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Immunoglobulin expression and the humoral immune response is regulated by the non-canonical poly(A) polymerase TENT5C

TENT5C is a non-canonical cytoplasmic poly(A) polymerase highly expressed by activated B cells to suppress their proliferation. Here we measure the global distribution of poly(A) tail lengths in responsive B cells using a Nanopore direct RNA-sequencing approach, showing that TENT5C polyadenylates im...

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Autores principales: Bilska, Aleksandra, Kusio-Kobiałka, Monika, Krawczyk, Paweł S., Gewartowska, Olga, Tarkowski, Bartosz, Kobyłecki, Kamil, Nowis, Dominika, Golab, Jakub, Gruchota, Jakub, Borsuk, Ewa, Dziembowski, Andrzej, Mroczek, Seweryn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184606/
https://www.ncbi.nlm.nih.gov/pubmed/32341344
http://dx.doi.org/10.1038/s41467-020-15835-3
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author Bilska, Aleksandra
Kusio-Kobiałka, Monika
Krawczyk, Paweł S.
Gewartowska, Olga
Tarkowski, Bartosz
Kobyłecki, Kamil
Nowis, Dominika
Golab, Jakub
Gruchota, Jakub
Borsuk, Ewa
Dziembowski, Andrzej
Mroczek, Seweryn
author_facet Bilska, Aleksandra
Kusio-Kobiałka, Monika
Krawczyk, Paweł S.
Gewartowska, Olga
Tarkowski, Bartosz
Kobyłecki, Kamil
Nowis, Dominika
Golab, Jakub
Gruchota, Jakub
Borsuk, Ewa
Dziembowski, Andrzej
Mroczek, Seweryn
author_sort Bilska, Aleksandra
collection PubMed
description TENT5C is a non-canonical cytoplasmic poly(A) polymerase highly expressed by activated B cells to suppress their proliferation. Here we measure the global distribution of poly(A) tail lengths in responsive B cells using a Nanopore direct RNA-sequencing approach, showing that TENT5C polyadenylates immunoglobulin mRNAs regulating their half-life and consequently steady-state levels. TENT5C is upregulated in differentiating plasma cells by innate signaling. Compared with wild-type, Tent5c(−/−) mice produce fewer antibodies and have diminished T-cell-independent immune response despite having more CD138(high) plasma cells as a consequence of accelerated differentiation. B cells from Tent5c(−/−) mice also have impaired capacity of the secretory pathway, with reduced ER volume and unfolded protein response. Importantly, these functions of TENT5C are dependent on its enzymatic activity as catalytic mutation knock-in mice display the same defect as Tent5c(−/−). These findings define the role of the TENT5C enzyme in the humoral immune response.
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spelling pubmed-71846062020-04-30 Immunoglobulin expression and the humoral immune response is regulated by the non-canonical poly(A) polymerase TENT5C Bilska, Aleksandra Kusio-Kobiałka, Monika Krawczyk, Paweł S. Gewartowska, Olga Tarkowski, Bartosz Kobyłecki, Kamil Nowis, Dominika Golab, Jakub Gruchota, Jakub Borsuk, Ewa Dziembowski, Andrzej Mroczek, Seweryn Nat Commun Article TENT5C is a non-canonical cytoplasmic poly(A) polymerase highly expressed by activated B cells to suppress their proliferation. Here we measure the global distribution of poly(A) tail lengths in responsive B cells using a Nanopore direct RNA-sequencing approach, showing that TENT5C polyadenylates immunoglobulin mRNAs regulating their half-life and consequently steady-state levels. TENT5C is upregulated in differentiating plasma cells by innate signaling. Compared with wild-type, Tent5c(−/−) mice produce fewer antibodies and have diminished T-cell-independent immune response despite having more CD138(high) plasma cells as a consequence of accelerated differentiation. B cells from Tent5c(−/−) mice also have impaired capacity of the secretory pathway, with reduced ER volume and unfolded protein response. Importantly, these functions of TENT5C are dependent on its enzymatic activity as catalytic mutation knock-in mice display the same defect as Tent5c(−/−). These findings define the role of the TENT5C enzyme in the humoral immune response. Nature Publishing Group UK 2020-04-27 /pmc/articles/PMC7184606/ /pubmed/32341344 http://dx.doi.org/10.1038/s41467-020-15835-3 Text en © The Author(s) 2020 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
Bilska, Aleksandra
Kusio-Kobiałka, Monika
Krawczyk, Paweł S.
Gewartowska, Olga
Tarkowski, Bartosz
Kobyłecki, Kamil
Nowis, Dominika
Golab, Jakub
Gruchota, Jakub
Borsuk, Ewa
Dziembowski, Andrzej
Mroczek, Seweryn
Immunoglobulin expression and the humoral immune response is regulated by the non-canonical poly(A) polymerase TENT5C
title Immunoglobulin expression and the humoral immune response is regulated by the non-canonical poly(A) polymerase TENT5C
title_full Immunoglobulin expression and the humoral immune response is regulated by the non-canonical poly(A) polymerase TENT5C
title_fullStr Immunoglobulin expression and the humoral immune response is regulated by the non-canonical poly(A) polymerase TENT5C
title_full_unstemmed Immunoglobulin expression and the humoral immune response is regulated by the non-canonical poly(A) polymerase TENT5C
title_short Immunoglobulin expression and the humoral immune response is regulated by the non-canonical poly(A) polymerase TENT5C
title_sort immunoglobulin expression and the humoral immune response is regulated by the non-canonical poly(a) polymerase tent5c
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184606/
https://www.ncbi.nlm.nih.gov/pubmed/32341344
http://dx.doi.org/10.1038/s41467-020-15835-3
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