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Tristetraprolin targets Nos2 expression in the colonic epithelium
Tristetraprolin (TTP), encoded by the Zfp36 gene, is a zinc-finger protein that regulates RNA stability primarily through association with 3′ untranslated regions (3′ UTRs) of target mRNAs. While TTP is expressed abundantly in the intestines, its function in intestinal epithelial cells (IECs) is unk...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783411/ https://www.ncbi.nlm.nih.gov/pubmed/31595002 http://dx.doi.org/10.1038/s41598-019-50957-9 |
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author | Eshelman, Melanie A. Matthews, Stephen M. Schleicher, Emily M. Fleeman, Rebecca M. Kawasawa, Yuka Imamura Stumpo, Deborah J. Blackshear, Perry J. Koltun, Walter A. Ishmael, Faoud T. Yochum, Gregory S. |
author_facet | Eshelman, Melanie A. Matthews, Stephen M. Schleicher, Emily M. Fleeman, Rebecca M. Kawasawa, Yuka Imamura Stumpo, Deborah J. Blackshear, Perry J. Koltun, Walter A. Ishmael, Faoud T. Yochum, Gregory S. |
author_sort | Eshelman, Melanie A. |
collection | PubMed |
description | Tristetraprolin (TTP), encoded by the Zfp36 gene, is a zinc-finger protein that regulates RNA stability primarily through association with 3′ untranslated regions (3′ UTRs) of target mRNAs. While TTP is expressed abundantly in the intestines, its function in intestinal epithelial cells (IECs) is unknown. Here we used a cre-lox system to remove Zfp36 in the mouse epithelium to uncover a role for TTP in IECs and to identify target genes in these cells. While TTP was largely dispensable for establishment and maintenance of the colonic epithelium, we found an expansion of the proliferative zone and an increase in goblet cell numbers in the colon crypts of Zfp36(ΔIEC) mice. Furthermore, through RNA-sequencing of transcripts isolated from the colons of Zfp36(fl/fl) and Zfp36(ΔIEC) mice, we found that expression of inducible nitric oxide synthase (iNos or Nos2) was elevated in TTP-knockout IECs. We demonstrate that TTP interacts with AU-rich elements in the Nos2 3′ UTR and suppresses Nos2 expression. In comparison to control Zfp36(fl/fl) mice, Zfp36(ΔIEC) mice were less susceptible to dextran sodium sulfate (DSS)-induced acute colitis. Together, these results demonstrate that TTP in IECs targets Nos2 expression and aggravates acute colitis. |
format | Online Article Text |
id | pubmed-6783411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67834112019-10-16 Tristetraprolin targets Nos2 expression in the colonic epithelium Eshelman, Melanie A. Matthews, Stephen M. Schleicher, Emily M. Fleeman, Rebecca M. Kawasawa, Yuka Imamura Stumpo, Deborah J. Blackshear, Perry J. Koltun, Walter A. Ishmael, Faoud T. Yochum, Gregory S. Sci Rep Article Tristetraprolin (TTP), encoded by the Zfp36 gene, is a zinc-finger protein that regulates RNA stability primarily through association with 3′ untranslated regions (3′ UTRs) of target mRNAs. While TTP is expressed abundantly in the intestines, its function in intestinal epithelial cells (IECs) is unknown. Here we used a cre-lox system to remove Zfp36 in the mouse epithelium to uncover a role for TTP in IECs and to identify target genes in these cells. While TTP was largely dispensable for establishment and maintenance of the colonic epithelium, we found an expansion of the proliferative zone and an increase in goblet cell numbers in the colon crypts of Zfp36(ΔIEC) mice. Furthermore, through RNA-sequencing of transcripts isolated from the colons of Zfp36(fl/fl) and Zfp36(ΔIEC) mice, we found that expression of inducible nitric oxide synthase (iNos or Nos2) was elevated in TTP-knockout IECs. We demonstrate that TTP interacts with AU-rich elements in the Nos2 3′ UTR and suppresses Nos2 expression. In comparison to control Zfp36(fl/fl) mice, Zfp36(ΔIEC) mice were less susceptible to dextran sodium sulfate (DSS)-induced acute colitis. Together, these results demonstrate that TTP in IECs targets Nos2 expression and aggravates acute colitis. Nature Publishing Group UK 2019-10-08 /pmc/articles/PMC6783411/ /pubmed/31595002 http://dx.doi.org/10.1038/s41598-019-50957-9 Text en © The Author(s) 2019 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 Eshelman, Melanie A. Matthews, Stephen M. Schleicher, Emily M. Fleeman, Rebecca M. Kawasawa, Yuka Imamura Stumpo, Deborah J. Blackshear, Perry J. Koltun, Walter A. Ishmael, Faoud T. Yochum, Gregory S. Tristetraprolin targets Nos2 expression in the colonic epithelium |
title | Tristetraprolin targets Nos2 expression in the colonic epithelium |
title_full | Tristetraprolin targets Nos2 expression in the colonic epithelium |
title_fullStr | Tristetraprolin targets Nos2 expression in the colonic epithelium |
title_full_unstemmed | Tristetraprolin targets Nos2 expression in the colonic epithelium |
title_short | Tristetraprolin targets Nos2 expression in the colonic epithelium |
title_sort | tristetraprolin targets nos2 expression in the colonic epithelium |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783411/ https://www.ncbi.nlm.nih.gov/pubmed/31595002 http://dx.doi.org/10.1038/s41598-019-50957-9 |
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