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Loop extrusion promotes an alternate pathway for isotype switching

Class-switch recombination (CSR) involves replacement of the Cμ constant region with another downstream C(H) region. CSR is initiated by activation-induced cytidine deaminase (AID)-mediated DNA breaks that are targeted to transcriptionally active switch (S) regions. S region promoters (Prs) direct s...

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Autores principales: Shen, Hong Ming, Wuerffel, Robert, Cantillo, Jose F., Priyadarshi, Saurabh, Lei, Xue, Liang, Jie, Wu, Yee Ling, Kenter, Amy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8979556/
https://www.ncbi.nlm.nih.gov/pubmed/34818547
http://dx.doi.org/10.1016/j.celrep.2021.110059
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author Shen, Hong Ming
Wuerffel, Robert
Cantillo, Jose F.
Priyadarshi, Saurabh
Lei, Xue
Liang, Jie
Wu, Yee Ling
Kenter, Amy L.
author_facet Shen, Hong Ming
Wuerffel, Robert
Cantillo, Jose F.
Priyadarshi, Saurabh
Lei, Xue
Liang, Jie
Wu, Yee Ling
Kenter, Amy L.
author_sort Shen, Hong Ming
collection PubMed
description Class-switch recombination (CSR) involves replacement of the Cμ constant region with another downstream C(H) region. CSR is initiated by activation-induced cytidine deaminase (AID)-mediated DNA breaks that are targeted to transcriptionally active switch (S) regions. S region promoters (Prs) direct synapsis by associating with the Eμ and 3′Eα enhancers that jointly anchor a chromatin loop. We report that asymmetric loop extrusion allows 3′Eα to track along the locus and form Pr-Pr-E interactions that mediate CSR between downstream S regions, followed by switching to donor Sμ. This alternative pathway bypasses sequential switching and creates immunoglobulin (Ig)E(+) B cells in the absence of IgG1 expression. Based on the analysis of diagnostic CSR products in B cell subsets, we identify a BCR-negative cell intermediate that is pivotal to efficient CSR.
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spelling pubmed-89795562022-04-04 Loop extrusion promotes an alternate pathway for isotype switching Shen, Hong Ming Wuerffel, Robert Cantillo, Jose F. Priyadarshi, Saurabh Lei, Xue Liang, Jie Wu, Yee Ling Kenter, Amy L. Cell Rep Article Class-switch recombination (CSR) involves replacement of the Cμ constant region with another downstream C(H) region. CSR is initiated by activation-induced cytidine deaminase (AID)-mediated DNA breaks that are targeted to transcriptionally active switch (S) regions. S region promoters (Prs) direct synapsis by associating with the Eμ and 3′Eα enhancers that jointly anchor a chromatin loop. We report that asymmetric loop extrusion allows 3′Eα to track along the locus and form Pr-Pr-E interactions that mediate CSR between downstream S regions, followed by switching to donor Sμ. This alternative pathway bypasses sequential switching and creates immunoglobulin (Ig)E(+) B cells in the absence of IgG1 expression. Based on the analysis of diagnostic CSR products in B cell subsets, we identify a BCR-negative cell intermediate that is pivotal to efficient CSR. 2021-11-23 /pmc/articles/PMC8979556/ /pubmed/34818547 http://dx.doi.org/10.1016/j.celrep.2021.110059 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Shen, Hong Ming
Wuerffel, Robert
Cantillo, Jose F.
Priyadarshi, Saurabh
Lei, Xue
Liang, Jie
Wu, Yee Ling
Kenter, Amy L.
Loop extrusion promotes an alternate pathway for isotype switching
title Loop extrusion promotes an alternate pathway for isotype switching
title_full Loop extrusion promotes an alternate pathway for isotype switching
title_fullStr Loop extrusion promotes an alternate pathway for isotype switching
title_full_unstemmed Loop extrusion promotes an alternate pathway for isotype switching
title_short Loop extrusion promotes an alternate pathway for isotype switching
title_sort loop extrusion promotes an alternate pathway for isotype switching
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8979556/
https://www.ncbi.nlm.nih.gov/pubmed/34818547
http://dx.doi.org/10.1016/j.celrep.2021.110059
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