Literature DB >> 1651716

Identification of skeletal muscle protein-tyrosine phosphatases by amplification of conserved cDNA sequences.

W R Zhang1, B J Goldstein.   

Abstract

Specific protein-tyrosine phosphatase (PTPase) enzymes that regulate signal transduction by the insulin receptor in target tissues have not been identified. We evaluated the expression of PTPase homologs in skeletal muscle since this tissue is the major site of insulin-mediated glucose disposal in vivo. A rat skeletal muscle cDNA pool was prepared with a set of degenerate oligonucleotide primers and PTPase cDNA sequences were amplified using pairs of "guess-mers" that were deduced from highly conserved residues within the known catalytic domains of these enzymes. Sequences encoding three "receptor-like" transmembrane PTPases were identified and two of these (known as LAR and LRP) were confirmed to be expressed in muscle by subsequent cDNA library screening and Northern blot analysis. The expression of the LAR and LRP PTPases in skeletal muscle suggests that these enzymes might have a role in the regulation of insulin action in muscle and other insulin-sensitive tissues.

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Year:  1991        PMID: 1651716     DOI: 10.1016/0006-291x(91)91034-a

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  6 in total

1.  Secreted VAPB/ALS8 major sperm protein domains modulate mitochondrial localization and morphology via growth cone guidance receptors.

Authors:  Sung Min Han; Hiroshi Tsuda; Youfeng Yang; Jack Vibbert; Pauline Cottee; Se-Jin Lee; Jessica Winek; Claire Haueter; Hugo J Bellen; Michael A Miller
Journal:  Dev Cell       Date:  2012-01-19       Impact factor: 12.270

2.  Insulin receptor and epidermal growth factor receptor dephosphorylation by three major rat liver protein-tyrosine phosphatases expressed in a recombinant bacterial system.

Authors:  N Hashimoto; W R Zhang; B J Goldstein
Journal:  Biochem J       Date:  1992-06-01       Impact factor: 3.857

Review 3.  Receptor-like protein tyrosine phosphatases: alike and yet so different.

Authors:  R Schaapveld; B Wieringa; W Hendriks
Journal:  Mol Biol Rep       Date:  1997-11       Impact factor: 2.316

Review 4.  Regulation of the insulin signalling pathway by cellular protein-tyrosine phosphatases.

Authors:  B J Goldstein; F Ahmad; W Ding; P M Li; W R Zhang
Journal:  Mol Cell Biochem       Date:  1998-05       Impact factor: 3.396

5.  Identification and typing of members of the protein-tyrosine phosphatase gene family expressed in mouse brain.

Authors:  J Schepens; P Zeeuwen; B Wieringa; W Hendriks
Journal:  Mol Biol Rep       Date:  1992-09       Impact factor: 2.316

6.  LAR tyrosine phosphatase receptor: alternative splicing is preferential to the nervous system, coordinated with cell growth and generates novel isoforms containing extensive CAG repeats.

Authors:  J S Zhang; F M Longo
Journal:  J Cell Biol       Date:  1995-02       Impact factor: 10.539

  6 in total

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