Cytokines direct the regulation of Bim and p27^KIP1 mRNA stability by Heat shock cognate protein 70

Matsui Hirotaka

Asou Hiroya

Inaba Toshiya

Molecular Cell

Previous gene-targeting studies indicated that Bim, a BIB-only death activator, and p27^KIP1, a cydin-dependent kinase inhibitor, regulate total cell number in the body. Cytokines contribute to this process primarily by negatively regulating the steady-state levels of Bim and p27 mRNAs. Here we present a novel mechanism for cytokine-mediated post-transcriptional regulation of Bim and p27 mRNA levels via the activity of Heat shock cognate protein 70 (Hsc70), which enhances the stability of specific mRNAs by binding to AU-rich elements (AREs) in their 3' -untranslated regions. The RNA-binding potential of Hsc70 is regulated by co-chaperones, including Bag-4 (also SODD), CHIP, Hip and Hsp40. Cytokines that down-regulate Bim and p27 operate via Ras-activated signaling pathways, which in turn control the expression or function of these co-chaperones. Thus, exposure of cells to cytokines ultimately leads to the destabilization of Bim and p27 mRNAs and the promotion of cell division and survival. This unanticipated role for a chaperone/co-chaperone complex in the control of mRNA stability appears to be critical for hematopoiesis and leukemogenesis.

RNA

SIGNALING

Medical sciences [ 490 ]

eng

Elsevier

Copyright (c) 2007 Elsevier Ltd.

[ISSN] 1097-2765

[DOI] 10.1016/j.molcel.2006.12.007

[NCID] AA1119005X

[DOI] http://dx.doi.org/10.1016/j.molcel.2006.12.007