Cited by 97Protein Tyrosine PhosphatasesCytokine Signaling Pathways and InteractionsProtein Kinase Regulation and GTPase Signaling

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Cloning and characterization of human SHIP, the 145-kD inositol 5- phosphatase that associates with SHC after cytokine stimulation

Ware, MD, Rosten, P, Damen, JE, Liu, L, Humphries, RK, Krystal, G·1996·Blood

DOI 10.1182/blood.v88.8.2833.bloodjournal8882833

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Abstract

We recently cloned and sequenced a cDNA encoding a 145-kD protein from the murine hematopoietic cell line B6SUtA, that becomes tyrosine phosphorylated and associated with Shc after cytokine stimulation. Based on its domains and enzymatic activity, we named this protein SHIP for SH2-containing inositol phosphatase (Damen et al, Proc Natl Acad Sci USA 93:1689, 1996). We describe here the cloning of the human homologue of murine SHIP (mSHIP) from a human megakaryocytic cell line (MO7e) lambda gt11 cDNA library using two nonoverlapping mSHIP cDNA fragments as probes. Northern blot analysis suggests that human SHIP (hSHIP) is expressed as a 5.3-kb mRNA in human bone marrow and a wide variety of other tissues. Sequence analysis of this cDNA predicts a protein of 1188 amino acids exhibiting 87.2% overall sequence identity with mSHIP. Contained within the defined open reading frame is an N-terminal, group l src homology 2 (SH2) domain; three NXXY motifs that, if phosphorylated, could be bound by phosphotyrosine binding (PTB) domains; a C-terminal proline-rich region; and two centrally located inositol polyphosphate 5-phosphatase motifs. Fluorescence in situ hybridization, using the full-length hSHIP cDNA as a probe, mapped hSHIP to the long arm of chromosome 2 at the border between 2q36 and 2q37.

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Authors: Ware, M., Rosten, P., Damen, J., Liu, L., Humphries, R., & Krystal, G.
Affiliations: Terry Fox Laboratory, British Columbia Cancer Research Center, Vancouver, Canada.
ORCID: Liu, L
Humphries, RK
Krystal, G
Venue: Blood
Publisher: American Society of Hematology
Published: 1996-10-15
Volume: 88
Issue: 8
Pages: 2833-2840
ISSN: 0006-4971 (ISSN-L)
1528-0020
DOI: 10.1182/blood.v88.8.2833.bloodjournal8882833
OpenAlex: W2339933169
Cited by: 96
References: 48
Citations by year: 2026: 1 · 2024: 4 · 2023: 5 · 2022: 3 · 2020: 1 · 2019: 2 · 2018: 3 · 2017: 3 · 2016: 1 · 2015: 1 · 2014: 2 · 2013: 2 · 2012: 3
FWCI: 3.03
Type: journal article
Language: en
Open access: closed
Locations: Blood (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Tyrosine Phosphatases
Life Sciences › Immunology and Microbiology › Immunology › Cytokine Signaling Pathways and Interactions
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
Keywords: ships, SH2 domain, phosphotyrosine binding domain, proline-rich region, inositol polyphosphate 5-phosphatase, cytokine induction, tyrosine phosphorylation, gene mapping
MeSH terms: Src Homology 2 Domain-Containing, Transforming Protein 1, Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases, Amino Acid Sequence, Cloning, Molecular, Humans, Leukemia, Megakaryoblastic, Acute, Molecular Sequence Data, Phosphoric Monoester Hydrolases, Phosphorylation, Protein Processing, Post-Translational, Proteins, Tumor Cells, Cultured, Sequence Alignment, Sequence Homology, Amino Acid, In Situ Hybridization, Fluorescence, DNA, Complementary, src Homology Domains, Adaptor Proteins, Vesicular Transport, Adaptor Proteins, Signal Transducing, GRB2 Adaptor Protein, Shc Signaling Adaptor Proteins

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Cloning and characterization of human SHIP, the 145-kD inositol 5- phosphatase that associates with SHC after cytokine stimulation

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