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STARD9/Kif16a is a novel mitotic kinesin and antimitotic target

Proper cell division requires the formation of the microtubule-based mitotic spindle, which mediates the dynamic movement and alignment of chromosomes to the metaphase plate and their equal transmission to daughter cells. Kinesins are molecular motors that utilize ATP hydrolysis to perform their fun...

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Detalles Bibliográficos
Autor principal: Torres, Jorge Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3383713/
https://www.ncbi.nlm.nih.gov/pubmed/22754624
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author Torres, Jorge Z.
author_facet Torres, Jorge Z.
author_sort Torres, Jorge Z.
collection PubMed
description Proper cell division requires the formation of the microtubule-based mitotic spindle, which mediates the dynamic movement and alignment of chromosomes to the metaphase plate and their equal transmission to daughter cells. Kinesins are molecular motors that utilize ATP hydrolysis to perform their functions and are instrumental in spindle assembly and function. Of the over 45 kinesins encoded in the human genome, only two are specifically enriched at the centrioles, Kif24 at the mother centriole and STARD9/Kif16a at the daughter centriole. While Kif24 possesses centriolar microtubule-depolymerizing activity and has been implicated in regulating cilia formation, our recent study implicates STARD9 in maintaining pericentriolar material (PCM) cohesion during early mitosis. However, very little is known about how STARD9 performs its function, including the mechanisms that recruit or retain STARD9 at the centrioles and how it cooperates with centrosome components to regulate PCM stability. Additionally, the signals leading to apoptosis in the absence of STARD9 remain to be explored.
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spelling pubmed-33837132012-06-29 STARD9/Kif16a is a novel mitotic kinesin and antimitotic target Torres, Jorge Z. Bioarchitecture Commentary Proper cell division requires the formation of the microtubule-based mitotic spindle, which mediates the dynamic movement and alignment of chromosomes to the metaphase plate and their equal transmission to daughter cells. Kinesins are molecular motors that utilize ATP hydrolysis to perform their functions and are instrumental in spindle assembly and function. Of the over 45 kinesins encoded in the human genome, only two are specifically enriched at the centrioles, Kif24 at the mother centriole and STARD9/Kif16a at the daughter centriole. While Kif24 possesses centriolar microtubule-depolymerizing activity and has been implicated in regulating cilia formation, our recent study implicates STARD9 in maintaining pericentriolar material (PCM) cohesion during early mitosis. However, very little is known about how STARD9 performs its function, including the mechanisms that recruit or retain STARD9 at the centrioles and how it cooperates with centrosome components to regulate PCM stability. Additionally, the signals leading to apoptosis in the absence of STARD9 remain to be explored. Landes Bioscience 2012-01-01 /pmc/articles/PMC3383713/ /pubmed/22754624 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Commentary
Torres, Jorge Z.
STARD9/Kif16a is a novel mitotic kinesin and antimitotic target
title STARD9/Kif16a is a novel mitotic kinesin and antimitotic target
title_full STARD9/Kif16a is a novel mitotic kinesin and antimitotic target
title_fullStr STARD9/Kif16a is a novel mitotic kinesin and antimitotic target
title_full_unstemmed STARD9/Kif16a is a novel mitotic kinesin and antimitotic target
title_short STARD9/Kif16a is a novel mitotic kinesin and antimitotic target
title_sort stard9/kif16a is a novel mitotic kinesin and antimitotic target
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3383713/
https://www.ncbi.nlm.nih.gov/pubmed/22754624
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