Literature DB >> 10586882

Chromosomal landscape of nucleosome-dependent gene expression and silencing in yeast.

J J Wyrick1, F C Holstege, E G Jennings, H C Causton, D Shore, M Grunstein, E S Lander, R A Young.   

Abstract

Eukaryotic genomes are packaged into nucleosomes, which are thought to repress gene expression generally. Repression is particularly evident at yeast telomeres, where genes within the telomeric heterochromatin appear to be silenced by the histone-binding silent information regulator (SIR) complex (Sir2, Sir3, Sir4) and Rap1 (refs 4-10). Here, to investigate how nucleosomes and silencing factors influence global gene expression, we use high-density arrays to study the effects of depleting nucleosomal histones and silencing factors in yeast. Reducing nucleosome content by depleting histone H4 caused increased expression of 15% of genes and reduced expression of 10% of genes, but it had little effect on expression of the majority (75%) of yeast genes. Telomere-proximal genes were found to be de-repressed over regions extending 20 kilobases from the telomeres, well beyond the extent of Sir protein binding and the effects of loss of Sir function. These results indicate that histones make Sir-independent contributions to telomeric silencing, and that the role of histones located elsewhere in chromosomes is gene specific rather than generally repressive.

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Year:  1999        PMID: 10586882     DOI: 10.1038/46567

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  181 in total

1.  Histone acetylation at promoters is differentially affected by specific activators and repressors.

Authors:  J Deckert; K Struhl
Journal:  Mol Cell Biol       Date:  2001-04       Impact factor: 4.272

2.  Targeted histone acetylation and altered nuclease accessibility over short regions of the pea plastocyanin gene.

Authors:  Y L Chua; A P Brown; J C Gray
Journal:  Plant Cell       Date:  2001-03       Impact factor: 11.277

Review 3.  Nuclear position leaves its mark on replication timing.

Authors:  D M Gilbert
Journal:  J Cell Biol       Date:  2001-01-22       Impact factor: 10.539

4.  H2A.Z is required for global chromatin integrity and for recruitment of RNA polymerase II under specific conditions.

Authors:  M Adam; F Robert; M Larochelle; L Gaudreau
Journal:  Mol Cell Biol       Date:  2001-09       Impact factor: 4.272

5.  Hyperacetylation of chromatin at the ADH2 promoter allows Adr1 to bind in repressed conditions.

Authors:  Loredana Verdone; Jiansheng Wu; Kristen van Riper; Nataly Kacherovsky; Maria Vogelauer; Elton T Young; Michael Grunstein; Ernesto Di Mauro; Micaela Caserta
Journal:  EMBO J       Date:  2002-03-01       Impact factor: 11.598

6.  BUR1 and BUR2 encode a divergent cyclin-dependent kinase-cyclin complex important for transcription in vivo.

Authors:  S Yao; A Neiman; G Prelich
Journal:  Mol Cell Biol       Date:  2000-10       Impact factor: 4.272

7.  Collaborative competition mechanism for gene activation in vivo.

Authors:  Joanna A Miller; Jonathan Widom
Journal:  Mol Cell Biol       Date:  2003-03       Impact factor: 4.272

8.  A genomic model of condition-specific nucleosome behavior explains transcriptional activity in yeast.

Authors:  Judith B Zaugg; Nicholas M Luscombe
Journal:  Genome Res       Date:  2011-09-19       Impact factor: 9.043

9.  Genomewide studies of histone deacetylase function in yeast.

Authors:  B E Bernstein; J K Tong; S L Schreiber
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-05       Impact factor: 11.205

10.  Direct stimulation of transcription by negative cofactor 2 (NC2) through TATA-binding protein (TBP).

Authors:  Yong Cang; Gregory Prelich
Journal:  Proc Natl Acad Sci U S A       Date:  2002-09-17       Impact factor: 11.205

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