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PMID: 8232556 Published · ppublish English Journal Article

BRG1 contains a conserved domain of the SWI2/SNF2 family necessary for normal mitotic growth and transcription.

Nature ·Vol. 366 ·No. 6451 ·1993-11-11 ·Pages 170-4

Khavari PA, Peterson CL, Tamkun JW, Mendel DB, Crabtree GR

Abstract

Sequence-specific DNA binding activators of gene transcription may be assisted by SWI2 (SNF2), which contains a DNA-dependent ATPase domain. We have isolated a human complementary DNA encoding a 205K nuclear protein, BRG1, that contains extensive homology to SWI2 and Drosophila brahma. We report here that a SWI2/BRG1 chimera with the DNA-dependent ATPase domain replaced by corresponding human sequence restored normal mitotic growth and capacity for transcriptional activation to swi2- yeast cells. Point mutation of the conserved ATP binding site lysine abolished this complementation. This mutation in SWI2 exerted a dominant negative effect on transcription in yeast. A lysine to arginine substitution at the corresponding residue of BRG1 also generated a transcriptional dominant negative in human cells. BRG1 is exclusively nuclear and present in a high M(r) complex of about 2 x 10(6). These results show that the SWI2 family DNA-dependent ATPase domain has functional conservation between yeast and humans and suggest that a SWI/SNF protein complex is required for the activation of selective mammalian genes.

Related Genes
MeSH Terms
Adenosine Triphosphatases/genetics,metabolism Adenosine Triphosphate/metabolism Amino Acid Sequence Base Sequence DNA Helicases DNA-Binding Proteins/genetics,metabolism Genetic Complementation Test HeLa Cells Humans Mitosis Molecular Sequence Data Nuclear Proteins/genetics,metabolism Organ Specificity Point Mutation Recombinant Fusion Proteins/genetics,metabolism Saccharomyces cerevisiae/genetics Saccharomyces cerevisiae Proteins Sequence Homology, Amino Acid Transcription Factors/genetics,metabolism Transcription, Genetic
Chemicals
DNA-Binding Proteins Nuclear Proteins Recombinant Fusion Proteins SMARCA1 protein, human SMARCA2 protein, human Saccharomyces cerevisiae Proteins Transcription Factors Adenosine Triphosphate Adenosine Triphosphatases SMARCA4 protein, human SNF2 protein, S cerevisiae DNA Helicases
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Khavari P A
Howard Hughes Medical Institute, Stanford University, California 94305.
Peterson C L
Tamkun J W
Mendel D B
Crabtree G R
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1993-11-11
Pages
170-4
Language
English
Region
England
NLM ID
0410462
Subset
IM
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