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Mis16 Switches Function from a Histone H4 Chaperone to a CENP-A-Specific Assembly Factor through Eic1 Interaction. | LitMetric

Mis16 Switches Function from a Histone H4 Chaperone to a CENP-A-Specific Assembly Factor through Eic1 Interaction.

Structure

Department of Biological Chemistry, University of Michigan Medical School, 1150 W. Medical Center Drive, SPC 5606, Ann Arbor, MI 48109, USA; Program in Cellular and Molecular Biology, University of Michigan, Ann Arbor, MI 48109, USA. Electronic address:

Published: July 2018

AI Article Synopsis

Article Abstract

The Mis18 complex, composed of Mis16, Eic1, and Mis18 in fission yeast, selectively deposits the centromere-specific histone H3 variant, CENP-A, at centromeres. How the intact Mis18 holo-complex oligomerizes and how Mis16, a well-known ubiquitous histone H4 chaperone, plays a centromere-specific role in the Mis18 holo-complex, remain unclear. Here, we report the stoichiometry of the intact Mis18 holo-complex as (Mis16):(Eic1):(Mis18) using analytical ultracentrifugation. We further determine the crystal structure of Schizosaccharomyces pombe Mis16 in complex with the C-terminal portion of Eic1 (Eic1-CT). Notably, Mis16 accommodates Eic1-CT through the binding pocket normally occupied by histone H4, indicating that Eic1 and H4 compete for the same binding site, providing a mechanism for Mis16 to switch its binding partner from histone H4 to Eic1. Thus, our analyses not only determine the stoichiometry of the intact Mis18 holo-complex but also uncover the molecular mechanism by which Mis16 plays a centromere-specific role through Eic1 association.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031460PMC
http://dx.doi.org/10.1016/j.str.2018.04.012DOI Listing

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