4.7 Article

Cryo-EM structures of the human INO80 chromatin-remodeling complex

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NATURE STRUCTURAL & MOLECULAR BIOLOGY
卷 25, 期 1, 页码 37-+

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41594-017-0003-7

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  1. Wellcome Trust [098412/Z/12/Z, 095519/Z/11/Z]
  2. Cancer Research UK [C6913/A21608]
  3. Wellcome Trust [095519/Z/11/Z, 098412/Z/12/Z] Funding Source: Wellcome Trust
  4. Cancer Research UK [12799] Funding Source: researchfish
  5. Wellcome Trust [098412/Z/12/Z] Funding Source: researchfish

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Access to chromatin for processes such as transcription and DNA repair requires the sliding of nucleosomes along DNA. This process is aided by chromatin-remodeling complexes, such as the multisubunit INO80 chromatin-remodeling complex. Here we present cryo-EM structures of the active core complex of human INO80 at 9.6 angstrom, with portions at 4.1-angstrom resolution, and reconstructions of combinations of subunits. Together, these structures reveal the architecture of the INO80 complex, including Ino80 and actin-related proteins, which is assembled around a single RUVBL1 (Tip49a) and RUVBL2 (Tip49b) AAA+ heterohexamer. An unusual spoked-wheel structural domain of the Ino80 subunit is engulfed by this heterohexamer; both, in combination, form the core of the complex. We also identify a cleft in RUVBL1 and RUVBL2, which forms a major interaction site for partner proteins and probably communicates these interactions to its nucleotide-binding sites.

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