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NME proteins regulate class switch recombination
Class switch recombination (CSR) in B cells involves deletion‐recombination at switch (S) region DNA and is important for the diversification of antibody isotypes during an immune response. Here, we identify two NME [NM23/NDPK (nucleoside diphosphate kinase)] isoforms, NME1 and NME2, as novel player...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333498/ https://www.ncbi.nlm.nih.gov/pubmed/30411342 http://dx.doi.org/10.1002/1873-3468.13290 |
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author | Zheng, Simin Kusnadi, Anthony Choi, Jee Eun Vuong, Bao Q. Rhodes, Daniela Chaudhuri, Jayanta |
author_facet | Zheng, Simin Kusnadi, Anthony Choi, Jee Eun Vuong, Bao Q. Rhodes, Daniela Chaudhuri, Jayanta |
author_sort | Zheng, Simin |
collection | PubMed |
description | Class switch recombination (CSR) in B cells involves deletion‐recombination at switch (S) region DNA and is important for the diversification of antibody isotypes during an immune response. Here, we identify two NME [NM23/NDPK (nucleoside diphosphate kinase)] isoforms, NME1 and NME2, as novel players in this process. Knockdown of NME2 leads to decreased CSR, while knockdown of the highly homologous NME1 results in increased CSR. Interestingly, these NME proteins also display differential occupancy at S regions during CSR despite their homology; NME1 binds to S regions prior to stimulation, while NME2 binds to S regions only after stimulation. To the best of our knowledge, this represents the first report of a role for these proteins in the regulation of CSR. |
format | Online Article Text |
id | pubmed-6333498 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63334982019-05-21 NME proteins regulate class switch recombination Zheng, Simin Kusnadi, Anthony Choi, Jee Eun Vuong, Bao Q. Rhodes, Daniela Chaudhuri, Jayanta FEBS Lett Research Letters Class switch recombination (CSR) in B cells involves deletion‐recombination at switch (S) region DNA and is important for the diversification of antibody isotypes during an immune response. Here, we identify two NME [NM23/NDPK (nucleoside diphosphate kinase)] isoforms, NME1 and NME2, as novel players in this process. Knockdown of NME2 leads to decreased CSR, while knockdown of the highly homologous NME1 results in increased CSR. Interestingly, these NME proteins also display differential occupancy at S regions during CSR despite their homology; NME1 binds to S regions prior to stimulation, while NME2 binds to S regions only after stimulation. To the best of our knowledge, this represents the first report of a role for these proteins in the regulation of CSR. John Wiley and Sons Inc. 2018-11-23 2019-01 /pmc/articles/PMC6333498/ /pubmed/30411342 http://dx.doi.org/10.1002/1873-3468.13290 Text en © 2018 The Authors. FEBS Letters published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Letters Zheng, Simin Kusnadi, Anthony Choi, Jee Eun Vuong, Bao Q. Rhodes, Daniela Chaudhuri, Jayanta NME proteins regulate class switch recombination |
title |
NME proteins regulate class switch recombination |
title_full |
NME proteins regulate class switch recombination |
title_fullStr |
NME proteins regulate class switch recombination |
title_full_unstemmed |
NME proteins regulate class switch recombination |
title_short |
NME proteins regulate class switch recombination |
title_sort | nme proteins regulate class switch recombination |
topic | Research Letters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333498/ https://www.ncbi.nlm.nih.gov/pubmed/30411342 http://dx.doi.org/10.1002/1873-3468.13290 |
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