Affiliation:
1. Division of Signal Transduction, Department of Systems Biology
2. Institut fuer Biochemie, Freie Universitaet Berlin, Berlin, Germany
3. Department of Experimental Oncology, European Institute of Oncology, Milan, Italy
4. Center for Immunology and Department of Molecular Biology and Biochemistry, University of California—Irvine, Irvine, California
5. Cancer Biology Program, Department of Medicine, Beth Israel Deaconness Medical Center, Harvard Medical School, Boston, Massachusetts
Abstract
ABSTRACT
Class Ia phosphoinositide 3-kinases (PI3Ks) are heterodimers of p110 catalytic and p85 regulatory subunits that mediate a variety of cellular responses to growth and differentiation factors. Although embryonic development is not impaired in mice lacking all isoforms of the p85α gene (p85α
−/−
p55α
−/−
p50α
−/−
) or in mice lacking the p85β gene (p85β
−/−
) (D. A. Fruman, F. Mauvais-Jarvis, D. A. Pollard, C. M. Yballe, D. Brazil, R. T. Bronson, C. R. Kahn, and L. C. Cantley, Nat Genet.
26:
379-382, 2000; K. Ueki, C. M. Yballe, S. M. Brachmann, D. Vicent, J. M. Watt, C. R. Kahn, and L. C. Cantley, Proc. Natl. Acad. Sci. USA
99:
419-424, 2002), we show here that loss of both genes results in lethality at embryonic day 12.5 (E12.5). The phenotypes of these embryos, including subepidermal blebs flanking the neural tube at E8 and bleeding into the blebs during the turning process, are similar to defects observed in platelet-derived growth factor receptor α null (PDGFRα
−/−
) mice (P. Soriano, Development
124:
2691-2700, 1997), suggesting that PI3K is an essential mediator of PDGFRα signaling at this developmental stage. p85α
−/−
p55α
+/+
p50α
+/+
p85β
−/−
mice had similar but less severe defects, indicating that p85α and p85β have a critical and redundant function in development. Mouse embryo fibroblasts deficient in all p85α and p85β gene products (p85α
−/−
p55α
−/−
p50α
−/−
p85β
−/−
) are defective in PDGF-induced membrane ruffling. Overexpression of the Rac-specific GDP-GTP exchange factor Vav2 or reintroduction of p85α or p85β rescues the membrane ruffling defect. Surprisingly, reintroduction of p50α also restored PDGF-dependent membrane ruffling. These results indicate that class Ia PI3K is critical for PDGF-dependent actin rearrangement but that the SH3 domain and the Rho/Rac/Cdc42-interacting domain of p85, which lacks p50α, are not required for this response.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
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