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Short tandem repeats, segmental duplications, gene deletion, and genomic instability in a rapidly diversified immune gene family

BACKGROUND: Genomic regions with repetitive sequences are considered unstable and prone to swift DNA diversification processes. A highly diverse immune gene family of the sea urchin (Strongylocentrotus purpuratus), called Sp185/333, is composed of clustered genes with similar sequence as well as sev...

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Autores principales: Oren, Matan, Barela Hudgell, Megan A., D’Allura, Brian, Agronin, Jacob, Gross, Alexandra, Podini, Daniele, Smith, L. Courtney
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5103432/
https://www.ncbi.nlm.nih.gov/pubmed/27829352
http://dx.doi.org/10.1186/s12864-016-3241-x
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author Oren, Matan
Barela Hudgell, Megan A.
D’Allura, Brian
Agronin, Jacob
Gross, Alexandra
Podini, Daniele
Smith, L. Courtney
author_facet Oren, Matan
Barela Hudgell, Megan A.
D’Allura, Brian
Agronin, Jacob
Gross, Alexandra
Podini, Daniele
Smith, L. Courtney
author_sort Oren, Matan
collection PubMed
description BACKGROUND: Genomic regions with repetitive sequences are considered unstable and prone to swift DNA diversification processes. A highly diverse immune gene family of the sea urchin (Strongylocentrotus purpuratus), called Sp185/333, is composed of clustered genes with similar sequence as well as several types of repeats ranging in size from short tandem repeats (STRs) to large segmental duplications. This repetitive structure may have been the basis for the incorrect assembly of this gene family in the sea urchin genome sequence. Consequently, we have resolved the structure of the family and profiled the members by sequencing selected BAC clones using Illumina and PacBio approaches. RESULTS: BAC insert assemblies identified 15 predicted genes that are organized into three clusters. Two of the gene clusters have almost identical flanking regions, suggesting that they may be non-matching allelic clusters residing at the same genomic locus. GA STRs surround all genes and appear in large stretches at locations of putatively deleted genes. GAT STRs are positioned at the edges of segmental duplications that include a subset of the genes. The unique locations of the STRs suggest their involvement in gene deletions and segmental duplications. Genomic profiling of the Sp185/333 gene diversity in 10 sea urchins shows that no gene repertoires are shared among individuals indicating a very high gene diversification rate for this family. CONCLUSIONS: The repetitive genomic structure of the Sp185/333 family that includes STRs in strategic locations may serve as platform for a controlled mechanism which regulates the processes of gene recombination, gene conversion, duplication and deletion. The outcome is genomic instability and allelic mismatches, which may further drive the swift diversification of the Sp185/333 gene family that may improve the immune fitness of the species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3241-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-51034322016-11-10 Short tandem repeats, segmental duplications, gene deletion, and genomic instability in a rapidly diversified immune gene family Oren, Matan Barela Hudgell, Megan A. D’Allura, Brian Agronin, Jacob Gross, Alexandra Podini, Daniele Smith, L. Courtney BMC Genomics Research Article BACKGROUND: Genomic regions with repetitive sequences are considered unstable and prone to swift DNA diversification processes. A highly diverse immune gene family of the sea urchin (Strongylocentrotus purpuratus), called Sp185/333, is composed of clustered genes with similar sequence as well as several types of repeats ranging in size from short tandem repeats (STRs) to large segmental duplications. This repetitive structure may have been the basis for the incorrect assembly of this gene family in the sea urchin genome sequence. Consequently, we have resolved the structure of the family and profiled the members by sequencing selected BAC clones using Illumina and PacBio approaches. RESULTS: BAC insert assemblies identified 15 predicted genes that are organized into three clusters. Two of the gene clusters have almost identical flanking regions, suggesting that they may be non-matching allelic clusters residing at the same genomic locus. GA STRs surround all genes and appear in large stretches at locations of putatively deleted genes. GAT STRs are positioned at the edges of segmental duplications that include a subset of the genes. The unique locations of the STRs suggest their involvement in gene deletions and segmental duplications. Genomic profiling of the Sp185/333 gene diversity in 10 sea urchins shows that no gene repertoires are shared among individuals indicating a very high gene diversification rate for this family. CONCLUSIONS: The repetitive genomic structure of the Sp185/333 family that includes STRs in strategic locations may serve as platform for a controlled mechanism which regulates the processes of gene recombination, gene conversion, duplication and deletion. The outcome is genomic instability and allelic mismatches, which may further drive the swift diversification of the Sp185/333 gene family that may improve the immune fitness of the species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3241-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-09 /pmc/articles/PMC5103432/ /pubmed/27829352 http://dx.doi.org/10.1186/s12864-016-3241-x Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Oren, Matan
Barela Hudgell, Megan A.
D’Allura, Brian
Agronin, Jacob
Gross, Alexandra
Podini, Daniele
Smith, L. Courtney
Short tandem repeats, segmental duplications, gene deletion, and genomic instability in a rapidly diversified immune gene family
title Short tandem repeats, segmental duplications, gene deletion, and genomic instability in a rapidly diversified immune gene family
title_full Short tandem repeats, segmental duplications, gene deletion, and genomic instability in a rapidly diversified immune gene family
title_fullStr Short tandem repeats, segmental duplications, gene deletion, and genomic instability in a rapidly diversified immune gene family
title_full_unstemmed Short tandem repeats, segmental duplications, gene deletion, and genomic instability in a rapidly diversified immune gene family
title_short Short tandem repeats, segmental duplications, gene deletion, and genomic instability in a rapidly diversified immune gene family
title_sort short tandem repeats, segmental duplications, gene deletion, and genomic instability in a rapidly diversified immune gene family
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5103432/
https://www.ncbi.nlm.nih.gov/pubmed/27829352
http://dx.doi.org/10.1186/s12864-016-3241-x
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