© The Rockefeller University Press,
0021-9525/2000//423 $5.00
The Journal of Cell Biology, Volume 149, Number 2,
, 2000 423-430
Suppression of Pyk2 Kinase and Cellular Activities by Fip200
Hiroki Uedaa,
Smita Abbia,
Chuanhai Zhenga, and
Jun-Lin Guana
a Cancer Biology Laboratories, Department of Molecular Medicine, College of Veterinary Medicine, Cornell University, Ithaca, New York 14853
Cancer Biology Laboratories, Department of Molecular Medicine, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853.(607) 253-3708(607) 253-3586
jg19{at}cornell.edu
Proline-rich tyrosine kinase 2 (Pyk2) is a cytoplasmic tyrosine kinase implicated to play a role in several intracellular signaling pathways. We report the identification of a novel Pyk2-interacting protein designated FIP200 (FAK family kinase–interacting protein of 200 kD) by using a yeast two-hybrid screen. In vitro binding assays and coimmunoprecipitation confirmed association of FIP200 with Pyk2, and similar assays also showed FIP200 binding to FAK. However, immunofluorescent staining indicated that FIP200 was predominantly localized in the cytoplasm. FIP200 bound to the kinase domain of Pyk2 and inhibited its kinase activity in in vitro kinase assays. FIP200 also inhibited the kinase activity of the Pyk2 isolated from SYF cells (deficient in Src, Yes, and Fyn expression) and the Pyk2 mutant lacking binding site for Src, suggesting that it regulated Pyk2 kinase directly rather than affecting the associated Src family kinases. Consistent with its inhibitory effect in vitro, FIP200 inhibited activation of Pyk2 and Pyk2-induced apoptosis in intact cells, which correlated with its binding to Pyk2. Finally, activation of Pyk2 by several biological stimuli correlated with the dissociation of endogenous FIP200–Pyk2 complex, which provided further support for inhibition of Pyk2 by FIP200 in intact cells. Together, these results suggest that FIP200 functions as an inhibitor of Pyk2 via binding to its kinase domain.
Key Words: phosphorylation FAK tyrosine kinase inhibitor signal transduction
© 2000 The Rockefeller University Press
Abbreviations used in this paper: CT-FIP, COOH-terminal FIP200; FAK, focal adhesion kinase; FIP200, FAK family kinase–interacting protein of 200 kD; GST, glutathione-S-transferase; HA, hemagglutinin; NT-FIP, NH2-terminal FIP200; Pyk2, proline-rich tyrosine kinase 2.

CiteULike
Complore
Connotea
Del.icio.us
Digg
Facebook
Reddit
Technorati
Twitter What's this?
This article has been cited by other articles:
-
Liang, C.-C., Wang, C., Peng, X., Gan, B., Guan, J.-L.
(2010). Neural-specific Deletion of FIP200 Leads to Cerebellar Degeneration Caused by Increased Neuronal Death and Axon Degeneration. J. Biol. Chem.
285: 3499-3509
[Abstract]
[Full Text]
-
Wei, H., Gan, B., Wu, X., Guan, J.-L.
(2009). Inactivation of FIP200 Leads to Inflammatory Skin Disorder, but Not Tumorigenesis, in Conditional Knock-out Mouse Models. J. Biol. Chem.
284: 6004-6013
[Abstract]
[Full Text]
-
Chen, J., Lu, Y., Meng, S., Han, M.-H., Lin, C., Wang, X.
(2009). {alpha}- and {gamma}-Protocadherins Negatively Regulate PYK2. J. Biol. Chem.
284: 2880-2890
[Abstract]
[Full Text]
-
Hara, T., Takamura, A., Kishi, C., Iemura, S.-i., Natsume, T., Guan, J.-L., Mizushima, N.
(2008). FIP200, a ULK-interacting protein, is required for autophagosome formation in mammalian cells. JCB
181: 497-510
[Abstract]
[Full Text]
-
Xie, J., Allen, K. H., Marguet, A., Berghorn, K. A., Bliss, S. P., Navratil, A. M., Guan, J. L., Roberson, M. S.
(2008). Analysis of the Calcium-Dependent Regulation of Proline-Rich Tyrosine Kinase 2 by Gonadotropin-Releasing Hormone. Mol. Endocrinol.
22: 2322-2335
[Abstract]
[Full Text]
-
Martin, N., Schwamborn, K., Urlaub, H., Gan, B., Guan, J.-L., Dejean, A.
(2008). Spatial Interplay between PIASy and FIP200 in the Regulation of Signal Transduction and Transcriptional Activity. Mol. Cell. Biol.
28: 2771-2781
[Abstract]
[Full Text]
-
Cai, X., Lietha, D., Ceccarelli, D. F., Karginov, A. V., Rajfur, Z., Jacobson, K., Hahn, K. M., Eck, M. J., Schaller, M. D.
(2008). Spatial and Temporal Regulation of Focal Adhesion Kinase Activity in Living Cells. Mol. Cell. Biol.
28: 201-214
[Abstract]
[Full Text]
-
Gudermann, T., Roelle, S.
(2006). Calcium-dependent growth regulation of small cell lung cancer cells by neuropeptides. Endocr Relat Cancer
13: 1069-1084
[Abstract]
[Full Text]
-
Gan, B., Peng, X., Nagy, T., Alcaraz, A., Gu, H., Guan, J.-L.
(2006). Role of FIP200 in cardiac and liver development and its regulation of TNF{alpha} and TSC-mTOR signaling pathways. JCB
175: 121-133
[Abstract]
[Full Text]
-
Gan, B., Melkoumian, Z. K., Wu, X., Guan, K.-L., Guan, J.-L.
(2005). Identification of FIP200 interaction with the TSC1-TSC2 complex and its role in regulation of cell size control. JCB
170: 379-389
[Abstract]
[Full Text]
-
Melkoumian, Z. K., Peng, X., Gan, B., Wu, X., Guan, J.-L.
(2005). Mechanism of Cell Cycle Regulation by FIP200 in Human Breast Cancer Cells. Cancer Res.
65: 6676-6684
[Abstract]
[Full Text]
-
Dunty, J. M., Gabarra-Niecko, V., King, M. L., Ceccarelli, D. F. J., Eck, M. J., Schaller, M. D.
(2004). FERM Domain Interaction Promotes FAK Signaling. Mol. Cell. Biol.
24: 5353-5368
[Abstract]
[Full Text]
-
Heinlein, C. A., Chang, C.
(2004). Androgen Receptor in Prostate Cancer. Endocr. Rev.
25: 276-308
[Abstract]
[Full Text]
-
Cooper, L. A., Shen, T.-L., Guan, J.-L.
(2003). Regulation of Focal Adhesion Kinase by Its Amino-Terminal Domain through an Autoinhibitory Interaction. Mol. Cell. Biol.
23: 8030-8041
[Abstract]
[Full Text]
-
Lipinski, C. A., Tran, N. L., Bay, C., Kloss, J., McDonough, W. S., Beaudry, C., Berens, M. E., Loftus, J. C.
(2003). Differential Role of Proline-Rich Tyrosine Kinase 2 and Focal Adhesion Kinase in Determining Glioblastoma Migration and Proliferation. Mol Cancer Res
1: 323-332
[Abstract]
[Full Text]
-
Abbi, S., Ueda, H., Zheng, C., Cooper, L. A., Zhao, J., Christopher, R., Guan, J.-L.
(2002). Regulation of Focal Adhesion Kinase by a Novel Protein Inhibitor FIP200. Mol. Biol. Cell
13: 3178-3191
[Abstract]
[Full Text]
-
Chellaiah, M. A., Biswas, R. S., Yuen, D., Alvarez, U. M., Hruska, K. A.
(2001). Phosphatidylinositol 3,4,5-Trisphosphate Directs Association of Src Homology 2-containing Signaling Proteins with Gelsolin. J. Biol. Chem.
276: 47434-47444
[Abstract]
[Full Text]