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PMID: 9083021 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The Src homology 2 (SH2) domain of SH2-containing inositol phosphatase (SHIP) is essential for tyrosine phosphorylation of SHIP, its association with Shc, and its induction of apoptosis.

The Journal of biological chemistry ·Vol. 272 ·No. 14 ·1997-04-04 ·Pages 8983-8

Liu L, Damen JE, Hughes MR, Babic I, Jirik FR, Krystal G

Abstract

In this study we have investigated the role that the Src homology 2 domain (SH2) of the 145-kDa 5-phosphatase, SH2-containing inositol phosphatase (SHIP), plays in three of the properties that have been associated with this protein following cytokine stimulation: its association with Shc, its tyrosine phosphorylation, and its inhibition of hemopoietic cell growth. In vitro studies using this SH2 domain revealed that it was capable of binding directly to the Tyr(P)317 motif of Shc with a KD of approximately 290 nM, in keeping with other specific SH2/Tyr(P) interactions. In vivo analysis revealed the SH2 and NPXpY motifs of SHIP acted together, with the Tyr(P)317 and phosphotyrosine binding (PTB) domains of Shc, respectively, to ensure a high affinity SHIP.Shc complex. Expression of cDNAs encoding hemagglutinin-tagged wild type and SH2-inactivated forms of SHIP in the murine hemopoietic cell line DA-ER revealed that wild type SHIP becomes both tyrosine-phosphorylated and associated with Shc following interleukin-3 stimulation, as expected, but the SH2-inactivated SHIPs do neither. Moreover, while the growth rates of parental DA-ER cells and cells expressing these various SHIP constructs are identical, the wild type SHIP-expressing cells die, via programmed cell death, far more rapidly than parental cells. Cells expressing SH2-inactivated SHIPs, on the other hand, show either a reduced or no effect on apoptosis. These results suggest that the SH2 domain of SHIP is required not only for the tyrosine phosphorylation of SHIP and Shc association following cytokine stimulation but also for its induction of apoptosis.

MeSH Terms
Animals Apoptosis COS Cells Cell Survival Electrophoresis, Polyacrylamide Gel Mutagenesis Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases Phosphoric Monoester Hydrolases/metabolism Phosphorylation Tyrosine/metabolism src Homology Domains
Chemicals
Tyrosine Phosphoric Monoester Hydrolases INPPL1 protein, human Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Liu L
Terry Fox Laboratory, British Columbia Cancer Agency, and The Biomedical Research Centre, University of British Columbia, Vancouver, British Columbia V5Z 1L3, Canada.
Damen J E
Hughes M R
Babic I
Jirik F R
Krystal G
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1997-04-04
Pages
8983-8
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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