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Molecular and Cellular Functions of the Warsaw Breakage Syndrome DNA Helicase DDX11

DDX11/ChlR1 (Chl1 in yeast) is a DNA helicase involved in sister chromatid cohesion and in DNA repair pathways. The protein belongs to the family of the iron–sulphur cluster containing DNA helicases, whose deficiencies have been linked to a number of diseases affecting genome stability. Mutations of...

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Autores principales: Pisani, Francesca M., Napolitano, Ettore, Napolitano, Luisa M. R., Onesti, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6266566/
https://www.ncbi.nlm.nih.gov/pubmed/30469382
http://dx.doi.org/10.3390/genes9110564
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author Pisani, Francesca M.
Napolitano, Ettore
Napolitano, Luisa M. R.
Onesti, Silvia
author_facet Pisani, Francesca M.
Napolitano, Ettore
Napolitano, Luisa M. R.
Onesti, Silvia
author_sort Pisani, Francesca M.
collection PubMed
description DDX11/ChlR1 (Chl1 in yeast) is a DNA helicase involved in sister chromatid cohesion and in DNA repair pathways. The protein belongs to the family of the iron–sulphur cluster containing DNA helicases, whose deficiencies have been linked to a number of diseases affecting genome stability. Mutations of human DDX11 are indeed associated with the rare genetic disorder named Warsaw breakage syndrome, showing both chromosomal breakages and chromatid cohesion defects. Moreover, growing evidence of a potential role in oncogenesis further emphasizes the clinical relevance of DDX11. Here, we illustrate the biochemical and structural features of DDX11 and how it cooperates with multiple protein partners in the cell, acting at the interface of DNA replication/repair/recombination and sister chromatid cohesion to preserve genome stability.
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spelling pubmed-62665662018-12-13 Molecular and Cellular Functions of the Warsaw Breakage Syndrome DNA Helicase DDX11 Pisani, Francesca M. Napolitano, Ettore Napolitano, Luisa M. R. Onesti, Silvia Genes (Basel) Review DDX11/ChlR1 (Chl1 in yeast) is a DNA helicase involved in sister chromatid cohesion and in DNA repair pathways. The protein belongs to the family of the iron–sulphur cluster containing DNA helicases, whose deficiencies have been linked to a number of diseases affecting genome stability. Mutations of human DDX11 are indeed associated with the rare genetic disorder named Warsaw breakage syndrome, showing both chromosomal breakages and chromatid cohesion defects. Moreover, growing evidence of a potential role in oncogenesis further emphasizes the clinical relevance of DDX11. Here, we illustrate the biochemical and structural features of DDX11 and how it cooperates with multiple protein partners in the cell, acting at the interface of DNA replication/repair/recombination and sister chromatid cohesion to preserve genome stability. MDPI 2018-11-21 /pmc/articles/PMC6266566/ /pubmed/30469382 http://dx.doi.org/10.3390/genes9110564 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Pisani, Francesca M.
Napolitano, Ettore
Napolitano, Luisa M. R.
Onesti, Silvia
Molecular and Cellular Functions of the Warsaw Breakage Syndrome DNA Helicase DDX11
title Molecular and Cellular Functions of the Warsaw Breakage Syndrome DNA Helicase DDX11
title_full Molecular and Cellular Functions of the Warsaw Breakage Syndrome DNA Helicase DDX11
title_fullStr Molecular and Cellular Functions of the Warsaw Breakage Syndrome DNA Helicase DDX11
title_full_unstemmed Molecular and Cellular Functions of the Warsaw Breakage Syndrome DNA Helicase DDX11
title_short Molecular and Cellular Functions of the Warsaw Breakage Syndrome DNA Helicase DDX11
title_sort molecular and cellular functions of the warsaw breakage syndrome dna helicase ddx11
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6266566/
https://www.ncbi.nlm.nih.gov/pubmed/30469382
http://dx.doi.org/10.3390/genes9110564
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