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Human subtelomeric duplicon structure and organization

BACKGROUND: Human subtelomeric segmental duplications ('subtelomeric repeats') comprise about 25% of the most distal 500 kb and 80% of the most distal 100 kb in human DNA. A systematic analysis of the duplication substructure of human subtelomeric regions was done in order to develop a det...

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Autores principales: Ambrosini, Anthony, Paul, Sheila, Hu, Sufen, Riethman, Harold
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2323237/
https://www.ncbi.nlm.nih.gov/pubmed/17663781
http://dx.doi.org/10.1186/gb-2007-8-7-r151
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author Ambrosini, Anthony
Paul, Sheila
Hu, Sufen
Riethman, Harold
author_facet Ambrosini, Anthony
Paul, Sheila
Hu, Sufen
Riethman, Harold
author_sort Ambrosini, Anthony
collection PubMed
description BACKGROUND: Human subtelomeric segmental duplications ('subtelomeric repeats') comprise about 25% of the most distal 500 kb and 80% of the most distal 100 kb in human DNA. A systematic analysis of the duplication substructure of human subtelomeric regions was done in order to develop a detailed understanding of subtelomeric sequence organization and a nucleotide sequence-level characterization of subtelomeric duplicon families. RESULTS: The extent of nucleotide sequence divergence within subtelomeric duplicon families varies considerably, as does the organization of duplicon blocks at subtelomere alleles. Subtelomeric internal (TTAGGG)n-like tracts occur at duplicon boundaries, suggesting their involvement in the generation of the complex sequence organization. Most duplicons have copies at both subtelomere and non-subtelomere locations, but a class of duplicon blocks is identified that are subtelomere-specific. In addition, a group of six subterminal duplicon families are identified that, together with six single-copy telomere-adjacent segments, include all of the (TTAGGG)n-adjacent sequence identified so far in the human genome. CONCLUSION: Identification of a class of duplicon blocks that is subtelomere-specific will facilitate high-resolution analysis of subtelomere repeat copy number variation as well as studies involving somatic subtelomere rearrangements. The significant levels of nucleotide sequence divergence within many duplicon families as well as the differential organization of duplicon blocks on subtelomere alleles may provide opportunities for allele-specific subtelomere marker development; this is especially true for subterminal regions, where divergence and organizational differences are the greatest. These subterminal sequence families comprise the immediate cis-elements for (TTAGGG)n tracts, and are prime candidates for subtelomeric sequences regulating telomere-specific (TTAGGG)n tract length in humans.
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spelling pubmed-23232372008-04-19 Human subtelomeric duplicon structure and organization Ambrosini, Anthony Paul, Sheila Hu, Sufen Riethman, Harold Genome Biol Research BACKGROUND: Human subtelomeric segmental duplications ('subtelomeric repeats') comprise about 25% of the most distal 500 kb and 80% of the most distal 100 kb in human DNA. A systematic analysis of the duplication substructure of human subtelomeric regions was done in order to develop a detailed understanding of subtelomeric sequence organization and a nucleotide sequence-level characterization of subtelomeric duplicon families. RESULTS: The extent of nucleotide sequence divergence within subtelomeric duplicon families varies considerably, as does the organization of duplicon blocks at subtelomere alleles. Subtelomeric internal (TTAGGG)n-like tracts occur at duplicon boundaries, suggesting their involvement in the generation of the complex sequence organization. Most duplicons have copies at both subtelomere and non-subtelomere locations, but a class of duplicon blocks is identified that are subtelomere-specific. In addition, a group of six subterminal duplicon families are identified that, together with six single-copy telomere-adjacent segments, include all of the (TTAGGG)n-adjacent sequence identified so far in the human genome. CONCLUSION: Identification of a class of duplicon blocks that is subtelomere-specific will facilitate high-resolution analysis of subtelomere repeat copy number variation as well as studies involving somatic subtelomere rearrangements. The significant levels of nucleotide sequence divergence within many duplicon families as well as the differential organization of duplicon blocks on subtelomere alleles may provide opportunities for allele-specific subtelomere marker development; this is especially true for subterminal regions, where divergence and organizational differences are the greatest. These subterminal sequence families comprise the immediate cis-elements for (TTAGGG)n tracts, and are prime candidates for subtelomeric sequences regulating telomere-specific (TTAGGG)n tract length in humans. BioMed Central 2007 2007-07-30 /pmc/articles/PMC2323237/ /pubmed/17663781 http://dx.doi.org/10.1186/gb-2007-8-7-r151 Text en Copyright © 2007 Ambrosini 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
Ambrosini, Anthony
Paul, Sheila
Hu, Sufen
Riethman, Harold
Human subtelomeric duplicon structure and organization
title Human subtelomeric duplicon structure and organization
title_full Human subtelomeric duplicon structure and organization
title_fullStr Human subtelomeric duplicon structure and organization
title_full_unstemmed Human subtelomeric duplicon structure and organization
title_short Human subtelomeric duplicon structure and organization
title_sort human subtelomeric duplicon structure and organization
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2323237/
https://www.ncbi.nlm.nih.gov/pubmed/17663781
http://dx.doi.org/10.1186/gb-2007-8-7-r151
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