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Common Chromosomal Fragile Sites—Conserved Failure Stories

In order to pass on an intact copy of the genome during cell division, complete and faithful DNA replication is crucial. Yet, certain areas of the genome are intrinsically challenging to replicate, which manifests as high local mutation propensity. Such regions include trinucleotide repeat sequences...

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Detalles Bibliográficos
Autores principales: Voutsinos, Vasileios, Munk, Sebastian H. N., Oestergaard, Vibe H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315858/
https://www.ncbi.nlm.nih.gov/pubmed/30486458
http://dx.doi.org/10.3390/genes9120580
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author Voutsinos, Vasileios
Munk, Sebastian H. N.
Oestergaard, Vibe H.
author_facet Voutsinos, Vasileios
Munk, Sebastian H. N.
Oestergaard, Vibe H.
author_sort Voutsinos, Vasileios
collection PubMed
description In order to pass on an intact copy of the genome during cell division, complete and faithful DNA replication is crucial. Yet, certain areas of the genome are intrinsically challenging to replicate, which manifests as high local mutation propensity. Such regions include trinucleotide repeat sequences, common chromosomal fragile sites (CFSs), and early replicating fragile sites (ERFSs). Despite their genomic instability CFSs are conserved, suggesting that they have a biological function. To shed light on the potential function of CFSs, this review summarizes the similarities and differences of the regions that challenge DNA replication with main focus on CFSs. Moreover, we review the mechanisms that operate when CFSs fail to complete replication before entry into mitosis. Finally, evolutionary perspectives and potential physiological roles of CFSs are discussed with emphasis on their potential role in neurogenesis.
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spelling pubmed-63158582019-01-09 Common Chromosomal Fragile Sites—Conserved Failure Stories Voutsinos, Vasileios Munk, Sebastian H. N. Oestergaard, Vibe H. Genes (Basel) Review In order to pass on an intact copy of the genome during cell division, complete and faithful DNA replication is crucial. Yet, certain areas of the genome are intrinsically challenging to replicate, which manifests as high local mutation propensity. Such regions include trinucleotide repeat sequences, common chromosomal fragile sites (CFSs), and early replicating fragile sites (ERFSs). Despite their genomic instability CFSs are conserved, suggesting that they have a biological function. To shed light on the potential function of CFSs, this review summarizes the similarities and differences of the regions that challenge DNA replication with main focus on CFSs. Moreover, we review the mechanisms that operate when CFSs fail to complete replication before entry into mitosis. Finally, evolutionary perspectives and potential physiological roles of CFSs are discussed with emphasis on their potential role in neurogenesis. MDPI 2018-11-27 /pmc/articles/PMC6315858/ /pubmed/30486458 http://dx.doi.org/10.3390/genes9120580 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
Voutsinos, Vasileios
Munk, Sebastian H. N.
Oestergaard, Vibe H.
Common Chromosomal Fragile Sites—Conserved Failure Stories
title Common Chromosomal Fragile Sites—Conserved Failure Stories
title_full Common Chromosomal Fragile Sites—Conserved Failure Stories
title_fullStr Common Chromosomal Fragile Sites—Conserved Failure Stories
title_full_unstemmed Common Chromosomal Fragile Sites—Conserved Failure Stories
title_short Common Chromosomal Fragile Sites—Conserved Failure Stories
title_sort common chromosomal fragile sites—conserved failure stories
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315858/
https://www.ncbi.nlm.nih.gov/pubmed/30486458
http://dx.doi.org/10.3390/genes9120580
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