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PMID: 10626889 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Rapid and selective remodeling of a positioned nucleosome during the induction of IL-12 p40 transcription.

Immunity ·Vol. 11 ·No. 6 ·1999-12-00 ·Pages 665-75

Weinmann AS, Plevy SE, Smale ST

Abstract

Nucleosomes are important for gene regulation, but comprehensive studies of nucleosome positioning, remodeling, and transcription factor binding at inducible mammalian promoters have not been reported. We have analyzed the IL-12 p40 promoter, which is induced in macrophages by bacterial products. High-resolution micrococcal nuclease analyses revealed that a positioned nucleosome, nucleosome 1, spans the promoter, with three positioned nucleosomes further upstream. Upon activation, nucleosome 1 was rapidly and selectively remodeled in a protein synthesis-dependent manner. In primary macrophages, IFNgamma synergistically enhanced p40 expression, but little effect on remodeling or promoter occupancy was observed. These results suggest that remodeling complexes are selectively targeted to a single, promoter-encompassing nucleosome and that IFNgamma influences an event that is independent or downstream of remodeling.

MeSH Terms
Animals Cell Line Cells, Cultured Gene Expression Interleukin-12/genetics Macrophages/cytology Mice Mice, Inbred C57BL Micrococcal Nuclease/metabolism Nucleosomes/metabolism Promoter Regions, Genetic Time Factors Transcription, Genetic
Chemicals
Nucleosomes Interleukin-12 Micrococcal Nuclease
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Weinmann A S
Howard Hughes Medical Institute, Department of Microbiology, Immunology, and Molecular Genetics, University of California, 90095-1662, USA.
Plevy S E
Smale S T
Article Info
Journal
Immunity
Abbr.
Immunity
ISSN
1074-7613
Published
1999-12-00
Pages
665-75
Language
English
Region
United States
NLM ID
9432918
Subset
IM
Grants
NIGMS NIH HHS · GM07185 · United States
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