Interaction of Gα12 and Gα13 with the Cytoplasmic Domain of Cadherin Provides a Mechanism for β-Catenin Release
The G12 subfamily of heterotrimeric G proteins, comprised of the α-subunits Gα12 and Gα13, has been implicated as a signaling component in cellular processes ranging from cytoskeletal changes to cell growth and oncogenesis. In an attempt to elucidate specific roles of this subfamily in cell regulati...
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Published in | Proceedings of the National Academy of Sciences - PNAS Vol. 98; no. 2; pp. 519 - 524 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
National Academy of Sciences
16.01.2001
National Acad Sciences The National Academy of Sciences |
Subjects | |
Online Access | Get full text |
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Summary: | The G12 subfamily of heterotrimeric G proteins, comprised of the α-subunits Gα12 and Gα13, has been implicated as a signaling component in cellular processes ranging from cytoskeletal changes to cell growth and oncogenesis. In an attempt to elucidate specific roles of this subfamily in cell regulation, we sought to identify molecular targets of Gα12. Here we show a specific interaction between the G12 subfamily and the cytoplasmic tails of several members of the cadherin family of cell-surface adhesion proteins. Gα12 or Gα13 binding causes dissociation of the transcriptional activator β-catenin from cadherins. Furthermore, in cells lacking the adenomatous polyposis coli protein required for β-catenin degradation, expression of mutationally activated Gα12 or Gα13 causes an increase in β-catenin-mediated transcriptional activation. These findings provide a potential molecular mechanism for the previously reported cellular transforming ability of the G12 subfamily and reveal a link between heterotrimeric G proteins and cellular processes controlling growth and differentiation. |
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Bibliography: | Edited by Melvin I. Simon, California Institute of Technology, Pasadena, CA, and approved November 9, 2000 To whom reprint requests should be addressed. E-mail: casey006@mc.duke.edu. |
ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.98.2.519 |