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Duplication of a germline promoter downstream of the IgH 3′ regulatory region impairs class switch recombination

During an adaptive immune response, B cells can change their surface immunoglobulins from IgM to IgG, IgE or IgA through a process called class switch recombination (CSR). Switching is preceded by inducible non-coding germline transcription (GLT) of the selected constant gene(s), which is largely co...

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Autores principales: Santos, Joana M., Braikia, Fatima-Zohra, Oudinet, Chloé, Haddad, Dania, Conte, Caroline, Dauba, Audrey, Khamlichi, Ahmed Amine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003904/
https://www.ncbi.nlm.nih.gov/pubmed/29907762
http://dx.doi.org/10.1038/s41598-018-27448-4
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author Santos, Joana M.
Braikia, Fatima-Zohra
Oudinet, Chloé
Haddad, Dania
Conte, Caroline
Dauba, Audrey
Khamlichi, Ahmed Amine
author_facet Santos, Joana M.
Braikia, Fatima-Zohra
Oudinet, Chloé
Haddad, Dania
Conte, Caroline
Dauba, Audrey
Khamlichi, Ahmed Amine
author_sort Santos, Joana M.
collection PubMed
description During an adaptive immune response, B cells can change their surface immunoglobulins from IgM to IgG, IgE or IgA through a process called class switch recombination (CSR). Switching is preceded by inducible non-coding germline transcription (GLT) of the selected constant gene(s), which is largely controlled by a super-enhancer called the 3′ regulatory region (3′RR). Despite intense efforts, the precise mechanisms that regulate GLT are still elusive. In order to gain additional insights into these mechanisms, we analyzed GLT and CSR in mutant B cells carrying a duplication of the promoter of the α constant gene (Iα) downstream of 3′RR. Duplication of the Iα promoter affected differently GLT and CSR. While for most isotypes a drop in GLT was accompanied by a decrease in CSR, that was not the case for switching to IgA, which diminished despite unchanged GLT. Unexpectedly, there was no obvious effect on GLT and CSR to IgG3. Remarkably, specific stimuli that normally induce switching to IgG2b had contrasting effects in mutant B cells; Iγ2b was now preferentially responsive to the stimulus that induced Iα promoter. We propose that one mechanism underlying the induced 3′RR-mediated activation of GL promoters involves, at least in part, specific transcription factories.
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spelling pubmed-60039042018-06-26 Duplication of a germline promoter downstream of the IgH 3′ regulatory region impairs class switch recombination Santos, Joana M. Braikia, Fatima-Zohra Oudinet, Chloé Haddad, Dania Conte, Caroline Dauba, Audrey Khamlichi, Ahmed Amine Sci Rep Article During an adaptive immune response, B cells can change their surface immunoglobulins from IgM to IgG, IgE or IgA through a process called class switch recombination (CSR). Switching is preceded by inducible non-coding germline transcription (GLT) of the selected constant gene(s), which is largely controlled by a super-enhancer called the 3′ regulatory region (3′RR). Despite intense efforts, the precise mechanisms that regulate GLT are still elusive. In order to gain additional insights into these mechanisms, we analyzed GLT and CSR in mutant B cells carrying a duplication of the promoter of the α constant gene (Iα) downstream of 3′RR. Duplication of the Iα promoter affected differently GLT and CSR. While for most isotypes a drop in GLT was accompanied by a decrease in CSR, that was not the case for switching to IgA, which diminished despite unchanged GLT. Unexpectedly, there was no obvious effect on GLT and CSR to IgG3. Remarkably, specific stimuli that normally induce switching to IgG2b had contrasting effects in mutant B cells; Iγ2b was now preferentially responsive to the stimulus that induced Iα promoter. We propose that one mechanism underlying the induced 3′RR-mediated activation of GL promoters involves, at least in part, specific transcription factories. Nature Publishing Group UK 2018-06-15 /pmc/articles/PMC6003904/ /pubmed/29907762 http://dx.doi.org/10.1038/s41598-018-27448-4 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Santos, Joana M.
Braikia, Fatima-Zohra
Oudinet, Chloé
Haddad, Dania
Conte, Caroline
Dauba, Audrey
Khamlichi, Ahmed Amine
Duplication of a germline promoter downstream of the IgH 3′ regulatory region impairs class switch recombination
title Duplication of a germline promoter downstream of the IgH 3′ regulatory region impairs class switch recombination
title_full Duplication of a germline promoter downstream of the IgH 3′ regulatory region impairs class switch recombination
title_fullStr Duplication of a germline promoter downstream of the IgH 3′ regulatory region impairs class switch recombination
title_full_unstemmed Duplication of a germline promoter downstream of the IgH 3′ regulatory region impairs class switch recombination
title_short Duplication of a germline promoter downstream of the IgH 3′ regulatory region impairs class switch recombination
title_sort duplication of a germline promoter downstream of the igh 3′ regulatory region impairs class switch recombination
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003904/
https://www.ncbi.nlm.nih.gov/pubmed/29907762
http://dx.doi.org/10.1038/s41598-018-27448-4
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