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The Four Causes: The Functional Architecture of Centromeres and Kinetochores.
McAinsh, Andrew D; Marston, Adele L.
Affiliation
  • McAinsh AD; Centre for Mechanochemical Cell Biology, University of Warwick, Coventry, United Kingdom; email: A.D.McAinsh@warwick.ac.uk.
  • Marston AL; Division of Biomedical Sciences, Warwick Medical School, University of Warwick, Coventry, United Kingdom.
Annu Rev Genet ; 56: 279-314, 2022 11 30.
Article in En | MEDLINE | ID: mdl-36055650
ABSTRACT
Kinetochores are molecular machines that power chromosome segregation during the mitotic and meiotic cell divisions of all eukaryotes. Aristotle explains how we think we have knowledge of a thing only when we have grasped its cause. In our case, to gain understanding of the kinetochore, the four causes correspond to questions that we must ask (a) What are the constituent parts, (b) how does it assemble, (c) what is the structure and arrangement, and (d) what is the function? Here we outline the current blueprint for the assembly of a kinetochore, how functions are mapped onto this architecture, and how this is shaped by the underlying pericentromeric chromatin. The view of the kinetochore that we present is possible because an almost complete parts list of the kinetochore is now available alongside recent advances using in vitro reconstitution, structural biology, and genomics. In many organisms, each kinetochore binds to multiple microtubules, and we propose a model for how this ensemble-level architecture is organized, drawing on key insights from the simple one microtubule-one kinetochore setup in budding yeast and innovations that enable meiotic chromosome segregation.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Centromere / Kinetochores Type of study: Etiology_studies Language: En Journal: Annu Rev Genet Year: 2022 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Centromere / Kinetochores Type of study: Etiology_studies Language: En Journal: Annu Rev Genet Year: 2022 Type: Article