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RFX transcription factors control a miR-150/PDAP1 axis that restrains the proliferation of human T cells
Within the immune system, microRNAs (miRNAs) exert key regulatory functions. However, what are the mRNA targets regulated by miRNAs and how miRNAs are transcriptionally regulated themselves remain for the most part unknown. We found that in primary human memory T helper lymphocytes, miR-150 was the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865640/ https://www.ncbi.nlm.nih.gov/pubmed/35143476 http://dx.doi.org/10.1371/journal.pbio.3001538 |
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author | Chirichella, Michele Bianchi, Niccolò Džafo, Emina Foli, Elena Gualdrini, Francesco Kenyon, Amy Natoli, Gioacchino Monticelli, Silvia |
author_facet | Chirichella, Michele Bianchi, Niccolò Džafo, Emina Foli, Elena Gualdrini, Francesco Kenyon, Amy Natoli, Gioacchino Monticelli, Silvia |
author_sort | Chirichella, Michele |
collection | PubMed |
description | Within the immune system, microRNAs (miRNAs) exert key regulatory functions. However, what are the mRNA targets regulated by miRNAs and how miRNAs are transcriptionally regulated themselves remain for the most part unknown. We found that in primary human memory T helper lymphocytes, miR-150 was the most abundantly expressed miRNA, and its expression decreased drastically upon activation, suggesting regulatory roles. Constitutive MIR150 gene expression required the RFX family of transcription factors, and its activation-induced down-regulation was linked to their reduced expression. By performing miRNA pull-down and sequencing experiments, we identified PDGFA-associated protein 1 (PDAP1) as one main target of miR-150 in human T lymphocytes. PDAP1 acted as an RNA-binding protein (RBP), and its CRISPR/Cas-9–mediated deletion revealed that it prominently contributed to the regulation of T-cell proliferation. Overall, using an integrated approach involving quantitative analysis, unbiased genomics, and genome editing, we identified RFX factors, miR-150, and the PDAP1 RBP as the components of a regulatory axis that restrains proliferation of primary human T lymphocytes. |
format | Online Article Text |
id | pubmed-8865640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-88656402022-02-24 RFX transcription factors control a miR-150/PDAP1 axis that restrains the proliferation of human T cells Chirichella, Michele Bianchi, Niccolò Džafo, Emina Foli, Elena Gualdrini, Francesco Kenyon, Amy Natoli, Gioacchino Monticelli, Silvia PLoS Biol Research Article Within the immune system, microRNAs (miRNAs) exert key regulatory functions. However, what are the mRNA targets regulated by miRNAs and how miRNAs are transcriptionally regulated themselves remain for the most part unknown. We found that in primary human memory T helper lymphocytes, miR-150 was the most abundantly expressed miRNA, and its expression decreased drastically upon activation, suggesting regulatory roles. Constitutive MIR150 gene expression required the RFX family of transcription factors, and its activation-induced down-regulation was linked to their reduced expression. By performing miRNA pull-down and sequencing experiments, we identified PDGFA-associated protein 1 (PDAP1) as one main target of miR-150 in human T lymphocytes. PDAP1 acted as an RNA-binding protein (RBP), and its CRISPR/Cas-9–mediated deletion revealed that it prominently contributed to the regulation of T-cell proliferation. Overall, using an integrated approach involving quantitative analysis, unbiased genomics, and genome editing, we identified RFX factors, miR-150, and the PDAP1 RBP as the components of a regulatory axis that restrains proliferation of primary human T lymphocytes. Public Library of Science 2022-02-10 /pmc/articles/PMC8865640/ /pubmed/35143476 http://dx.doi.org/10.1371/journal.pbio.3001538 Text en © 2022 Chirichella et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Chirichella, Michele Bianchi, Niccolò Džafo, Emina Foli, Elena Gualdrini, Francesco Kenyon, Amy Natoli, Gioacchino Monticelli, Silvia RFX transcription factors control a miR-150/PDAP1 axis that restrains the proliferation of human T cells |
title | RFX transcription factors control a miR-150/PDAP1 axis that restrains the proliferation of human T cells |
title_full | RFX transcription factors control a miR-150/PDAP1 axis that restrains the proliferation of human T cells |
title_fullStr | RFX transcription factors control a miR-150/PDAP1 axis that restrains the proliferation of human T cells |
title_full_unstemmed | RFX transcription factors control a miR-150/PDAP1 axis that restrains the proliferation of human T cells |
title_short | RFX transcription factors control a miR-150/PDAP1 axis that restrains the proliferation of human T cells |
title_sort | rfx transcription factors control a mir-150/pdap1 axis that restrains the proliferation of human t cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865640/ https://www.ncbi.nlm.nih.gov/pubmed/35143476 http://dx.doi.org/10.1371/journal.pbio.3001538 |
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