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ALTernative Functions for Human FANCM at Telomeres

The human FANCM ATPase/translocase is involved in various cellular pathways including DNA damage repair, replication fork remodeling and R-loop resolution. Recently, reports from three independent laboratories have disclosed a previously unappreciated role for FANCM in telomerase-negative human canc...

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Autores principales: Domingues-Silva, Beatriz, Silva, Bruno, Azzalin, Claus M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6743340/
https://www.ncbi.nlm.nih.gov/pubmed/31552268
http://dx.doi.org/10.3389/fmolb.2019.00084
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author Domingues-Silva, Beatriz
Silva, Bruno
Azzalin, Claus M.
author_facet Domingues-Silva, Beatriz
Silva, Bruno
Azzalin, Claus M.
author_sort Domingues-Silva, Beatriz
collection PubMed
description The human FANCM ATPase/translocase is involved in various cellular pathways including DNA damage repair, replication fork remodeling and R-loop resolution. Recently, reports from three independent laboratories have disclosed a previously unappreciated role for FANCM in telomerase-negative human cancer cells that maintain their telomeres through the Alternative Lengthening of Telomeres (ALT) pathway. In ALT cells, FANCM limits telomeric replication stress and damage, and, in turn, ALT activity by suppressing accumulation of telomeric R-loops and by regulating the action of the BLM helicase. As a consequence, FANCM inactivation leads to exaggerated ALT activity and ultimately cell death. The studies reviewed here not only unveil a novel function for human FANCM, but also point to this enzyme as a promising target for anti-ALT cancer therapy.
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spelling pubmed-67433402019-09-24 ALTernative Functions for Human FANCM at Telomeres Domingues-Silva, Beatriz Silva, Bruno Azzalin, Claus M. Front Mol Biosci Molecular Biosciences The human FANCM ATPase/translocase is involved in various cellular pathways including DNA damage repair, replication fork remodeling and R-loop resolution. Recently, reports from three independent laboratories have disclosed a previously unappreciated role for FANCM in telomerase-negative human cancer cells that maintain their telomeres through the Alternative Lengthening of Telomeres (ALT) pathway. In ALT cells, FANCM limits telomeric replication stress and damage, and, in turn, ALT activity by suppressing accumulation of telomeric R-loops and by regulating the action of the BLM helicase. As a consequence, FANCM inactivation leads to exaggerated ALT activity and ultimately cell death. The studies reviewed here not only unveil a novel function for human FANCM, but also point to this enzyme as a promising target for anti-ALT cancer therapy. Frontiers Media S.A. 2019-09-06 /pmc/articles/PMC6743340/ /pubmed/31552268 http://dx.doi.org/10.3389/fmolb.2019.00084 Text en Copyright © 2019 Domingues-Silva, Silva and Azzalin. 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 Molecular Biosciences
Domingues-Silva, Beatriz
Silva, Bruno
Azzalin, Claus M.
ALTernative Functions for Human FANCM at Telomeres
title ALTernative Functions for Human FANCM at Telomeres
title_full ALTernative Functions for Human FANCM at Telomeres
title_fullStr ALTernative Functions for Human FANCM at Telomeres
title_full_unstemmed ALTernative Functions for Human FANCM at Telomeres
title_short ALTernative Functions for Human FANCM at Telomeres
title_sort alternative functions for human fancm at telomeres
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6743340/
https://www.ncbi.nlm.nih.gov/pubmed/31552268
http://dx.doi.org/10.3389/fmolb.2019.00084
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