Recruitment of two Ndc80 complexes via the CENP-T pathway is sufficient for kinetochore functions

Yusuke Takenoshita, Masatoshi Hara and Tatsuo Fukagawa ()
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Yusuke Takenoshita: Osaka University
Masatoshi Hara: Osaka University
Tatsuo Fukagawa: Osaka University

Nature Communications, 2022, vol. 13, issue 1, 1-19

Abstract: Abstract To form functional kinetochores, CENP-C and CENP-T independently recruit the KMN (Knl1C, Mis12C, and Ndc80C) network onto the kinetochores. To clarify the functions of the KMN network on CENP-T, we evaluated its roles in chicken DT40 cell lines lacking the CENP-C-KMN network interaction. By analyzing mutants lacking both CENP-T-Mis12C and CENP-C-Mis12C interactions, we demonstrated that Knl1C and Mis12C (KM) play critical roles in the cohesion of sister chromatids or the recruitment of spindle checkpoint proteins onto kinetochores. Two copies of Ndc80C (N-N) exist on CENP-T via Mis12C or direct binding. Analyses of cells specifically lacking the Mis12C-Ndc80C interaction revealed that N-N is needed for proper kinetochore-microtubule interactions. However, using artificial engineering to directly bind the two copies of Ndc80C to CENP-T, we demonstrated that N-N functions without direct Mis12C binding to Ndc80C in native kinetochores. This study demonstrated the mechanisms by which complicated networks play roles in native kinetochores.

Date: 2022
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DOI: 10.1038/s41467-022-28403-8

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