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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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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. |
format | Online Article Text |
id | pubmed-6315858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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