Literature DB >> 2847314

The effect of histone gene deletions on chromatin structure in Saccharomyces cerevisiae.

D Norris1, B Dunn, M A Osley.   

Abstract

As a way of studying nucleosome assembly and maintenance in Saccharomyces cerevisiae, mutants bearing deletions or duplications of the genes encoding histones H2A and H2B were analyzed. Previous genetic analysis had shown that only one of these mutants exhibited dramatic and pleiotropic phenotypes. This mutant was also the only one that contained disrupted chromatin, suggesting that the original phenotypes were attributable to alterations in chromosome structure. The chromatin disruption in the mutant, however, did not extend over the entire genome, but rather was localized to specific regions. Thus, while the arrangement of nucleosomes over the HIS4 and GAL1 genes, the telomeres, and the long terminal repeats (delta sequences) of Ty retrotransposons appeared essentially normal, nucleosomes over the CYH2 and UBI4 genes and the centromere of chromosome III were dramatically disrupted. The observation that the mutant exhibited localized chromatin disruptions implies that the assembly or maintenance of nucleosomes differs over different parts of the yeast genome.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 2847314     DOI: 10.1126/science.2847314

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  29 in total

1.  A gene-specific requirement for FACT during transcription is related to the chromatin organization of the transcribed region.

Authors:  Silvia Jimeno-González; Fernando Gómez-Herreros; Paula M Alepuz; Sebastián Chávez
Journal:  Mol Cell Biol       Date:  2006-09-25       Impact factor: 4.272

2.  Contribution of Trf4/5 and the nuclear exosome to genome stability through regulation of histone mRNA levels in Saccharomyces cerevisiae.

Authors:  Clara C Reis; Judith L Campbell
Journal:  Genetics       Date:  2006-12-18       Impact factor: 4.562

3.  Functional analysis of histones H2A and H2B in transcriptional repression in Saccharomyces cerevisiae.

Authors:  J Recht; B Dunn; A Raff; M A Osley
Journal:  Mol Cell Biol       Date:  1996-06       Impact factor: 4.272

4.  Mutations in both the structured domain and N-terminus of histone H2B bypass the requirement for Swi-Snf in yeast.

Authors:  J Recht; M A Osley
Journal:  EMBO J       Date:  1999-01-04       Impact factor: 11.598

5.  A novel histone H4 mutant defective in nuclear division and mitotic chromosome transmission.

Authors:  M M Smith; P Yang; M S Santisteban; P W Boone; A T Goldstein; P C Megee
Journal:  Mol Cell Biol       Date:  1996-03       Impact factor: 4.272

6.  Histone octamer function in vivo: mutations in the dimer-tetramer interfaces disrupt both gene activation and repression.

Authors:  M S Santisteban; G Arents; E N Moudrianakis; M M Smith
Journal:  EMBO J       Date:  1997-05-01       Impact factor: 11.598

7.  Amplification of histone genes by circular chromosome formation in Saccharomyces cerevisiae.

Authors:  Diana E Libuda; Fred Winston
Journal:  Nature       Date:  2006-10-26       Impact factor: 49.962

8.  Analysis of yeast retrotransposon Ty insertions at the CAN1 locus.

Authors:  C M Wilke; S H Heidler; N Brown; S W Liebman
Journal:  Genetics       Date:  1989-12       Impact factor: 4.562

9.  SPT10 and SPT21 are required for transcription of particular histone genes in Saccharomyces cerevisiae.

Authors:  C Dollard; S L Ricupero-Hovasse; G Natsoulis; J D Boeke; F Winston
Journal:  Mol Cell Biol       Date:  1994-08       Impact factor: 4.272

10.  Sth1p, a Saccharomyces cerevisiae Snf2p/Swi2p homolog, is an essential ATPase in RSC and differs from Snf/Swi in its interactions with histones and chromatin-associated proteins.

Authors:  J Du; I Nasir; B K Benton; M P Kladde; B C Laurent
Journal:  Genetics       Date:  1998-11       Impact factor: 4.562

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.