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Targeting Polo-like kinase in space and time during C. elegans meiosis

A central player in meiotic chromosome dynamics is the conserved Polo-like kinase (PLK) family. PLKs are dynamically localized to distinct structures during meiotic prophase and phosphorylate a diverse group of substrates to control homolog pairing, synapsis, and meiotic recombination. In a recent s...

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Autores principales: Brandt, James N., Kim, Yumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432353/
https://www.ncbi.nlm.nih.gov/pubmed/34266376
http://dx.doi.org/10.1080/15384101.2021.1953232
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author Brandt, James N.
Kim, Yumi
author_facet Brandt, James N.
Kim, Yumi
author_sort Brandt, James N.
collection PubMed
description A central player in meiotic chromosome dynamics is the conserved Polo-like kinase (PLK) family. PLKs are dynamically localized to distinct structures during meiotic prophase and phosphorylate a diverse group of substrates to control homolog pairing, synapsis, and meiotic recombination. In a recent study, we uncovered the mechanisms that control the targeting of a meiosis-specific PLK-2 in C. elegans. In early meiotic prophase, PLK-2 localizes to special chromosome regions known as pairing centers and drives homolog pairing and synapsis. PLK-2 then relocates to the synaptonemal complex (SC) after crossover designation and mediates chromosome remodeling required for homolog separation. What controls this intricate targeting of PLK-2 in space and time? We discuss recent findings and remaining questions for the future.
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spelling pubmed-84323532021-09-11 Targeting Polo-like kinase in space and time during C. elegans meiosis Brandt, James N. Kim, Yumi Cell Cycle Review A central player in meiotic chromosome dynamics is the conserved Polo-like kinase (PLK) family. PLKs are dynamically localized to distinct structures during meiotic prophase and phosphorylate a diverse group of substrates to control homolog pairing, synapsis, and meiotic recombination. In a recent study, we uncovered the mechanisms that control the targeting of a meiosis-specific PLK-2 in C. elegans. In early meiotic prophase, PLK-2 localizes to special chromosome regions known as pairing centers and drives homolog pairing and synapsis. PLK-2 then relocates to the synaptonemal complex (SC) after crossover designation and mediates chromosome remodeling required for homolog separation. What controls this intricate targeting of PLK-2 in space and time? We discuss recent findings and remaining questions for the future. Taylor & Francis 2021-07-16 /pmc/articles/PMC8432353/ /pubmed/34266376 http://dx.doi.org/10.1080/15384101.2021.1953232 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Review
Brandt, James N.
Kim, Yumi
Targeting Polo-like kinase in space and time during C. elegans meiosis
title Targeting Polo-like kinase in space and time during C. elegans meiosis
title_full Targeting Polo-like kinase in space and time during C. elegans meiosis
title_fullStr Targeting Polo-like kinase in space and time during C. elegans meiosis
title_full_unstemmed Targeting Polo-like kinase in space and time during C. elegans meiosis
title_short Targeting Polo-like kinase in space and time during C. elegans meiosis
title_sort targeting polo-like kinase in space and time during c. elegans meiosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432353/
https://www.ncbi.nlm.nih.gov/pubmed/34266376
http://dx.doi.org/10.1080/15384101.2021.1953232
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