Mice deficient in Rbm38, a target of the p53 family, are susceptible to accelerated aging and spontaneous tumors
Author(s) -
Jin Zhang,
Enshun Xu,
Cong Ren,
Wensheng Yan,
Min Zhang,
Mingyi Chen,
Robert D. Cardiff,
Denise M. Imai,
Erik R. Wisner,
Xinbin Chen
Publication year - 2014
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1415607112
Subject(s) - carcinogenesis , haematopoiesis , biology , translation (biology) , in vivo , rna , messenger rna , repressor , radiosensitivity , cancer research , microbiology and biotechnology , function (biology) , genetics , gene expression , gene , stem cell , medicine , radiation therapy
Significance RNA-binding motif protein 38 (Rbm38) is a target of the p53 family and modulates p53 expression via mRNA translation. However, the biological function of Rbm38 and the role of the p53-Rbm38 loop in tumor suppression have not been studied in vivo. Here, we show that mice deficient inRbm38 exhibit hematopoietic defects and are susceptible to spontaneous tumors and accelerated aging. Furthermore, we show that Rbm38 is critical for p53-mediated radiosensitivity and tumor suppression. Together, our results suggest that Rbm38 is necessary for normal hematopoiesis and for suppressing accelerated aging and tumorigenesis. In addition, the p53-Rbm38 axis might be explored for extending longevity and for tumor suppression.
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