The SH2-containing protein-tyrosine phosphatase SH-PTP2 is required upstream of MAP kinase for early xenopus development

Terry L. Tang, Robert M. Freeman, Alana M. O'Reilly, Benjamin G. Neel, Sergei Y. Sokol

Research output: Contribution to journalArticlepeer-review

318 Scopus citations

Abstract

SH-PTP2, the vertebrate homolog of Drosophila corkscrew, associates with several activated growth factor receptors, but its biological function is unknown. We assayed the effects of injection of wild-type and mutant SH-PTP2 RNAs on Xenopus embryogenesis. An internal phosphatase domain deletion (ΔP) acts as a dominant negative mutant, causing severe posterior truncations. This phenotype is rescued by SH-PTP2, but not by the closely related SH-PTP1. In ectodermal explants, ΔP blocks fibroblast growth factor (FGF)- and activin-mediated induction of mesoderm and FGF-induced mitogen-activated protein (MAP) kinase activation. Our results indicate that SH-PTP2 is required for early vertebrate development, acting as a positive component in FGF signaling downstream of the FGF receptor and upstream of MAP kinase.

Original languageEnglish
Pages (from-to)473-483
Number of pages11
JournalCell
Volume80
Issue number3
DOIs
StatePublished - Feb 10 1995

Keywords

  • Activins
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Calcium-Calmodulin-Dependent Protein Kinases/genetics
  • Cloning, Molecular
  • Culture Techniques
  • Ectoderm/drug effects
  • Embryonic Induction/drug effects
  • Female
  • Fibroblast Growth Factor 2/pharmacology
  • Inhibins/pharmacology
  • Intracellular Signaling Peptides and Proteins
  • Mesoderm/drug effects
  • Molecular Sequence Data
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11
  • Protein Tyrosine Phosphatase, Non-Receptor Type 6
  • Protein Tyrosine Phosphatases/genetics
  • RNA, Messenger/genetics
  • Sequence Analysis, DNA
  • Sequence Deletion/physiology
  • Xenopus

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