Cargando…
A Glycine-rich RNA-binding Protein Mediating Cold-inducible Suppression of Mammalian Cell Growth
In response to low ambient temperature, mammalian cells as well as microorganisms change various physiological functions, but the molecular mechanisms underlying these adaptations are just beginning to be understood. We report here the isolation of a mouse cold-inducible RNA-binding protein (cirp) c...
Autores principales: | , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1997
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139845/ https://www.ncbi.nlm.nih.gov/pubmed/9151692 |
_version_ | 1782143891292553216 |
---|---|
author | Nishiyama, Hiroyuki Itoh, Katsuhiko Kaneko, Yoshiyuki Kishishita, Masamichi Yoshida, Osamu Fujita, Jun |
author_facet | Nishiyama, Hiroyuki Itoh, Katsuhiko Kaneko, Yoshiyuki Kishishita, Masamichi Yoshida, Osamu Fujita, Jun |
author_sort | Nishiyama, Hiroyuki |
collection | PubMed |
description | In response to low ambient temperature, mammalian cells as well as microorganisms change various physiological functions, but the molecular mechanisms underlying these adaptations are just beginning to be understood. We report here the isolation of a mouse cold-inducible RNA-binding protein (cirp) cDNA and investigation of its role in cold-stress response of mammalian cells. The cirp cDNA encoded an 18-kD protein consisting of an amino-terminal RNAbinding domain and a carboxyl-terminal glycine-rich domain and exhibited structural similarity to a class of stress-induced RNA-binding proteins found in plants. Immunofluorescence microscopy showed that CIRP was localized in the nucleoplasm of BALB/3T3 mouse fibroblasts. When the culture temperature was lowered from 37 to 32°C, expression of CIRP was induced and growth of BALB/3T3 cells was impaired as compared with that at 37°C. By suppressing the induction of CIRP with antisense oligodeoxynucleotides, this impairment was alleviated, while overexpression of CIRP resulted in impaired growth at 37°C with prolongation of G1 phase of the cell cycle. These results indicate that CIRP plays an essential role in cold-induced growth suppression of mouse fibroblasts. Identification of CIRP may provide a clue to the regulatory mechanisms of cold responses in mammalian cells. |
format | Text |
id | pubmed-2139845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21398452008-05-01 A Glycine-rich RNA-binding Protein Mediating Cold-inducible Suppression of Mammalian Cell Growth Nishiyama, Hiroyuki Itoh, Katsuhiko Kaneko, Yoshiyuki Kishishita, Masamichi Yoshida, Osamu Fujita, Jun J Cell Biol Article In response to low ambient temperature, mammalian cells as well as microorganisms change various physiological functions, but the molecular mechanisms underlying these adaptations are just beginning to be understood. We report here the isolation of a mouse cold-inducible RNA-binding protein (cirp) cDNA and investigation of its role in cold-stress response of mammalian cells. The cirp cDNA encoded an 18-kD protein consisting of an amino-terminal RNAbinding domain and a carboxyl-terminal glycine-rich domain and exhibited structural similarity to a class of stress-induced RNA-binding proteins found in plants. Immunofluorescence microscopy showed that CIRP was localized in the nucleoplasm of BALB/3T3 mouse fibroblasts. When the culture temperature was lowered from 37 to 32°C, expression of CIRP was induced and growth of BALB/3T3 cells was impaired as compared with that at 37°C. By suppressing the induction of CIRP with antisense oligodeoxynucleotides, this impairment was alleviated, while overexpression of CIRP resulted in impaired growth at 37°C with prolongation of G1 phase of the cell cycle. These results indicate that CIRP plays an essential role in cold-induced growth suppression of mouse fibroblasts. Identification of CIRP may provide a clue to the regulatory mechanisms of cold responses in mammalian cells. The Rockefeller University Press 1997-05-19 /pmc/articles/PMC2139845/ /pubmed/9151692 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Nishiyama, Hiroyuki Itoh, Katsuhiko Kaneko, Yoshiyuki Kishishita, Masamichi Yoshida, Osamu Fujita, Jun A Glycine-rich RNA-binding Protein Mediating Cold-inducible Suppression of Mammalian Cell Growth |
title | A Glycine-rich RNA-binding Protein Mediating Cold-inducible Suppression of Mammalian Cell Growth |
title_full | A Glycine-rich RNA-binding Protein Mediating Cold-inducible Suppression of Mammalian Cell Growth |
title_fullStr | A Glycine-rich RNA-binding Protein Mediating Cold-inducible Suppression of Mammalian Cell Growth |
title_full_unstemmed | A Glycine-rich RNA-binding Protein Mediating Cold-inducible Suppression of Mammalian Cell Growth |
title_short | A Glycine-rich RNA-binding Protein Mediating Cold-inducible Suppression of Mammalian Cell Growth |
title_sort | glycine-rich rna-binding protein mediating cold-inducible suppression of mammalian cell growth |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139845/ https://www.ncbi.nlm.nih.gov/pubmed/9151692 |
work_keys_str_mv | AT nishiyamahiroyuki aglycinerichrnabindingproteinmediatingcoldinduciblesuppressionofmammaliancellgrowth AT itohkatsuhiko aglycinerichrnabindingproteinmediatingcoldinduciblesuppressionofmammaliancellgrowth AT kanekoyoshiyuki aglycinerichrnabindingproteinmediatingcoldinduciblesuppressionofmammaliancellgrowth AT kishishitamasamichi aglycinerichrnabindingproteinmediatingcoldinduciblesuppressionofmammaliancellgrowth AT yoshidaosamu aglycinerichrnabindingproteinmediatingcoldinduciblesuppressionofmammaliancellgrowth AT fujitajun aglycinerichrnabindingproteinmediatingcoldinduciblesuppressionofmammaliancellgrowth AT nishiyamahiroyuki glycinerichrnabindingproteinmediatingcoldinduciblesuppressionofmammaliancellgrowth AT itohkatsuhiko glycinerichrnabindingproteinmediatingcoldinduciblesuppressionofmammaliancellgrowth AT kanekoyoshiyuki glycinerichrnabindingproteinmediatingcoldinduciblesuppressionofmammaliancellgrowth AT kishishitamasamichi glycinerichrnabindingproteinmediatingcoldinduciblesuppressionofmammaliancellgrowth AT yoshidaosamu glycinerichrnabindingproteinmediatingcoldinduciblesuppressionofmammaliancellgrowth AT fujitajun glycinerichrnabindingproteinmediatingcoldinduciblesuppressionofmammaliancellgrowth |