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ATP-dependent chromatin remodeling enzymes: two heads are not better, just different

Journal

CURRENT OPINION IN GENETICS & DEVELOPMENT
Volume 18, Issue 2, Pages 137-144

Publisher

CURRENT BIOLOGY LTD
DOI: 10.1016/j.gde.2008.01.007

Keywords

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Funding

  1. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM073767] Funding Source: NIH RePORTER
  2. NIGMS NIH HHS [R01 GM073767-03, R01 GM073767-04, R01 GM073767] Funding Source: Medline

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ATP-dependent chromatin remodeling complexes enable rapid rearrangements in chromatin structure in response to developmental cues. The ATPase subunits of remodeling complexes share homology with the helicase motifs of DExx box helicases. Recent single-molecule experiments indicate that, like helicases, many of these complexes use ATP to translocate on DNA. Despite sharing this fundamental property, two key classes of remodeling complexes, the ISWI class and the SWI/SNF class, generate distinct remodeled products. SWI/SNF complexes generate nucleosomes with altered positions, nucleosomes with DNA loops and nucleosomes that are capable of exchanging histone dimers or octamers. In contrast, ISWI complexes generate nucleosomes with altered positions but in standard structures. Here, we draw analogies to monomeric and dimeric helicases and propose that ISWI and SWI/SNF complexes catalyze different outcomes in part because some ISWI complexes function as dimers while SWI/SNF complexes function as monomers.

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