Literature DB >> 1330823

SPT4, SPT5 and SPT6 interactions: effects on transcription and viability in Saccharomyces cerevisiae.

M S Swanson1, F Winston.   

Abstract

The SPT4, SPT5 and SPT6 genes of Saccharomyces cerevisiae were identified originally by mutations that suppress delta insertion mutations at HIS4 and LYS2. Subsequent analysis has demonstrated that spt4, spt5 and spt6 mutations confer similar pleiotropic phenotypes. They suppress delta insertion mutations by altering transcription and are believed to be required for normal transcription of several other loci. We have now analyzed interactions between SPT4, SPT5 and SPT6. First, the combination of mutations in any two of these three genes causes lethality in haploids. Second, some recessive mutations in different members of this set fail to complement each other. Third, mutations in all three genes alter transcription in similar ways. Finally, the results of coimmunoprecipitation experiments demonstrate that at least the SPT5 and SPT6 proteins interact physically. Taken together, these genetic and biochemical results indicate that SPT4, SPT5 and SPT6 function together in a transcriptional process that is essential for viability in yeast.

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Year:  1992        PMID: 1330823      PMCID: PMC1205139     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  35 in total

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Journal:  J Mol Biol       Date:  1970-02-14       Impact factor: 5.469

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Journal:  Cell       Date:  1986-01-17       Impact factor: 41.582

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Authors:  K D Atkinson
Journal:  Genetics       Date:  1985-09       Impact factor: 4.562

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Authors:  Y Suzuki; Y Nogi; A Abe; T Fukasawa
Journal:  Mol Cell Biol       Date:  1988-11       Impact factor: 4.272

5.  Insertion of the eukaryotic transposable element Ty1 creates a 5-base pair duplication.

Authors:  P J Farabaugh; G R Fink
Journal:  Nature       Date:  1980-07-24       Impact factor: 49.962

6.  Three genes are required for trans-activation of Ty transcription in yeast.

Authors:  F Winston; C Dollard; E A Malone; J Clare; J G Kapakos; P Farabaugh; P L Minehart
Journal:  Genetics       Date:  1987-04       Impact factor: 4.562

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Authors:  D T Chaleff; G R Fink
Journal:  Cell       Date:  1980-08       Impact factor: 41.582

8.  Molecular analysis of SNF2 and SNF5, genes required for expression of glucose-repressible genes in Saccharomyces cerevisiae.

Authors:  E Abrams; L Neigeborn; M Carlson
Journal:  Mol Cell Biol       Date:  1986-11       Impact factor: 4.272

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Authors:  L Neigeborn; K Rubin; M Carlson
Journal:  Genetics       Date:  1986-04       Impact factor: 4.562

10.  Four genes responsible for a position effect on expression from HML and HMR in Saccharomyces cerevisiae.

Authors:  J Rine; I Herskowitz
Journal:  Genetics       Date:  1987-05       Impact factor: 4.562

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  95 in total

Review 1.  Mechanism and regulation of transcriptional elongation by RNA polymerase II.

Authors:  D Reines; R C Conaway; J W Conaway
Journal:  Curr Opin Cell Biol       Date:  1999-06       Impact factor: 8.382

2.  Transcription elongation factor hSPT5 stimulates mRNA capping.

Authors:  Y Wen; A J Shatkin
Journal:  Genes Dev       Date:  1999-07-15       Impact factor: 11.361

3.  Functional interaction between pleiotropic transactivator pUL69 of human cytomegalovirus and the human homolog of yeast chromatin regulatory protein SPT6.

Authors:  M Winkler; T aus Dem Siepen; T Stamminger
Journal:  J Virol       Date:  2000-09       Impact factor: 5.103

4.  In vivo evidence that defects in the transcriptional elongation factors RPB2, TFIIS, and SPT5 enhance upstream poly(A) site utilization.

Authors:  Yajun Cui; Clyde L Denis
Journal:  Mol Cell Biol       Date:  2003-11       Impact factor: 4.272

5.  The cellular protein SPT6 is required for efficient replication of human cytomegalovirus.

Authors:  Daniel Cygnar; Stacy Hagemeier; Daniel Kronemann; Wade A Bresnahan
Journal:  J Virol       Date:  2011-12-14       Impact factor: 5.103

6.  The role of the SPT6 chromatin remodeling factor in zebrafish embryogenesis.

Authors:  Fatma O Kok; Emma Oster; Laura Mentzer; Jen-Chih Hsieh; Clarissa A Henry; Howard I Sirotkin
Journal:  Dev Biol       Date:  2007-05-03       Impact factor: 3.582

7.  Genetic and molecular characterization of GAL83: its interaction and similarities with other genes involved in glucose repression in Saccharomyces cerevisiae.

Authors:  J R Erickson; M Johnston
Journal:  Genetics       Date:  1993-11       Impact factor: 4.562

8.  Mutations that suppress the deletion of an upstream activating sequence in yeast: involvement of a protein kinase and histone H3 in repressing transcription in vivo.

Authors:  G Prelich; F Winston
Journal:  Genetics       Date:  1993-11       Impact factor: 4.562

9.  Bur1 kinase is required for efficient transcription elongation by RNA polymerase II.

Authors:  Michael-Christopher Keogh; Vladimir Podolny; Stephen Buratowski
Journal:  Mol Cell Biol       Date:  2003-10       Impact factor: 4.272

10.  Core histones and HIRIP3, a novel histone-binding protein, directly interact with WD repeat protein HIRA.

Authors:  S Lorain; J P Quivy; F Monier-Gavelle; C Scamps; Y Lécluse; G Almouzni; M Lipinski
Journal:  Mol Cell Biol       Date:  1998-09       Impact factor: 4.272

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