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Cryoelectron Microscopy Structure of a Yeast Centromeric Nucleosome at 2.7 Å Resolution.

Authors :
Migl D
Kschonsak M
Arthur CP
Khin Y
Harrison SC
Ciferri C
Dimitrova YN
Source :
Structure (London, England : 1993) [Structure] 2020 Mar 03; Vol. 28 (3), pp. 363-370.e3. Date of Electronic Publication: 2020 Jan 30.
Publication Year :
2020

Abstract

Kinetochores mediate chromosome segregation during cell division. They assemble on centromeric nucleosomes and capture spindle microtubules. In budding yeast, a kinetochore links a single nucleosome, containing the histone variant Cse4 <superscript>CENP-A</superscript> instead of H3, with a single microtubule. Conservation of most kinetochore components from yeast to metazoans suggests that the yeast kinetochore represents a module of the more complex metazoan arrangements. We describe here a streamlined protocol for reconstituting a yeast centromeric nucleosome and a systematic exploration of cryo-grid preparation. These developments allowed us to obtain a high-resolution cryoelectron microscopy reconstruction. As suggested by previous work, fewer base pairs are in tight association with the histone octamer than there are in canonical nucleosomes. Weak binding of the end DNA sequences may contribute to specific recognition by other inner kinetochore components. The centromeric nucleosome structure and the strategies we describe will facilitate studies of many other aspects of kinetochore assembly and chromatin biochemistry.<br />Competing Interests: Declaration of Interests The authors declare no competing interests.<br /> (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1878-4186
Volume :
28
Issue :
3
Database :
MEDLINE
Journal :
Structure (London, England : 1993)
Publication Type :
Academic Journal
Accession number :
32004465
Full Text :
https://doi.org/10.1016/j.str.2019.12.002