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The IgH locus 3′ cis-regulatory super-enhancer co-opts AID for allelic transvection
Immunoglobulin heavy chain (IgH) alleles have ambivalent relationships: they feature both allelic exclusion, ensuring monoallelic expression of a single immunoglobulin (Ig) allele, and frequent inter-allelic class-switch recombination (CSR) reassembling genes from both alleles. The IgH locus 3′ regu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355067/ https://www.ncbi.nlm.nih.gov/pubmed/28088785 http://dx.doi.org/10.18632/oncotarget.14585 |
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author | Le Noir, Sandrine Laffleur, Brice Carrion, Claire Garot, Armand Lecardeur, Sandrine Pinaud, Eric Denizot, Yves Skok, Jane Cogné, Michel |
author_facet | Le Noir, Sandrine Laffleur, Brice Carrion, Claire Garot, Armand Lecardeur, Sandrine Pinaud, Eric Denizot, Yves Skok, Jane Cogné, Michel |
author_sort | Le Noir, Sandrine |
collection | PubMed |
description | Immunoglobulin heavy chain (IgH) alleles have ambivalent relationships: they feature both allelic exclusion, ensuring monoallelic expression of a single immunoglobulin (Ig) allele, and frequent inter-allelic class-switch recombination (CSR) reassembling genes from both alleles. The IgH locus 3′ regulatory region (3′RR) includes several transcriptional cis-enhancers promoting activation-induced cytidine deaminase (AID)-dependent somatic hypermutation (SHM) and CSR, and altogether behaves as a strong super-enhancer. It can also promote deregulated expression of translocated oncogenes during lymphomagenesis. Besides these rare, illegitimate and pathogenic interactions, we now show that under physiological conditions, the 3′RR super-enhancer supports not only legitimate cis-, but also trans-recruitment of AID, contributing to IgH inter-allelic proximity and enabling the super-enhancer on one allele to stimulate biallelic SHM and CSR. Such inter-allelic activating interactions define transvection, a phenomenon well-known in drosophila but rarely observed in mammalian cells, now appearing as a unique feature of the IgH 3′RR super-enhancer. |
format | Online Article Text |
id | pubmed-5355067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53550672017-04-15 The IgH locus 3′ cis-regulatory super-enhancer co-opts AID for allelic transvection Le Noir, Sandrine Laffleur, Brice Carrion, Claire Garot, Armand Lecardeur, Sandrine Pinaud, Eric Denizot, Yves Skok, Jane Cogné, Michel Oncotarget Research Paper Immunoglobulin heavy chain (IgH) alleles have ambivalent relationships: they feature both allelic exclusion, ensuring monoallelic expression of a single immunoglobulin (Ig) allele, and frequent inter-allelic class-switch recombination (CSR) reassembling genes from both alleles. The IgH locus 3′ regulatory region (3′RR) includes several transcriptional cis-enhancers promoting activation-induced cytidine deaminase (AID)-dependent somatic hypermutation (SHM) and CSR, and altogether behaves as a strong super-enhancer. It can also promote deregulated expression of translocated oncogenes during lymphomagenesis. Besides these rare, illegitimate and pathogenic interactions, we now show that under physiological conditions, the 3′RR super-enhancer supports not only legitimate cis-, but also trans-recruitment of AID, contributing to IgH inter-allelic proximity and enabling the super-enhancer on one allele to stimulate biallelic SHM and CSR. Such inter-allelic activating interactions define transvection, a phenomenon well-known in drosophila but rarely observed in mammalian cells, now appearing as a unique feature of the IgH 3′RR super-enhancer. Impact Journals LLC 2017-01-10 /pmc/articles/PMC5355067/ /pubmed/28088785 http://dx.doi.org/10.18632/oncotarget.14585 Text en Copyright: © 2017 Le Noir et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Le Noir, Sandrine Laffleur, Brice Carrion, Claire Garot, Armand Lecardeur, Sandrine Pinaud, Eric Denizot, Yves Skok, Jane Cogné, Michel The IgH locus 3′ cis-regulatory super-enhancer co-opts AID for allelic transvection |
title | The IgH locus 3′ cis-regulatory super-enhancer co-opts AID for allelic transvection |
title_full | The IgH locus 3′ cis-regulatory super-enhancer co-opts AID for allelic transvection |
title_fullStr | The IgH locus 3′ cis-regulatory super-enhancer co-opts AID for allelic transvection |
title_full_unstemmed | The IgH locus 3′ cis-regulatory super-enhancer co-opts AID for allelic transvection |
title_short | The IgH locus 3′ cis-regulatory super-enhancer co-opts AID for allelic transvection |
title_sort | igh locus 3′ cis-regulatory super-enhancer co-opts aid for allelic transvection |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355067/ https://www.ncbi.nlm.nih.gov/pubmed/28088785 http://dx.doi.org/10.18632/oncotarget.14585 |
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