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Tissue-Specific Requirement for the GINS Complex During Zebrafish Development

Efficient and accurate DNA replication is particularly critical in stem and progenitor cells for successful proliferation and survival. The replisome, an amalgam of protein complexes, is responsible for binding potential origins of replication, unwinding the double helix, and then synthesizing compl...

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Autores principales: Varga, Máté, Csályi, Kitti, Bertyák, István, Menyhárd, Dóra K., Poole, Richard J., Cerveny, Kara L., Kövesdi, Dorottya, Barátki, Balázs, Rouse, Hannah, Vad, Zsuzsa, Hawkins, Thomas A., Stickney, Heather L., Cavodeassi, Florencia, Schwarz, Quenten, Young, Rodrigo M., Wilson, Stephen W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7270345/
https://www.ncbi.nlm.nih.gov/pubmed/32548116
http://dx.doi.org/10.3389/fcell.2020.00373
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author Varga, Máté
Csályi, Kitti
Bertyák, István
Menyhárd, Dóra K.
Poole, Richard J.
Cerveny, Kara L.
Kövesdi, Dorottya
Barátki, Balázs
Rouse, Hannah
Vad, Zsuzsa
Hawkins, Thomas A.
Stickney, Heather L.
Cavodeassi, Florencia
Schwarz, Quenten
Young, Rodrigo M.
Wilson, Stephen W.
author_facet Varga, Máté
Csályi, Kitti
Bertyák, István
Menyhárd, Dóra K.
Poole, Richard J.
Cerveny, Kara L.
Kövesdi, Dorottya
Barátki, Balázs
Rouse, Hannah
Vad, Zsuzsa
Hawkins, Thomas A.
Stickney, Heather L.
Cavodeassi, Florencia
Schwarz, Quenten
Young, Rodrigo M.
Wilson, Stephen W.
author_sort Varga, Máté
collection PubMed
description Efficient and accurate DNA replication is particularly critical in stem and progenitor cells for successful proliferation and survival. The replisome, an amalgam of protein complexes, is responsible for binding potential origins of replication, unwinding the double helix, and then synthesizing complimentary strands of DNA. According to current models, the initial steps of DNA unwinding and opening are facilitated by the CMG complex, which is composed of a GINS heterotetramer that connects Cdc45 with the mini-chromosome maintenance (Mcm) helicase. In this work, we provide evidence that in the absence of GINS function DNA replication is cell autonomously impaired, and we also show that gins1 and gins2 mutants exhibit elevated levels of apoptosis restricted to actively proliferating regions of the central nervous system (CNS). Intriguingly, our results also suggest that the rapid cell cycles during early embryonic development in zebrafish may not require the function of the canonical GINS complex as neither zygotic Gins1 nor Gins2 isoforms seem to be present during these stages.
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spelling pubmed-72703452020-06-15 Tissue-Specific Requirement for the GINS Complex During Zebrafish Development Varga, Máté Csályi, Kitti Bertyák, István Menyhárd, Dóra K. Poole, Richard J. Cerveny, Kara L. Kövesdi, Dorottya Barátki, Balázs Rouse, Hannah Vad, Zsuzsa Hawkins, Thomas A. Stickney, Heather L. Cavodeassi, Florencia Schwarz, Quenten Young, Rodrigo M. Wilson, Stephen W. Front Cell Dev Biol Cell and Developmental Biology Efficient and accurate DNA replication is particularly critical in stem and progenitor cells for successful proliferation and survival. The replisome, an amalgam of protein complexes, is responsible for binding potential origins of replication, unwinding the double helix, and then synthesizing complimentary strands of DNA. According to current models, the initial steps of DNA unwinding and opening are facilitated by the CMG complex, which is composed of a GINS heterotetramer that connects Cdc45 with the mini-chromosome maintenance (Mcm) helicase. In this work, we provide evidence that in the absence of GINS function DNA replication is cell autonomously impaired, and we also show that gins1 and gins2 mutants exhibit elevated levels of apoptosis restricted to actively proliferating regions of the central nervous system (CNS). Intriguingly, our results also suggest that the rapid cell cycles during early embryonic development in zebrafish may not require the function of the canonical GINS complex as neither zygotic Gins1 nor Gins2 isoforms seem to be present during these stages. Frontiers Media S.A. 2020-05-28 /pmc/articles/PMC7270345/ /pubmed/32548116 http://dx.doi.org/10.3389/fcell.2020.00373 Text en Copyright © 2020 Varga, Csályi, Bertyák, Menyhárd, Poole, Cerveny, Kövesdi, Barátki, Rouse, Vad, Hawkins, Stickney, Cavodeassi, Schwarz, Young and Wilson. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Varga, Máté
Csályi, Kitti
Bertyák, István
Menyhárd, Dóra K.
Poole, Richard J.
Cerveny, Kara L.
Kövesdi, Dorottya
Barátki, Balázs
Rouse, Hannah
Vad, Zsuzsa
Hawkins, Thomas A.
Stickney, Heather L.
Cavodeassi, Florencia
Schwarz, Quenten
Young, Rodrigo M.
Wilson, Stephen W.
Tissue-Specific Requirement for the GINS Complex During Zebrafish Development
title Tissue-Specific Requirement for the GINS Complex During Zebrafish Development
title_full Tissue-Specific Requirement for the GINS Complex During Zebrafish Development
title_fullStr Tissue-Specific Requirement for the GINS Complex During Zebrafish Development
title_full_unstemmed Tissue-Specific Requirement for the GINS Complex During Zebrafish Development
title_short Tissue-Specific Requirement for the GINS Complex During Zebrafish Development
title_sort tissue-specific requirement for the gins complex during zebrafish development
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7270345/
https://www.ncbi.nlm.nih.gov/pubmed/32548116
http://dx.doi.org/10.3389/fcell.2020.00373
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