].
BUCHMAN, AR ;
LUE, NF ;
KORNBERG, RD .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (12) :5086-5099
[7]
NUCLEOTIDE-SEQUENCE AND PROMOTER ANALYSIS OF SPO13, A MEIOSIS-SPECIFIC GENE OF SACCHAROMYCES-CEREVISIAE [J].
BUCKINGHAM, LE ;
WANG, HT ;
ELDER, RT ;
MCCARROLL, RM ;
SLATER, MR ;
ESPOSITO, RE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (23) :9406-9410
[8]
CAPIEAUX E, 1989, J BIOL CHEM, V264, P7437
[9]
TRANSCRIPTIONAL CONTROL OF THE SACCHAROMYCES-CEREVISIAE PGK GENE BY RAP1 [J].
CHAMBERS, A ;
TSANG, JSH ;
STANWAY, C ;
KINGSMAN, AJ ;
KINGSMAN, SM .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (12) :5516-5524
[10]
The transcriptional program of sporulation in budding yeast [J].
Chu, S ;
DeRisi, J ;
Eisen, M ;
Mulholland, J ;
Botstein, D ;
Brown, PO ;
Herskowitz, I .
SCIENCE, 1998, 282 (5389) :699-705