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PMID: 10842313 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Recruitment of chromatin remodeling machines.

Journal of cellular biochemistry ·Vol. 78 ·No. 2 ·2000-05-00 ·Pages 179-85

Peterson CL, Logie C

Abstract

The assembly of eukaryotic DNA into folded nucleosomal arrays has drastic consequences for many nuclear processes that require access to the DNA sequence, including RNA transcription, DNA replication, recombination, and repair. Two types of highly conserved chromatin remodeling enzymes have been implicated as regulators of the repressive nature of chromatin structure: ATP-dependent remodeling complexes and nuclear histone acetyltransferases (HATs). Recent studies indicate that both types of enzymes can be recruited to chromosomal loci through either physical interactions with transcriptional activators or via the global accessibility of chromatin during S phase of the cell cycle. Here we review these recent observations and discuss the implications for gene-specific regulation by chromatin remodeling machines.

MeSH Terms
Acetyltransferases/metabolism Chromatin/genetics,metabolism DNA, Fungal/genetics,metabolism DNA-Binding Proteins Fungal Proteins/metabolism Gene Expression Regulation, Fungal Histone Acetyltransferases Protein Kinases/metabolism S Phase Saccharomyces cerevisiae/genetics,metabolism Saccharomyces cerevisiae Proteins Trans-Activators/metabolism
Chemicals
Chromatin DNA, Fungal DNA-Binding Proteins Fungal Proteins Saccharomyces cerevisiae Proteins Trans-Activators Acetyltransferases Histone Acetyltransferases Protein Kinases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Peterson C L
Program in Molecular Medicine and Department of Biochemistry and Molecular Biology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA. [email protected]
Logie C
Article Info
Journal
Journal of cellular biochemistry
Abbr.
J Cell Biochem
ISSN
0730-2312
Published
2000-05-00
Pages
179-85
Language
English
Region
United States
NLM ID
8205768
Subset
IM
Grants
NIGMS NIH HHS · GM49650 · United States
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