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.
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19 May 1997
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May 19 1997
A Glycine-rich RNA-binding Protein Mediating Cold-inducible Suppression of Mammalian Cell Growth
Hiroyuki Nishiyama,
Hiroyuki Nishiyama
*Department of Clinical Molecular Biology, ‡Department of Urology, Faculty of Medicine, Kyoto University, Kyoto 606, Japan
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Katsuhiko Itoh,
Katsuhiko Itoh
*Department of Clinical Molecular Biology, ‡Department of Urology, Faculty of Medicine, Kyoto University, Kyoto 606, Japan
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Yoshiyuki Kaneko,
Yoshiyuki Kaneko
*Department of Clinical Molecular Biology, ‡Department of Urology, Faculty of Medicine, Kyoto University, Kyoto 606, Japan
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Masamichi Kishishita,
Masamichi Kishishita
*Department of Clinical Molecular Biology, ‡Department of Urology, Faculty of Medicine, Kyoto University, Kyoto 606, Japan
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Osamu Yoshida,
Osamu Yoshida
*Department of Clinical Molecular Biology, ‡Department of Urology, Faculty of Medicine, Kyoto University, Kyoto 606, Japan
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Jun Fujita
Jun Fujita
*Department of Clinical Molecular Biology, ‡Department of Urology, Faculty of Medicine, Kyoto University, Kyoto 606, Japan
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Hiroyuki Nishiyama
*Department of Clinical Molecular Biology, ‡Department of Urology, Faculty of Medicine, Kyoto University, Kyoto 606, Japan
Katsuhiko Itoh
*Department of Clinical Molecular Biology, ‡Department of Urology, Faculty of Medicine, Kyoto University, Kyoto 606, Japan
Yoshiyuki Kaneko
*Department of Clinical Molecular Biology, ‡Department of Urology, Faculty of Medicine, Kyoto University, Kyoto 606, Japan
Masamichi Kishishita
*Department of Clinical Molecular Biology, ‡Department of Urology, Faculty of Medicine, Kyoto University, Kyoto 606, Japan
Osamu Yoshida
*Department of Clinical Molecular Biology, ‡Department of Urology, Faculty of Medicine, Kyoto University, Kyoto 606, Japan
Jun Fujita
*Department of Clinical Molecular Biology, ‡Department of Urology, Faculty of Medicine, Kyoto University, Kyoto 606, Japan
This work was partly supported by Grants-in-Aid from the Ministry of Education, Science, Sports, and Culture of Japan.
Address all correspondence to Jun Fujita, Department of Clinical Molecular Biology, Faculty of Medicine, Kyoto University, Shogoin Kawaharacho, Sakyo-ku, Kyoto 606, Japan. Tel.: 81-75-751-3751. Fax: 81-75-7513750. E-mail: [email protected]
Received:
October 15 1996
Revision Received:
February 27 1997
Online ISSN: 1540-8140
Print ISSN: 0021-9525
1997
J Cell Biol (1997) 137 (4): 899–908.
Article history
Received:
October 15 1996
Revision Received:
February 27 1997
Citation
Hiroyuki Nishiyama, Katsuhiko Itoh, Yoshiyuki Kaneko, Masamichi Kishishita, Osamu Yoshida, Jun Fujita; A Glycine-rich RNA-binding Protein Mediating Cold-inducible Suppression of Mammalian Cell Growth. J Cell Biol 19 May 1997; 137 (4): 899–908. doi: https://doi.org/10.1083/jcb.137.4.899
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