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Genomic regions with distinct genomic distance conservation in vertebrate genomes

BACKGROUND: A number of vertebrate highly conserved elements (HCEs) have been detected and their genomic interval distances have been reported to be more conserved than protein coding genes among mammalian genomes. A characteristic of the human – non-mammalian comparisons is a bimodal distribution o...

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Autores principales: Sun, Hong, Skogerbø, Geir, Zheng, Xiaohui, Liu, Wei, Li, Yixue
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667192/
https://www.ncbi.nlm.nih.gov/pubmed/19323843
http://dx.doi.org/10.1186/1471-2164-10-133
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author Sun, Hong
Skogerbø, Geir
Zheng, Xiaohui
Liu, Wei
Li, Yixue
author_facet Sun, Hong
Skogerbø, Geir
Zheng, Xiaohui
Liu, Wei
Li, Yixue
author_sort Sun, Hong
collection PubMed
description BACKGROUND: A number of vertebrate highly conserved elements (HCEs) have been detected and their genomic interval distances have been reported to be more conserved than protein coding genes among mammalian genomes. A characteristic of the human – non-mammalian comparisons is a bimodal distribution of relative distance difference of conserved consecutive HCE pairs; and it is difficult to attribute such profile to a random assortment. We therefore undertook an analysis of the human genomic regions confined by consecutive HCE pairs common to eight genomes (human, mouse, rat, chicken, frog, zebrafish, tetradon and fugu). RESULTS: Among HCE pairs, we found that some consistently preserve highly conserved interval distance among genomes while others have relatively low distance conservation. Using a partition method, we detected two groups of inter-HCE regions (IHRs) with distinct distance conservation pattern in vertebrate genomes: IHR1s that are bordered by HCE pairs with relative small distance variation, and IHR2s with larger distance difference values. Compared to random background, annotated repeat sequences are significantly less frequent in IHR1s than IHR2s, which reflects a correlation between repeat sequences and the length expansion of IHRs. Both groups of IHRs are unexpectedly enriched in human indel (i.e. insertion and deletion) polymorphism-variations than random background. The correlation between the percentage of conserved sequence and human IHR length was stronger for IHR1 than IHR2. Both groups of IHRs are significantly enriched for CpG islands. CONCLUSION: The data suggest that subsets of HCE pairs may undergo different evolutionary paths in light of their genomic distance conservation, and that sets of genomic regions pertain to HCEs, as well as the region in which HCEs reside, should be treated as integrated domains.
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spelling pubmed-26671922009-04-09 Genomic regions with distinct genomic distance conservation in vertebrate genomes Sun, Hong Skogerbø, Geir Zheng, Xiaohui Liu, Wei Li, Yixue BMC Genomics Research Article BACKGROUND: A number of vertebrate highly conserved elements (HCEs) have been detected and their genomic interval distances have been reported to be more conserved than protein coding genes among mammalian genomes. A characteristic of the human – non-mammalian comparisons is a bimodal distribution of relative distance difference of conserved consecutive HCE pairs; and it is difficult to attribute such profile to a random assortment. We therefore undertook an analysis of the human genomic regions confined by consecutive HCE pairs common to eight genomes (human, mouse, rat, chicken, frog, zebrafish, tetradon and fugu). RESULTS: Among HCE pairs, we found that some consistently preserve highly conserved interval distance among genomes while others have relatively low distance conservation. Using a partition method, we detected two groups of inter-HCE regions (IHRs) with distinct distance conservation pattern in vertebrate genomes: IHR1s that are bordered by HCE pairs with relative small distance variation, and IHR2s with larger distance difference values. Compared to random background, annotated repeat sequences are significantly less frequent in IHR1s than IHR2s, which reflects a correlation between repeat sequences and the length expansion of IHRs. Both groups of IHRs are unexpectedly enriched in human indel (i.e. insertion and deletion) polymorphism-variations than random background. The correlation between the percentage of conserved sequence and human IHR length was stronger for IHR1 than IHR2. Both groups of IHRs are significantly enriched for CpG islands. CONCLUSION: The data suggest that subsets of HCE pairs may undergo different evolutionary paths in light of their genomic distance conservation, and that sets of genomic regions pertain to HCEs, as well as the region in which HCEs reside, should be treated as integrated domains. BioMed Central 2009-03-27 /pmc/articles/PMC2667192/ /pubmed/19323843 http://dx.doi.org/10.1186/1471-2164-10-133 Text en Copyright © 2009 Sun et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 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 cited.
spellingShingle Research Article
Sun, Hong
Skogerbø, Geir
Zheng, Xiaohui
Liu, Wei
Li, Yixue
Genomic regions with distinct genomic distance conservation in vertebrate genomes
title Genomic regions with distinct genomic distance conservation in vertebrate genomes
title_full Genomic regions with distinct genomic distance conservation in vertebrate genomes
title_fullStr Genomic regions with distinct genomic distance conservation in vertebrate genomes
title_full_unstemmed Genomic regions with distinct genomic distance conservation in vertebrate genomes
title_short Genomic regions with distinct genomic distance conservation in vertebrate genomes
title_sort genomic regions with distinct genomic distance conservation in vertebrate genomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667192/
https://www.ncbi.nlm.nih.gov/pubmed/19323843
http://dx.doi.org/10.1186/1471-2164-10-133
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