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Molecular and Cellular Biology, December 1998, p. 7487-7498, Vol. 18, No. 12
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Raf-1 Physically Interacts with Rb and Regulates
Its Function: a Link between Mitogenic Signaling and Cell
Cycle Regulation
Sheng
Wang,
Richik N.
Ghosh,
and
Srikumar P.
Chellappan*
Department of Pathology, College of
Physicians and Surgeons, Columbia University, New York, New York
10032
Received 22 April 1998/Returned for modification 1 June
1998/Accepted 26 August 1998
Cells initiate proliferation in response to growth factor
stimulation, but the biochemical mechanisms linking signals received at
the cell surface receptors to the cell cycle regulatory molecules are
not yet clear. In this study, we show that the signaling molecule Raf-1
can physically interact with Rb and p130 proteins in vitro and in vivo
and that this interaction can be detected in mammalian cells without
overexpressing any component. The binding of Raf-1 to Rb occurs
subsequent to mitogen stimulation, and this interaction can be detected
only in proliferating cells. Raf-1 can inactivate Rb function and can
reverse Rb-mediated repression of E2F1 transcription and cell
proliferation efficiently. The region of Raf-1 involved in Rb binding
spanned residues 1 to 28 at the N terminus, and functional inactivation
of Rb required a direct interaction. Serum stimulation of quiescent
human fibroblast HSF8 cells led to a partial translocation of Raf-1
into the nucleus, where it colocalized with Rb. Further, Raf-1 was able
to phosphorylate Rb in vitro quite efficiently. We believe that the
physical interaction of Raf-1 with Rb is a vital step in the growth
factor-mediated induction of cell proliferation and that Raf-1 acts as
a direct link between cell surface signaling cascades and the cell
cycle machinery.
*
Corresponding author. Mailing address: Department of
Pathology, College of Physicians and Surgeons, Columbia University, 630 W. 168th St., New York, NY 10032. Phone: (212) 305-3736. Fax: (212)
305-5498. E-mail: spc10{at}columbia.edu.

Present address: Cellomics, Inc., Pittsburgh, PA
15238.
Molecular and Cellular Biology, December 1998, p. 7487-7498, Vol. 18, No. 12
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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