Premium
A functional network of the tumor suppressors APC, hDlg, and PTEN, that relies on recognition of specific PDZ‐domains
Author(s) -
Sotelo Natalia S.,
Valiente Miguel,
Gil Anabel,
Pulido Rafael
Publication year - 2012
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.24141
Subject(s) - pdz domain , pten , scaffold protein , suppressor , microbiology and biotechnology , carcinogenesis , biology , cancer research , protein–protein interaction , pi3k/akt/mtor pathway , signal transduction , cancer , genetics
APC and PTEN are tumor suppressor proteins that bind through their C‐termini to the PDZ domain containing‐hDlg scaffolding protein. We have found that co‐expression of PTEN and hDlg enhanced the negative regulation of the PI3K/Akt pathway by PTEN, indicating the physiologic importance of these interactions. APC and PTEN share other PDZ domain containing–interacting partners, including the MAGI scaffolding proteins and the MAST family of protein kinases. Mutational analysis revealed that the C‐terminal PDZ‐binding motifs from APC and PTEN were differentially recognized by distinct PDZ domains. APC bound to the three PDZ domains from hDlg, whereas PTEN mainly bound to PDZ‐2/hDlg. This indicates the existence of overlapping, but distinct PDZ‐domain recognition patterns by APC and PTEN. Furthermore, a ternary complex formed by APC, PTEN, and hDlg was detected, suggesting that hDlg may serve as a platform to bring in proximity APC and PTEN tumor suppressor activities. In line with this, tumor‐related mutations targeting the PDZ‐2/hDlg domain diminished its interaction with APC and PTEN. Our results expand the PDZ‐domain counterparts for the tumor suppressor APC, show that APC and PTEN share PDZ‐domain partners but have individual molecular determinants for specific recognition of PDZ domains, and suggest the participation of the tumor suppressors APC, PTEN, and hDlg in PDZ‐domain interaction networks which may be relevant in oncogenesis. J. Cell. Biochem. 113: 2661–2670, 2012. © 2012 Wiley Periodicals, Inc.