Models for the architecture of the human inner kinetochore on centromeric α-satellite CENP-A nucleosome arrays

Human kinetochores assemble onto centromeric DNA comprising repetitive arrays of the 171 bp α-satellite sequence. To understand the higher-order architecture of the inner kinetochore assembled onto α-satellite arrays, we show cryo-EM structures of CCAN with free DNA, and α-satellite repeat monomers and dimers with CENP-A nucleosomes. CCAN bound to free DNA and a monomeric CENP-A nucleosome engages 70 bp of DNA comprising 30 bp of an upstream α-satellite repeat. This upstream DNA interacts with the histone-fold domain subunits of the CENP-TWSX module in a manner resembling how nucleosomes wrap DNA gyres. A complex of CCAN assembled onto a dimeric α-satellite repeat with two CENP-A nucleosomes shows that CCAN can only be accommodated on the linker DNA by unwrapping DNA from both the CENP-TWSX module and the upstream nucleosome. We discuss the implications of these results for models of CCAN assembly on arrays of α-satellite chromatin containing CENP-A nucleosomes.

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Journal
Nature Communications
Published
2026-05-12
DOI
https://doi.org/10.1038/s41467-026-72856-0
Primary Topic
Microtubule and mitosis dynamics
Type
article
Field-Weighted Citation Impact
0.00

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article

Models for the architecture of the human inner kinetochore on centromeric α-satellite CENP-A nucleosome arrays

Stephen H. McLaughlin, Kyle Muir, Cong Yu, Ziguo Zhang et al.
Nature Communications
Microtubule and mitosis dynamics
article

Models for the architecture of the human inner kinetochore on centromeric α-satellite CENP-A nucleosome arrays

Stephen H. McLaughlin, Kyle Muir, Cong Yu, Ziguo Zhang, David Barford, Jing Yang
article en

Abstract

Human kinetochores assemble onto centromeric DNA comprising repetitive arrays of the 171 bp α-satellite sequence. To understand the higher-order architecture of the inner kinetochore assembled onto α-satellite arrays, we show cryo-EM structures of CCAN with free DNA, and α-satellite repeat monomers and dimers with CENP-A nucleosomes. CCAN bound to free DNA and a monomeric CENP-A nucleosome engages 70 bp of DNA comprising 30 bp of an upstream α-satellite repeat. This upstream DNA interacts with the histone-fold domain subunits of the CENP-TWSX module in a manner resembling how nucleosomes wrap DNA gyres. A complex of CCAN assembled onto a dimeric α-satellite repeat with two CENP-A nucleosomes shows that CCAN can only be accommodated on the linker DNA by unwrapping DNA from both the CENP-TWSX module and the upstream nucleosome. We discuss the implications of these results for models of CCAN assembly on arrays of α-satellite chromatin containing CENP-A nucleosomes.

Nature Communications
MRC Laboratory of Molecular Biology (GB), The Francis Crick Institute (GB), University of Edinburgh (GB)
Cancer Research UK
Openalex Percentile: Top 8%
Microtubule and mitosis dynamics
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Models for the architecture of the human inner kinetochore on centromeric α-satellite CENP-A nucleosome arrays — Stephen H. McLaughlin, Kyle Muir, et al. · Nature Communications (2026) | TGRS Research Map | TGRS