Literature DB >> 2196447

Structure and molecular analysis of RGR1, a gene required for glucose repression of Saccharomyces cerevisiae.

A Sakai1, Y Shimizu, S Kondou, T Chibazakura, F Hishinuma.   

Abstract

An RGR1 gene product is required to repress expression of glucose-regulated genes in Saccharomyces cerevisiae. The abnormal morphology of rgr1 cells was studied. Scanning and transmission electron microscopic observations revealed that the cell wall of the daughter cell remained attached to that of mother cell. We cloned the RGR1 gene by complementation and showed that the cloned DNA was tightly linked to the chromosomal RGR1 locus. The cloned RGR1 gene suppressed all of the phenotypes caused by the mutation and encoded a 3.6-kilobase poly(A)+ RNA. The RGR1 gene is located on chromosome XII, as determined by pulsed-field gel electrophoresis, and we mapped rgr1 between gal2 and pep3 by genetic analysis. rgr1 was shown to be a new locus. We also determined the nucleotide sequence of RGR1, which was predicted to encode a 123-kilodalton protein. The null mutation resulted in lethality, indicating that the RGR1 gene is essential for growth. On the other hand, a carboxy-terminal deletion of the gene caused phenotypes similar to but more severe than those caused by the original mutation. The amount of reserve carbohydrates was reduced in rgr1 cells. Possible functions of the RGR1 product are discussed.

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Year:  1990        PMID: 2196447      PMCID: PMC360937          DOI: 10.1128/mcb.10.8.4130-4138.1990

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  20 in total

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Authors:  A Sakai; Y Shimizu; F Hishinuma
Journal:  Genetics       Date:  1988-07       Impact factor: 4.562

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5.  Studies on transformation of Escherichia coli with plasmids.

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7.  An electrophoretic karyotype for yeast.

Authors:  G F Carle; M V Olson
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8.  Regulation of yeast phosphorylase by phosphorylase kinase and cAMP-dependent protein kinase.

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9.  Genetic and biochemical evidence that trehalase is a substrate of cAMP-dependent protein kinase in yeast.

Authors:  I Uno; K Matsumoto; K Adachi; T Ishikawa
Journal:  J Biol Chem       Date:  1983-09-25       Impact factor: 5.157

10.  Reserve carbohydrate metabolism in Saccharomyces cerevisiae: responses to nutrient limitation.

Authors:  S H Lillie; J R Pringle
Journal:  J Bacteriol       Date:  1980-09       Impact factor: 3.490

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  40 in total

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2.  Control of mRNA turnover as a mechanism of glucose repression in Saccharomyces cerevisiae.

Authors:  A Lombardo; G P Cereghino; I E Scheffler
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6.  Requirement for a functional interaction between mediator components Med6 and Srb4 in RNA polymerase II transcription.

Authors:  Y C Lee; Y J Kim
Journal:  Mol Cell Biol       Date:  1998-09       Impact factor: 4.272

7.  Mediator Is Essential for Small Nuclear and Nucleolar RNA Transcription in Yeast.

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8.  Spe3, which encodes spermidine synthase, is required for full repression through NRE(DIT) in Saccharomyces cerevisiae.

Authors:  H Friesen; J C Tanny; J Segall
Journal:  Genetics       Date:  1998-09       Impact factor: 4.562

9.  Regulation of nuclear genes encoding mitochondrial proteins in Saccharomyces cerevisiae.

Authors:  T A Brown; C Evangelista; B L Trumpower
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10.  Promoter-dependent roles for the Srb10 cyclin-dependent kinase and the Hda1 deacetylase in Tup1-mediated repression in Saccharomyces cerevisiae.

Authors:  Sarah R Green; Alexander D Johnson
Journal:  Mol Biol Cell       Date:  2004-07-07       Impact factor: 4.138

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