Analysis of molecular determinants of PRL-3

In order to analyse whether a C‐terminal polybasic sequence represents a nuclear localization signal (NLS) we obtained several truncated and mutant forms of protein of regerating liver (PRL)‐3 and evaluated their subcellular localization as compared to the wild‐type form. Our results invalidate the hypothesis that this is an NLS. We also analysed the influence of the C‐ and N‐terminal residues on the phosphatase activity of PRL‐3. Our results provide in vitro evidence that the C‐terminal CAAX motif, besides directing the protein farnesylation, plays an additional regulatory role by inhibiting the catalytic efficiency of PRL‐3. Taking into account the results we obtained, as well as reported data, we propose a hypothetical molecular mechanism for the nucleocytoplasmic localization and transfer of PRL‐3.

[1]  Lydia Tabernero,et al.  Protein tyrosine phosphatases: structure–function relationships , 2008, The FEBS journal.

[2]  Ryan E. Mills,et al.  Classical Nuclear Localization Signals: Definition, Function, and Interaction with Importin α* , 2007, Journal of Biological Chemistry.

[3]  K. Yanagihara,et al.  High PRL-3 expression in human gastric cancer is a marker of metastasis and grades of malignancies: an in situ hybridization study , 2007, Virchows Archiv.

[4]  M. Resh,et al.  Trafficking and signaling by fatty-acylated and prenylated proteins , 2006, Nature chemical biology.

[5]  R. Goody,et al.  Identification and specificity profiling of protein prenyltransferase inhibitors using new fluorescent phosphoisoprenoids. , 2006, Journal of the American Chemical Society.

[6]  D. V. Von Hoff,et al.  PRL phosphatases as potential molecular targets in cancer , 2005, Molecular Cancer Therapeutics.

[7]  A. Bardelli,et al.  PRL-3 Phosphatase Is Implicated in Ovarian Cancer Growth , 2005, Clinical Cancer Research.

[8]  Jae Hoon Kim,et al.  Trimeric structure of PRL-1 phosphatase reveals an active enzyme conformation and regulation mechanisms. , 2005, Journal of molecular biology.

[9]  K. Klinger,et al.  Alterations in Vascular Gene Expression in Invasive Breast Carcinoma , 2004, Cancer Research.

[10]  Qiang Xu,et al.  Phosphatase of regenerating liver-3 promotes motility and metastasis of mouse melanoma cells. , 2004, The American journal of pathology.

[11]  G. Kozlov,et al.  Structural Insights into Molecular Function of the Metastasis-associated Phosphatase PRL-3* , 2004, Journal of Biological Chemistry.

[12]  J. den Hertog,et al.  Dimerization In Vivo and Inhibition of the Nonreceptor Form of Protein Tyrosine Phosphatase Epsilon , 2003, Molecular and Cellular Biology.

[13]  J. Li,et al.  PRL-3 and PRL-1 promote cell migration, invasion, and metastasis. , 2003, Cancer research.

[14]  Jing Wang,et al.  The Tyrosine Phosphatase PRL-1 Localizes to the Endoplasmic Reticulum and the Mitotic Spindle and Is Required for Normal Mitosis* , 2002, The Journal of Biological Chemistry.

[15]  Michael A. Choti,et al.  A Phosphatase Associated with Metastasis of Colorectal Cancer , 2001, Science.

[16]  M. Clarke,et al.  Regulation of p53 localization. , 2001, European journal of biochemistry.

[17]  R. Diamond,et al.  PRL-1 PTPase expression is developmentally regulated with tissue-specific patterns in epithelial tissues. , 2000, American journal of physiology. Gastrointestinal and liver physiology.

[18]  A. Alonso,et al.  Subcellular localization of intracellular protein tyrosine phosphatases in T cells , 2000, European journal of immunology.

[19]  H. Horstmann,et al.  Prenylation-dependent Association of Protein-tyrosine Phosphatases PRL-1, -2, and -3 with the Plasma Membrane and the Early Endosome* , 2000, The Journal of Biological Chemistry.

[20]  B. Kobe Autoinhibition by an internal nuclear localization signal revealed by the crystal structure of mammalian importin α , 1999, Nature Structural Biology.

[21]  Y. Tan,et al.  Mouse PRL-2 and PRL-3, two potentially prenylated protein tyrosine phosphatases homologous to PRL-1. , 1998, Biochemical and biophysical research communications.

[22]  J. Noel,et al.  Structural basis for inhibition of receptor protein-tyrosine phosphatase-α by dimerization , 1996, Nature.

[23]  J. Noel,et al.  Structural basis for inhibition of receptor protein-tyrosine phosphatase-alpha by dimerization. , 1996, Nature.

[24]  R. Taub,et al.  PRL-1, a unique nuclear protein tyrosine phosphatase, affects cell growth , 1994, Molecular and cellular biology.

[25]  C J Marshall,et al.  A CAAX or a CAAL motif and a second signal are sufficient for plasma membrane targeting of ras proteins. , 1991, The EMBO journal.

[26]  R. Laskey,et al.  Two interdependent basic domains in nucleoplasmin nuclear targeting sequence: Identification of a class of bipartite nuclear targeting sequence , 1991, Cell.

[27]  C. Marshall,et al.  A polybasic domain or palmitoylation is required in addition to the CAAX motif to localize p21 ras to the plasma membrane , 1990, Cell.