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TENT5 cytoplasmic noncanonical poly(A) polymerases regulate the innate immune response in animals
Innate immunity is the first line of host defense against pathogens. Here, through global transcriptome and proteome analyses, we uncover that newly described cytoplasmic poly(A) polymerase TENT-5 (terminal nucleotidyltransferase 5) enhances the expression of secreted innate immunity effector protei...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668313/ https://www.ncbi.nlm.nih.gov/pubmed/36383655 http://dx.doi.org/10.1126/sciadv.add9468 |
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author | Liudkovska, Vladyslava Krawczyk, Paweł S. Brouze, Aleksandra Gumińska, Natalia Wegierski, Tomasz Cysewski, Dominik Mackiewicz, Zuzanna Ewbank, Jonathan J. Drabikowski, Krzysztof Mroczek, Seweryn Dziembowski, Andrzej |
author_facet | Liudkovska, Vladyslava Krawczyk, Paweł S. Brouze, Aleksandra Gumińska, Natalia Wegierski, Tomasz Cysewski, Dominik Mackiewicz, Zuzanna Ewbank, Jonathan J. Drabikowski, Krzysztof Mroczek, Seweryn Dziembowski, Andrzej |
author_sort | Liudkovska, Vladyslava |
collection | PubMed |
description | Innate immunity is the first line of host defense against pathogens. Here, through global transcriptome and proteome analyses, we uncover that newly described cytoplasmic poly(A) polymerase TENT-5 (terminal nucleotidyltransferase 5) enhances the expression of secreted innate immunity effector proteins in Caenorhabditis elegans. Direct RNA sequencing revealed that multiple mRNAs with signal peptide–encoding sequences have shorter poly(A) tails in tent-5–deficient worms. Those mRNAs are translated at the endoplasmic reticulum where a fraction of TENT-5 is present, implying that they represent its direct substrates. Loss of tent-5 makes worms more susceptible to bacterial infection. Notably, the role of TENT-5 in innate immunity is evolutionarily conserved. Its orthologs, TENT5A and TENT5C, are expressed in macrophages and induced during their activation. Analysis of macrophages devoid of TENT5A/C revealed their role in the regulation of secreted proteins involved in defense response. In summary, our study reveals cytoplasmic polyadenylation to be a previously unknown component of the posttranscriptional regulation of innate immunity in animals. |
format | Online Article Text |
id | pubmed-9668313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-96683132022-11-29 TENT5 cytoplasmic noncanonical poly(A) polymerases regulate the innate immune response in animals Liudkovska, Vladyslava Krawczyk, Paweł S. Brouze, Aleksandra Gumińska, Natalia Wegierski, Tomasz Cysewski, Dominik Mackiewicz, Zuzanna Ewbank, Jonathan J. Drabikowski, Krzysztof Mroczek, Seweryn Dziembowski, Andrzej Sci Adv Biomedicine and Life Sciences Innate immunity is the first line of host defense against pathogens. Here, through global transcriptome and proteome analyses, we uncover that newly described cytoplasmic poly(A) polymerase TENT-5 (terminal nucleotidyltransferase 5) enhances the expression of secreted innate immunity effector proteins in Caenorhabditis elegans. Direct RNA sequencing revealed that multiple mRNAs with signal peptide–encoding sequences have shorter poly(A) tails in tent-5–deficient worms. Those mRNAs are translated at the endoplasmic reticulum where a fraction of TENT-5 is present, implying that they represent its direct substrates. Loss of tent-5 makes worms more susceptible to bacterial infection. Notably, the role of TENT-5 in innate immunity is evolutionarily conserved. Its orthologs, TENT5A and TENT5C, are expressed in macrophages and induced during their activation. Analysis of macrophages devoid of TENT5A/C revealed their role in the regulation of secreted proteins involved in defense response. In summary, our study reveals cytoplasmic polyadenylation to be a previously unknown component of the posttranscriptional regulation of innate immunity in animals. American Association for the Advancement of Science 2022-11-16 /pmc/articles/PMC9668313/ /pubmed/36383655 http://dx.doi.org/10.1126/sciadv.add9468 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Liudkovska, Vladyslava Krawczyk, Paweł S. Brouze, Aleksandra Gumińska, Natalia Wegierski, Tomasz Cysewski, Dominik Mackiewicz, Zuzanna Ewbank, Jonathan J. Drabikowski, Krzysztof Mroczek, Seweryn Dziembowski, Andrzej TENT5 cytoplasmic noncanonical poly(A) polymerases regulate the innate immune response in animals |
title | TENT5 cytoplasmic noncanonical poly(A) polymerases regulate the innate immune response in animals |
title_full | TENT5 cytoplasmic noncanonical poly(A) polymerases regulate the innate immune response in animals |
title_fullStr | TENT5 cytoplasmic noncanonical poly(A) polymerases regulate the innate immune response in animals |
title_full_unstemmed | TENT5 cytoplasmic noncanonical poly(A) polymerases regulate the innate immune response in animals |
title_short | TENT5 cytoplasmic noncanonical poly(A) polymerases regulate the innate immune response in animals |
title_sort | tent5 cytoplasmic noncanonical poly(a) polymerases regulate the innate immune response in animals |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668313/ https://www.ncbi.nlm.nih.gov/pubmed/36383655 http://dx.doi.org/10.1126/sciadv.add9468 |
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