Pin1-dependent prolyl isomerization regulates dephosphorylation of Cdc25C and tau proteins

Mol Cell. 2000 Oct;6(4):873-83. doi: 10.1016/s1097-2765(05)00083-3.

Abstract

The reversible protein phosphorylation on serine or threonine residues that precede proline (pSer/Thr-Pro) is a key signaling mechanism for the control of various cellular processes, including cell division. The pSer/Thr-Pro moiety in peptides exists in the two completely distinct cis and trans conformations whose conversion is catalyzed specifically by the essential prolyl isomerase Pin1. Previous results suggest that Pin1 might regulate the conformation and dephosphorylation of its substrates. However, it is not known whether phosphorylation-dependent prolyl isomerization occurs in a native protein and/or affects dephosphorylation of pSer/Thr-Pro motifs. Here we show that the major Pro-directed phosphatase PP2A is conformation-specific and effectively dephosphorylates only the trans pSer/Thr-Pro isomer. Furthermore, Pin1 catalyzes prolyl isomerization of specific pSer/Thr-Pro motifs both in Cdc25C and tau to facilitate their dephosphorylation by PP2A. Moreover, Pin1 and PP2A show reciprocal genetic interactions, and prolyl isomerase activity of Pin1 is essential for cell division in vivo. Thus, phosphorylation-specific prolyl isomerization catalyzed by Pin1 is a novel mechanism essential for regulating dephosphorylation of certain pSer/Thr-Pro motifs.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Brain / enzymology
  • Cell Cycle Proteins / metabolism*
  • Isomerism
  • Kinetics
  • Mutagenesis
  • Mutagenesis, Site-Directed
  • NIMA-Interacting Peptidylprolyl Isomerase
  • Peptidylprolyl Isomerase / chemistry
  • Peptidylprolyl Isomerase / genetics
  • Peptidylprolyl Isomerase / metabolism*
  • Phosphoprotein Phosphatases / metabolism
  • Phosphorylation
  • Phosphoserine / metabolism
  • Phosphothreonine / metabolism
  • Point Mutation
  • Signal Transduction
  • Substrate Specificity
  • Swine
  • cdc25 Phosphatases / metabolism*
  • tau Proteins / chemistry
  • tau Proteins / metabolism*

Substances

  • Cell Cycle Proteins
  • NIMA-Interacting Peptidylprolyl Isomerase
  • tau Proteins
  • Phosphothreonine
  • Phosphoserine
  • Phosphoprotein Phosphatases
  • cdc25 Phosphatases
  • Peptidylprolyl Isomerase