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

      Nature
      Adenosine Triphosphatases, genetics, metabolism, Adenosine Triphosphate, Amino Acid Sequence, Base Sequence, DNA Helicases, DNA-Binding Proteins, Genetic Complementation Test, HeLa Cells, Humans, Mitosis, Molecular Sequence Data, Nuclear Proteins, Organ Specificity, Point Mutation, Recombinant Fusion Proteins, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Sequence Homology, Amino Acid, Transcription Factors, Transcription, Genetic

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          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.

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