A GENERAL SUPPRESSOR OF RNA POLYMERASE-I, POLYMERASE-II AND POLYMERASE-III MUTATIONS IN SACCHAROMYCES-CEREVISIAE
被引:83
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作者:
STETTLER, S
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机构:CTR ETUD SACLAY, CEA,DEPT BIOL CELLULAIRE & MOLEC, SERV BIOCHIM & GENET MOLEC,BAT 142, F-91191 GIF SUR YVETTE, FRANCE
STETTLER, S
CHIANNILKULCHAI, N
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机构:CTR ETUD SACLAY, CEA,DEPT BIOL CELLULAIRE & MOLEC, SERV BIOCHIM & GENET MOLEC,BAT 142, F-91191 GIF SUR YVETTE, FRANCE
CHIANNILKULCHAI, N
DENMAT, SHL
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机构:CTR ETUD SACLAY, CEA,DEPT BIOL CELLULAIRE & MOLEC, SERV BIOCHIM & GENET MOLEC,BAT 142, F-91191 GIF SUR YVETTE, FRANCE
DENMAT, SHL
LALO, D
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机构:CTR ETUD SACLAY, CEA,DEPT BIOL CELLULAIRE & MOLEC, SERV BIOCHIM & GENET MOLEC,BAT 142, F-91191 GIF SUR YVETTE, FRANCE
LALO, D
LACROUTE, F
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机构:CTR ETUD SACLAY, CEA,DEPT BIOL CELLULAIRE & MOLEC, SERV BIOCHIM & GENET MOLEC,BAT 142, F-91191 GIF SUR YVETTE, FRANCE
LACROUTE, F
SENTENAC, A
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SENTENAC, A
THURIAUX, P
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机构:CTR ETUD SACLAY, CEA,DEPT BIOL CELLULAIRE & MOLEC, SERV BIOCHIM & GENET MOLEC,BAT 142, F-91191 GIF SUR YVETTE, FRANCE
THURIAUX, P
机构:
[1] CTR ETUD SACLAY, CEA,DEPT BIOL CELLULAIRE & MOLEC, SERV BIOCHIM & GENET MOLEC,BAT 142, F-91191 GIF SUR YVETTE, FRANCE
[2] UNIV PARIS 06, LAB ASSOCIE, CNRS, CTR GENET MOLEC, F-75230 PARIS 05, FRANCE
来源:
MOLECULAR AND GENERAL GENETICS
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1993年
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239卷
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1-2期
关键词:
PROTEIN PHOSPHORYLATION;
PHOSPHATASE;
CYCLIC AMP;
RNA POLYMERASE;
TRANSCRIPTION;
D O I:
10.1007/BF00281615
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:
A multicopy genomic library of Saccharomyces cerevisiae (strain FL100) was screened for its ability to suppress conditionally defective mutations altering the 31 kDa subunit (rpc31-236) or the 53 kDa subunit (rpc53-254/424) of RNA polymerase III. In addition to allele-specific suppressors, we identified seven suppressor clones that acted on both mutations and also suppressed several other conditional mutations defective in RNA polymerases I or II. All these clones harbored a complete copy of the SSD1 gene. The same pleiotropic suppression pattern was found with the dominant SSD1-v allele present in some laboratory strains of S. cerevisiae. SSD1-v was previously shown to suppress mutations defective in the SIT4 gene product (a predicted protein phosphatase subunit) or in the regulatory subunit of the cyclic AMP-dependent protein kinase. We propose that the SSD1 gene product modulates the activity (or the level) of the three nuclear RNA polymerases, possibly by altering their degree of phosphorylation.