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Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7
BACKGROUND: Segmental duplications (SDs) are not evenly distributed along chromosomes. The reasons for this biased susceptibility to SD insertion are poorly understood. Accumulation of SDs is associated with increased genomic instability, which can lead to structural variants and genomic disorders s...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4092221/ https://www.ncbi.nlm.nih.gov/pubmed/24973960 http://dx.doi.org/10.1186/1471-2164-15-537 |
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author | Ebert, Grit Steininger, Anne Weißmann, Robert Boldt, Vivien Lind-Thomsen, Allan Grune, Jana Badelt, Stefan Heßler, Melanie Peiser, Matthias Hitzler, Manuel Jensen, Lars R Müller, Ines Hu, Hao Arndt, Peter F Kuss, Andreas W Tebel, Katrin Ullmann, Reinhard |
author_facet | Ebert, Grit Steininger, Anne Weißmann, Robert Boldt, Vivien Lind-Thomsen, Allan Grune, Jana Badelt, Stefan Heßler, Melanie Peiser, Matthias Hitzler, Manuel Jensen, Lars R Müller, Ines Hu, Hao Arndt, Peter F Kuss, Andreas W Tebel, Katrin Ullmann, Reinhard |
author_sort | Ebert, Grit |
collection | PubMed |
description | BACKGROUND: Segmental duplications (SDs) are not evenly distributed along chromosomes. The reasons for this biased susceptibility to SD insertion are poorly understood. Accumulation of SDs is associated with increased genomic instability, which can lead to structural variants and genomic disorders such as the Williams-Beuren syndrome. Despite these adverse effects, SDs have become fixed in the human genome. Focusing on chromosome 7, which is particularly rich in interstitial SDs, we have investigated the distribution of SDs in the context of evolution and the three dimensional organisation of the chromosome in order to gain insights into the mutual relationship of SDs and chromatin topology. RESULTS: Intrachromosomal SDs preferentially accumulate in those segments of chromosome 7 that are homologous to marmoset chromosome 2. Although this formerly compact segment has been re-distributed to three different sites during primate evolution, we can show by means of public data on long distance chromatin interactions that these three intervals, and consequently the paralogous SDs mapping to them, have retained their spatial proximity in the nucleus. Focusing on SD clusters implicated in the aetiology of the Williams-Beuren syndrome locus we demonstrate by cross-species comparison that these SDs have inserted at the borders of a topological domain and that they flank regions with distinct DNA conformation. CONCLUSIONS: Our study suggests a link of nuclear architecture and the propagation of SDs across chromosome 7, either by promoting regional SD insertion or by contributing to the establishment of higher order chromatin organisation themselves. The latter could compensate for the high risk of structural rearrangements and thus may have contributed to their evolutionary fixation in the human genome. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-537) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4092221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40922212014-07-21 Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7 Ebert, Grit Steininger, Anne Weißmann, Robert Boldt, Vivien Lind-Thomsen, Allan Grune, Jana Badelt, Stefan Heßler, Melanie Peiser, Matthias Hitzler, Manuel Jensen, Lars R Müller, Ines Hu, Hao Arndt, Peter F Kuss, Andreas W Tebel, Katrin Ullmann, Reinhard BMC Genomics Research Article BACKGROUND: Segmental duplications (SDs) are not evenly distributed along chromosomes. The reasons for this biased susceptibility to SD insertion are poorly understood. Accumulation of SDs is associated with increased genomic instability, which can lead to structural variants and genomic disorders such as the Williams-Beuren syndrome. Despite these adverse effects, SDs have become fixed in the human genome. Focusing on chromosome 7, which is particularly rich in interstitial SDs, we have investigated the distribution of SDs in the context of evolution and the three dimensional organisation of the chromosome in order to gain insights into the mutual relationship of SDs and chromatin topology. RESULTS: Intrachromosomal SDs preferentially accumulate in those segments of chromosome 7 that are homologous to marmoset chromosome 2. Although this formerly compact segment has been re-distributed to three different sites during primate evolution, we can show by means of public data on long distance chromatin interactions that these three intervals, and consequently the paralogous SDs mapping to them, have retained their spatial proximity in the nucleus. Focusing on SD clusters implicated in the aetiology of the Williams-Beuren syndrome locus we demonstrate by cross-species comparison that these SDs have inserted at the borders of a topological domain and that they flank regions with distinct DNA conformation. CONCLUSIONS: Our study suggests a link of nuclear architecture and the propagation of SDs across chromosome 7, either by promoting regional SD insertion or by contributing to the establishment of higher order chromatin organisation themselves. The latter could compensate for the high risk of structural rearrangements and thus may have contributed to their evolutionary fixation in the human genome. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-537) contains supplementary material, which is available to authorized users. BioMed Central 2014-06-29 /pmc/articles/PMC4092221/ /pubmed/24973960 http://dx.doi.org/10.1186/1471-2164-15-537 Text en © Ebert et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Ebert, Grit Steininger, Anne Weißmann, Robert Boldt, Vivien Lind-Thomsen, Allan Grune, Jana Badelt, Stefan Heßler, Melanie Peiser, Matthias Hitzler, Manuel Jensen, Lars R Müller, Ines Hu, Hao Arndt, Peter F Kuss, Andreas W Tebel, Katrin Ullmann, Reinhard Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7 |
title | Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7 |
title_full | Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7 |
title_fullStr | Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7 |
title_full_unstemmed | Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7 |
title_short | Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7 |
title_sort | distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4092221/ https://www.ncbi.nlm.nih.gov/pubmed/24973960 http://dx.doi.org/10.1186/1471-2164-15-537 |
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