Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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
_version_ 1782325466488635392
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
work_keys_str_mv AT ebertgrit distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT steiningeranne distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT weißmannrobert distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT boldtvivien distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT lindthomsenallan distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT grunejana distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT badeltstefan distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT heßlermelanie distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT peisermatthias distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT hitzlermanuel distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT jensenlarsr distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT mullerines distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT huhao distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT arndtpeterf distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT kussandreasw distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT tebelkatrin distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7
AT ullmannreinhard distributionofsegmentalduplicationsinthecontextofhigherorderchromatinorganisationofhumanchromosome7