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New insights emerge as antibody repertoire diversification meets chromosome conformation

Vast repertoires of unique antigen receptors are created in developing lymphocytes. The antigen receptor loci contain many variable (V), diversity (D), and joining (J) gene segments that are arrayed across very large genomic expanses and are joined to form variable-region exons. This process creates...

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Detalles Bibliográficos
Autores principales: Kenter, Amy L., Feeney, Ann J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439775/
https://www.ncbi.nlm.nih.gov/pubmed/30984378
http://dx.doi.org/10.12688/f1000research.17358.1
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author Kenter, Amy L.
Feeney, Ann J.
author_facet Kenter, Amy L.
Feeney, Ann J.
author_sort Kenter, Amy L.
collection PubMed
description Vast repertoires of unique antigen receptors are created in developing lymphocytes. The antigen receptor loci contain many variable (V), diversity (D), and joining (J) gene segments that are arrayed across very large genomic expanses and are joined to form variable-region exons. This process creates the potential for an organism to respond to large numbers of different pathogens. Here, we consider the underlying molecular mechanisms that favor some V genes for recombination prior to selection of the final antigen receptor repertoire. We discuss chromatin structures that form in antigen receptor loci to permit spatial proximity among the V, D, and J gene segments and how these relate to the generation of antigen receptor diversity.
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spelling pubmed-64397752019-04-12 New insights emerge as antibody repertoire diversification meets chromosome conformation Kenter, Amy L. Feeney, Ann J. F1000Res Review Vast repertoires of unique antigen receptors are created in developing lymphocytes. The antigen receptor loci contain many variable (V), diversity (D), and joining (J) gene segments that are arrayed across very large genomic expanses and are joined to form variable-region exons. This process creates the potential for an organism to respond to large numbers of different pathogens. Here, we consider the underlying molecular mechanisms that favor some V genes for recombination prior to selection of the final antigen receptor repertoire. We discuss chromatin structures that form in antigen receptor loci to permit spatial proximity among the V, D, and J gene segments and how these relate to the generation of antigen receptor diversity. F1000 Research Limited 2019-03-28 /pmc/articles/PMC6439775/ /pubmed/30984378 http://dx.doi.org/10.12688/f1000research.17358.1 Text en Copyright: © 2019 Kenter AL and Feeney AJ http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Kenter, Amy L.
Feeney, Ann J.
New insights emerge as antibody repertoire diversification meets chromosome conformation
title New insights emerge as antibody repertoire diversification meets chromosome conformation
title_full New insights emerge as antibody repertoire diversification meets chromosome conformation
title_fullStr New insights emerge as antibody repertoire diversification meets chromosome conformation
title_full_unstemmed New insights emerge as antibody repertoire diversification meets chromosome conformation
title_short New insights emerge as antibody repertoire diversification meets chromosome conformation
title_sort new insights emerge as antibody repertoire diversification meets chromosome conformation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439775/
https://www.ncbi.nlm.nih.gov/pubmed/30984378
http://dx.doi.org/10.12688/f1000research.17358.1
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