Literature DB >> 12837292

PTPRQ is a novel phosphatidylinositol phosphatase that can be expressed as a cytoplasmic protein or as a subcellularly localized receptor-like protein.

R A Seifert1, S A Coats, A Oganesian, M B Wright, M Dishmon, C J Booth, R J Johnson, C E Alpers, D F Bowen-Pope.   

Abstract

PTPRQ (rPTP-GMC1) is a member of the type III receptor-like protein tyrosine phosphatase family. PTPRQ has very low activity against phosphotyrosine but is active against phosphatidylinositol phosphates that are involved in regulation of survival, proliferation, and subcellular architecture. Here, we report that PTPRQ can be expressed as a cytosolic or a receptor-like protein and that the form, subcellular localization, and cell types in which it is expressed are regulated by alternative promoter use and by alternative splicing. The first promoter drives expression of transcripts encoding a transmembrane protein in human podocytes and lung. PTPRQ protein is localized to the basal membrane of human podocytes, beginning when podocyte progenitors can first be identified in the embryonic kidney. A second promoter drives expression of a transcript that can encode a cytoplasmic protein containing the catalytic site. This is the major PTPRQ transcript in rat mesangial cells and human testis and is upregulated in mesangial cells in a rat model of mesangial proliferative glomerulonephritis. Differential regulation of expression of the transmembrane vs cytosolic forms, in different cell types during development or response to injury, may be a mechanism through which PTPRQ, with its activities against membrane phospholipids and against phosphotyrosine, can target specific substrates under different conditions.

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Year:  2003        PMID: 12837292     DOI: 10.1016/s0014-4827(03)00121-6

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  10 in total

1.  Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunction.

Authors:  Margit Schraders; Jaap Oostrik; Patrick L M Huygen; Tim M Strom; Erwin van Wijk; Henricus P M Kunst; Lies H Hoefsloot; Cor W R J Cremers; Ronald J C Admiraal; Hannie Kremer
Journal:  Am J Hum Genet       Date:  2010-03-25       Impact factor: 11.025

Review 2.  Protein tyrosine phosphatases: structure, function, and implication in human disease.

Authors:  Lutz Tautz; David A Critton; Stefan Grotegut
Journal:  Methods Mol Biol       Date:  2013

Review 3.  Autosomal recessive nonsyndromic deafness genes: a review.

Authors:  Duygu Duman; Mustafa Tekin
Journal:  Front Biosci (Landmark Ed)       Date:  2012-06-01

4.  Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereocilia.

Authors:  Kenneth R Johnson; Chantal M Longo-Guess; Leona H Gagnon
Journal:  PLoS One       Date:  2012-04-27       Impact factor: 3.240

Review 5.  Voltage sensitive phosphatases: emerging kinship to protein tyrosine phosphatases from structure-function research.

Authors:  Kirstin Hobiger; Thomas Friedrich
Journal:  Front Pharmacol       Date:  2015-01-10       Impact factor: 5.810

6.  PTPRQ as a potential biomarker for idiopathic normal pressure hydrocephalus.

Authors:  Yuki Nagata; Masahiko Bundo; Saiko Sugiura; Masahiro Kamita; Masaya Ono; Kotaro Hattori; Sumiko Yoshida; Yu-Ichi Goto; Katsuya Urakami; Shumpei Niida
Journal:  Mol Med Rep       Date:  2017-07-15       Impact factor: 2.952

7.  Phosphotyrosine phosphatase R3 receptors: Origin, evolution and structural diversification.

Authors:  Javier U Chicote; Rob DeSalle; Antonio García-España
Journal:  PLoS One       Date:  2017-03-03       Impact factor: 3.240

8.  Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family.

Authors:  Xue Gao; Yu Su; Yu-Lan Chen; Ming-Yu Han; Yong-Yi Yuan; Jin-Cao Xu; Feng Xin; Mei-Guang Zhang; Sha-Sha Huang; Guo-Jian Wang; Dong-Yang Kang; Li-Ping Guan; Jian-Guo Zhang; Pu Dai
Journal:  PLoS One       Date:  2015-04-28       Impact factor: 3.240

9.  Identification of novel PTPRQ phosphatase inhibitors based on the virtual screening with docking simulations.

Authors:  Hwangseo Park; Keum Ran Yu; Bonsu Ku; Bo Yeon Kim; Seung Jun Kim
Journal:  Theor Biol Med Model       Date:  2013-08-28       Impact factor: 2.432

10.  First confirmatory study on PTPRQ as an autosomal dominant non-syndromic hearing loss gene.

Authors:  Dominika Oziębło; Anna Sarosiak; Marcin L Leja; Birgit S Budde; Grażyna Tacikowska; Nataliya Di Donato; Hanno J Bolz; Peter Nürnberg; Henryk Skarżyński; Monika Ołdak
Journal:  J Transl Med       Date:  2019-10-26       Impact factor: 5.531

  10 in total

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