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{{Infobox_gene}}
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'''Receptor-type tyrosine-protein phosphatase PCP-2''' (also known as PTP-pi, PTP lambda, hPTP-J, PTPRO and PTP psi), is an [[enzyme]] that in humans is encoded by the ''PTPRU'' [[gene]].<ref name="pmid8700514">{{cite journal |vauthors=Wang H, Lian Z, Lerch MM, Chen Z, Xie W, Ullrich A | title = Characterization of PCP-2, a novel receptor protein tyrosine phosphatase of the MAM domain family | journal = Oncogene | volume = 12 | issue = 12 | pages = 2555–62 |date=Sep 1996 | pmid = 8700514 | pmc =  | doi =  }}</ref><ref name="pmid9434160">{{cite journal |vauthors=Avraham S, London R, Tulloch GA, Ellis M, Fu Y, Jiang S, White RA, Painter C, Steinberger AA, Avraham H | title = Characterization and chromosomal localization of PTPRO, a novel receptor protein tyrosine phosphatase, expressed in hematopoietic stem cells | journal = Gene | volume = 204 | issue = 1–2 | pages = 5–16 |date=Feb 1998 | pmid = 9434160 | pmc = | doi = 10.1016/S0378-1119(97)00420-4}}</ref><ref name="entrez">{{cite web | title = Entrez Gene: PTPRU protein tyrosine phosphatase, receptor type, U| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10076| accessdate = }}</ref>
| update_page = yes
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| update_protein_box = yes
| update_summary = yes
| update_citations = yes
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<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
== Function ==
{{GNF_Protein_box
| image =
| image_source =
| PDB =
| Name = Protein tyrosine phosphatase, receptor type, U
| HGNCid = 9683
| Symbol = PTPRU
| AltSymbols =; PTPRO; GLEPP1; PTPU2; PTP; FLJ37530; FMI; PCP-2; PTP-J; PTP-PI; PTPPSI; R-PTP-PSI; hPTP-J
| OMIM = 602454
| ECnumber = 
| Homologene = 4168
| MGIid = 1321151
| GeneAtlas_image1 = PBB_GE_PTPRU_211320_s_at_tn.png
| Function = {{GNF_GO|id=GO:0004725 |text = protein tyrosine phosphatase activity}} {{GNF_GO|id=GO:0004872 |text = receptor activity}} {{GNF_GO|id=GO:0005001 |text = transmembrane receptor protein tyrosine phosphatase activity}} {{GNF_GO|id=GO:0016787 |text = hydrolase activity}}
| Component = {{GNF_GO|id=GO:0005575 |text = cellular_component}} {{GNF_GO|id=GO:0005887 |text = integral to plasma membrane}} {{GNF_GO|id=GO:0016020 |text = membrane}} {{GNF_GO|id=GO:0016021 |text = integral to membrane}}
| Process = {{GNF_GO|id=GO:0006470 |text = protein amino acid dephosphorylation}} {{GNF_GO|id=GO:0007155 |text = cell adhesion}} {{GNF_GO|id=GO:0007185 |text = transmembrane receptor protein tyrosine phosphatase signaling pathway}} {{GNF_GO|id=GO:0008150 |text = biological_process}}
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 10076
    | Hs_Ensembl = ENSG00000060656
    | Hs_RefseqProtein = NP_005695
    | Hs_RefseqmRNA = NM_005704
    | Hs_GenLoc_db = 
    | Hs_GenLoc_chr = 1
    | Hs_GenLoc_start = 29435615
    | Hs_GenLoc_end = 29525899
    | Hs_Uniprot = Q92729
    | Mm_EntrezGene = 19273
    | Mm_Ensembl = ENSMUSG00000028909
    | Mm_RefseqmRNA = NM_011214
    | Mm_RefseqProtein = NP_035344
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 4
    | Mm_GenLoc_start = 131040533
    | Mm_GenLoc_end = 131110364
    | Mm_Uniprot = 
  }}
}}
'''Protein tyrosine phosphatase, receptor type, U''', also known as '''PTPRU''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: PTPRU protein tyrosine phosphatase, receptor type, U| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10076| accessdate = }}</ref>


<!-- The PBB_Summary template is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and two tandem intracellular catalytic tyrosine phosphatase domains, and thus represents a receptor-type PTP (RPTP). The extracellular region contains a meprin-A5 antigen-PTPmu (MAM) domain, one Ig-like domain and four fibronectin type III-like repeats, and thus is a member of the type R2B RPTP family. It was cloned by many groups and given different names, including PCP-2,<ref name="pmid8700514"/> PTP pi,<ref name="pmid8870675">{{cite journal|vauthors=Crossland S, Smith PD, Crompton MR | title=Molecular cloning and characterization of PTP pi, a novel receptor-like protein-tyrosine phosphatase | journal=Biochem J | year= 1996 | volume= 319 | issue=  1| pages= 249–54 | pmid=8870675 | doi= | pmc=1217761 }}</ref> PTP lambda,<ref name="pmid9054423">{{cite journal|vauthors=Cheng J, Wu K, Armanini M, O'Rourke N, Dowbenko D, Lasky LA | title=A novel protein-tyrosine phosphatase related to the homotypically adhering kappa and mu receptors | journal=J Biol Chem | year= 1997 | volume= 272 | issue= 11 | pages= 7264–77 | pmid=9054423 | doi= 10.1074/jbc.272.11.7264 }}</ref> hPTP-J,<ref name="pmid9070223">{{cite journal|vauthors=Wang B, Kishihara K, Zhang D, Hara H, Nomoto K | title=Molecular cloning and characterization of a novel human receptor protein tyrosine phosphatase gene, hPTP-J: down-regulation of gene expression by PMA and calcium ionophore in Jurkat T lymphoma cells | journal=Biochem Biophys Res Commun | year= 1997 | volume= 231 | issue= 1 | pages= 77–81 | pmid=9070223 | doi=10.1006/bbrc.1997.6004 }}</ref> PTPRO,<ref name="pmid9434160"/> and PTP psi.<ref name="pmid12799079">{{cite journal|vauthors=Aerne B, Stoker A, Ish-Horowicz D | title=Chick receptor tyrosine phosphatase Psi is dynamically expressed during somitogenesis | journal=Gene Expr Patterns | year= 2003 | volume= 3 | issue= 3 | pages= 325–9 | pmid=12799079 | doi= 10.1016/S1567-133X(03)00038-3 }}</ref> Other type R2B RPTPs include [[PTPRM]], [[PTPRK]], and [[PTPRT]]. Analysis of the genomic structure of PCP-2 suggests that it is the most distantly related of the type R2B RPTPS.<ref name="pmid15040814">{{cite journal|vauthors=Besco J, Popesco MC, Davuluri RV, Frostholm A, Rotter A | title=Genomic structure and alternative splicing of murine R2B receptor protein tyrosine phosphatases (PTPkappa, mu, rho and PCP-2) | journal=BMC Genomics | year= 2004 | volume= 5 | pages= 14 | pmid=15040814 | doi=10.1186/1471-2164-5-14 | pmc=373446 | issue=1}}</ref>
{{PBB_Summary
 
| section_title =
RPTPs are able to remove phosphate moieties from tyrosine residues.  Although the R2B family of RPTPs are characterized as having two tyrosine phosphatase domains in their intracellular domain, usually only one is catalytically active.<ref name="pmid12506125">{{cite journal|vauthors=Johnson KG, Van Vactor D | title=Receptor protein tyrosine phosphatases in nervous system development | journal=Physiol Rev | year= 2003 | volume= 83 | issue= 1 | pages= 1–24 | pmid=12506125 | doi=10.1152/physrev.00016.2002 }}</ref><ref name="pmid15464569">{{cite journal|vauthors=Ensslen-Craig SE, Brady-Kalnay SM | title=Receptor protein tyrosine phosphatases regulate neural development and axon guidance | journal=Dev Biol | year= 2004 | volume= 275 | issue= 1 | pages= 12–22 | pmid=15464569 | doi=10.1016/j.ydbio.2004.08.009 }}</ref>  A point mutation study suggests that only the first phosphatase domain of PCP-2 is catalytically active and able to dephosphorylate β-catenin.<ref name="pmid12501215">{{cite journal |vauthors=Yan HX, He YQ, Dong H, Zhang P, Zeng JZ, Cao HF, etal | title=Physical and functional interaction between receptor-like protein tyrosine phosphatase PCP-2 and beta-catenin | journal=Biochemistry | year= 2002 | volume= 41 | issue= 52 | pages= 15854–60 | pmid=12501215 | doi= 10.1021/bi026095u }}</ref> A recombinant protein with both PCP-2 phosphatase domains was also able to dephosphorylate EGFR.<ref name="pmid8870675" /> However, when each of the two intracellular catalytic tyrosine phosphatase domains are expressed individually as recombinant proteins and assayed in vitro using the artificial substrate ρ-nitrophenol phosphate (pNPP), both the first and second intracellular tyrosine phosphatase domain were able to dephosphorylate pNPP.<ref name="pmid8870675" />
| summary_text = The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and two tandem intracellular catalytic domains, and thus represents a receptor-type PTP. The extracellular region contains a meprin-A5 antigen-PTP (MAM) domain, Ig-like and fibronectin type III-like repeats. This PTP was thought to play roles in cell-cell recognition and adhesion. Studies of the similar gene in mice suggested the role of this PTP in early neural development. The expression of this gene was reported to be regulated by phorbol myristate acetate (PMA) or calcium ionophore in Jurkat T lymphoma cells. Three alternatively spliced transcript variants, which encode distinct proteins, have been reported.<ref name="entrez">{{cite web | title = Entrez Gene: PTPRU protein tyrosine phosphatase, receptor type, U| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10076| accessdate = }}</ref>
 
}}
== Regulation ==
 
PCP-2 mRNA is regulated by phorbol myristate acetate (PMA) or calcium ionophore, okadaic acid, the Ras inhibitor manumycin, and orthovanadate in Jurkat T lymphoma cells.<ref name="pmid9070223" /><ref name="pmid10395944">{{cite journal|vauthors=Wang B, Kishihara K, Zhang D, Sakamoto T, Nomoto K | title=Transcriptional regulation of a receptor protein tyrosine phosphatase gene hPTP-J by PKC-mediated signaling pathways in Jurkat and Molt-4 T lymphoma cells | journal=Biochim Biophys Acta | year= 1999 | volume= 1450 | issue= 3 | pages= 331–40 | pmid=10395944 | doi= 10.1016/S0167-4889(99)00064-6 }}</ref>
 
== Alternative splicing ==
 
Four alternatively spliced transcript variants, which encode distinct proteins, have been reported.<ref name="entrez"/>
 
Examination of mouse full-length cDNA sequences for alternatively spliced phosphatase genes identified two novel forms of PTPRU predicted to result in two PCP-2 splice variants: a tethered variant of PCP-2, expressing an intact extracellular and transmembrane domain, and a PCP-2 variant that lacked a signal peptide, but encoded intact transmembrane and cytoplasmic domains.<ref name="pmid16507138">{{cite journal |vauthors=Forrest AR, Taylor DF, Crowe ML, Chalk AM, Waddell NJ, Kolle G, etal | title=Genome-wide review of transcriptional complexity in mouse protein kinases and phosphatases | journal=Genome Biol | year= 2006 | volume= 7 | issue= 1 | pages= R5 | pmid=16507138 | doi=10.1186/gb-2006-7-1-r5 | pmc = 1431701 }}</ref>
 
== Homophilic binding ==
 
The MAM, Ig and first fibronectin III domain of PCP-2 was shown to mediate bead aggregation in vitro.<ref name="pmid9054423" /> PCP-2 accomplishes this by binding to another PCP-2 molecule on a fluorescent bead, known as homophilic binding.  PCP-2 was unable to mediate aggregation between non-adherent cells when expressed as a full-length protein, however, suggesting that PCP-2 does not mediate homophilic adhesion in cells.<ref name="pmid20521994">{{cite journal|vauthors=Becka S, Zhang P, Craig SE, Lodowski DT, Wang Z, Brady-Kalnay SM | title=Characterization of the adhesive properties of the type IIb subfamily receptor protein tyrosine phosphatases | journal=Cell Commun Adhes | year= 2010 | volume= 17 | issue= 2 | pages= 34–47 | pmid=20521994 | doi=10.3109/15419061.2010.487957 | pmc=3337334 }}</ref> The MAM and Ig domains of PCP-2 are capable of mediating weak cell-cell adhesion when swapped into the wild-type PTPrho protein, demonstrating that the MAM and Ig domain can mediate weak cell adhesion, but that they require other functional domains within PTPrho to mediate cell-cell adhesion.<ref name="pmid20521994" />  The Ig domain of the R2B RPTP, PTPmu, is sufficient to mediate bead aggregation in vitro,<ref name="pmid7961788">{{cite journal|vauthors=Brady-Kalnay SM, Tonks NK | title=Identification of the homophilic binding site of the receptor protein tyrosine phosphatase PTP mu | journal=J Biol Chem | year= 1994 | volume= 269 | issue= 45 | pages= 28472–7 | pmid=7961788 | doi=  }}</ref> therefore, it is possible that the PCP-2 constructs used by Cheng and colleagues were able to mediate bead aggregation due to a functional Ig domain in PCP-2.<ref name="pmid20521994" /> A functional Ig domain itself would not be sufficient to mediate cell-cell adhesion, however.  Similar to other subfamily members, PCP-2 does not mediate heterophilic binding between different R2B RPTPs.<ref name="pmid20521994" />
 
== Regulation of cadherin-dependent adhesion ==
 
PCP-2 was localized to cell-cell contact sites using immunohistochemistry, and shown to co-localize with [[E-cadherin]] and catenins.<ref name="pmid9070223" />  PCP-2 was shown to be associated with [[B-catenin]] (β-catenin) in cellular lysates.<ref name="pmid9054423" /><ref name="pmid9070223" />
and to directly bind to β-catenin likely via a sequence in the juxtamembrane domain of PCP-2.<ref name="pmid12501215" /><ref name="pmid15986889">{{cite journal |vauthors=He Y, Yan H, Dong H, Zhang P, Tang L, Qiu X, etal | title=Structural basis of interaction between protein tyrosine phosphatase PCP-2 and beta-catenin | journal=Science China Life Sciences | year= 2005 | volume= 48 | issue= 2 | pages= 163–7 | pmid=15986889 | doi=  10.1007/bf02879669}}</ref>  β-catenin has since been shown to be a substrate of PCP-2.<ref name="pmid12501215" /> PCP-2 phosphatase activity antagonizes β-catenin mediated transcription.<ref name="pmid16574648">{{cite journal |vauthors=Yan HX, Yang W, Zhang R, Chen L, Tang L, Zhai B, etal | title=Protein-tyrosine phosphatase PCP-2 inhibits beta-catenin signaling and increases E-cadherin-dependent cell adhesion | journal=J Biol Chem | year= 2006 | volume= 281 | issue= 22 | pages= 15423–33 | pmid=16574648 | doi=10.1074/jbc.M602607200 }}</ref>  A consequence of PCP-2 dephosphorylation of β-catenin is to promote E-cadherin mediated cell-cell adhesion, reduce cellular migration,<ref name="pmid12501215" /> and to reduce cell growth and transformation.<ref name="pmid16574648" />
 
== Role in development ==
 
=== Tissue distribution ===
 
PCP-2 is expressed in the developing mouse nervous system.  In specific, it is expressed in the roof plate and floor plate of the developing spinal cord between embryonic days (E) 10.5 and 13.5.<ref name="pmid8989520">{{cite journal|vauthors=Sommer L, Rao M, Anderson DJ | title=RPTP delta and the novel protein tyrosine phosphatase RPTP psi are expressed in restricted regions of the developing central nervous system | journal=Dev Dyn | year= 1997 | volume= 208 | issue= 1 | pages= 48–61 | pmid=8989520 | doi=10.1002/(SICI)1097-0177(199701)208:1<48::AID-AJA5>3.0.CO;2-1  }}</ref>  At the same developmental time, it is expressed in the ventricular zone in the telecephalon and hindbrain.<ref name="pmid8989520" /><ref name="pmid9510027">{{cite journal|vauthors=Fuchs M, Wang H, Ciossek T, Chen Z, Ullrich A | title=Differential expression of MAM-subfamily protein tyrosine phosphatases during mouse development | journal=Mech Dev | year= 1998 | volume= 70 | issue= 1–2 | pages= 91–109 | pmid=9510027 | doi= 10.1016/S0925-4773(97)00179-2 }}</ref>  PCP-2 was also detected in the developing inner nuclear layer of the retina, in the olfactory epithelium of the nasal cavities, and in the meningeal coverings of the brain.<ref name="pmid9510027" />  In the developing chick nervous system, PCP-2 mRNA is expressed in the ventral midline of the neural tube and in the border between the midbrain and hindbrain, known as the mid-hindbrain boundary.<ref name="pmid12799079" /><ref name="pmid15922674">{{cite journal|vauthors=Badde A, Bumsted-O'Brien KM, Schulte D | title=Chick receptor protein tyrosine phosphatase lambda/psi (cRPTPlambda/cRPTPpsi) is dynamically expressed at the midbrain-hindbrain boundary and in the embryonic neural retina | journal=Gene Expr Patterns | year= 2005 | volume= 5 | issue= 6 | pages= 786–91 | pmid=15922674 | doi=10.1016/j.modgep.2005.04.002 }}</ref>  PCP-2 mRNA is also observed in the ventricular zone of the developing chick neural retina.<ref name="pmid15922674" />
 
PCP-2 is expressed in non-neural tissues during development, including the first forming somite in chick, known as S2,<ref name="pmid12799079" /> the lens fiber cells of the eye, in the esophagus, scleretome, kidneys, lungs, enamel organs (early incisor and molar teeth), and the cochlear ducts of the inner ear.<ref name="pmid8989520" /><ref name="pmid9510027" />  PCP-2 expression in most of these tissue changes over the course of development.<ref name="pmid9510027" />
 
PCP-2 is expressed in meso-diencephalic dopamine (mdDA) neurons<ref name="pmid19515692">{{cite journal |vauthors=Jacobs FM, van der Linden AJ, Wang Y, von Oerthel L, Sul HS, Burbach JP, etal | title=Identification of Dlk1, Ptpru and Klhl1 as novel Nurr1 target genes in meso-diencephalic dopamine neurons | journal=Development | year= 2009 | volume= 136 | issue= 14 | pages= 2363–73 | pmid=19515692 | doi=10.1242/dev.037556 | pmc=3266485  }}</ref>
.  Its expression here is regulated by the coordinated activity of the orphan nuclear receptor [[Nurr1]] binding to the PCP-2 promoter along with the homeobox transcription factor [[Pitx3]].<ref name="pmid19515692" />  Both Nurr1 and Pitx3 are required for the development of mdDA neurons in the brain.  This suggests that PCP-2 is also an important downstream gene for the development of mdDA neurons.<ref name="pmid19515692" />
 
=== Function ===
 
Using morpholinos to reduce PCP-2 (PTP psi) protein expression in zebrafish embryos, Aerne and Ish-Horowicz demonstrated that PCP-2 was required for somite, or body segment, formation during zebrafish development.<ref name="pmid15226256">{{cite journal|vauthors=Aerne B, Ish-Horowicz D | title=Receptor tyrosine phosphatase psi is required for Delta/Notch signalling and cyclic gene expression in the presomitic mesoderm | journal=Development | year= 2004 | volume= 131 | issue= 14 | pages= 3391–9 | pmid=15226256 | doi=10.1242/dev.01222 }}</ref>  Reduction of PCP-2 expression resulted in the loss of boundaries between somites, shortening of the body axis, and disruption of anteroposterior polarity within developing somites. Ultimately, PCP-2 was shown to reduce the expression of the somitogenesis clock genes her1, her7 and delta C, suggesting to the authors that PCP-2 is involved either upstream or in parallel with the Notch-delta signaling pathway during zebrafish development.<ref name="pmid15226256" />
 
PCP-2 is expressed in megakaryocytic cell lines.<ref name="pmid10397721">{{cite journal|vauthors=Taniguchi Y, London R, Schinkmann K, Jiang S, Avraham H | title=The receptor protein tyrosine phosphatase, PTP-RO, is upregulated during megakaryocyte differentiation and Is associated with the c-Kit receptor | journal=Blood | year= 1999 | volume= 94 | issue= 2 | pages= 539–49 | pmid=10397721 | doi= }}</ref>  PCP-2 protein expression in these cell lines is increased by PMA stimulation.<ref name="pmid10397721" />  PCP-2 and the c-Kit tyrosine kinase receptor interact constitutively in these cells, and PCP-2 was shown to be tyrosine phosphorylated upon stimulation with the c-Kit ligand, SCF.<ref name="pmid10397721" />  Antisense oligonucleotide treatment of megakaryocyte cells to reduce PCP-2 protein expression resulted in a significant reduction in megakaryocyte progenitor proliferation.<ref name="pmid10397721" />
 
== Role in cancer ==
PCP-2 is predicted to be a [[tumor suppressor gene]] because of its reduced expression in [[melanoma]] tissue and cell lines.<ref name="pmid11710941">{{cite journal |vauthors=McArdle L, Rafferty M, Maelandsmo GM, Bergin O, Farr CJ, Dervan PA, etal | title=Protein tyrosine phosphatase genes downregulated in melanoma | journal=J Invest Dermatol | year= 2001 | volume= 117 | issue= 5 | pages= 1255–60 | pmid=11710941 | doi=10.1046/j.0022-202x.2001.01534.x }}</ref>
 
==Interactions==
PCP-2 interacts with the following proteins:
* [[β-catenin]]<ref name="pmid9070223" /><ref name="pmid12501215" /><ref name="pmid15986889" />
* Adaptor protein-3 (AP3; [[AP3B1]], [[AP3B2]], [[AP3D1]], [[AP3M1]], [[AP3S1]], [[AP3S2]])<ref name="pmid17622474">{{cite journal|vauthors=Dong H, Yuan H, Jin W, Shen Y, Xu X, Wang H | title=Involvement of beta3A subunit of adaptor protein-3 in intracellular trafficking of receptor-like protein tyrosine phosphatase PCP-2 | journal=Acta Biochim Biophys Sin (Shanghai) | year= 2007 | volume= 39 | issue= 7 | pages= 540–6 | pmid=17622474 | doi= 10.1111/j.1745-7270.2007.00303.x }}</ref>
* Sorting nexin 3 ([[SNX3]])<ref name="pmid17622474" />
* [[C-Kit]] receptor<ref name="pmid10397721" />


==References==
==References==
{{reflist|2}}
{{reflist|35em}}
==Further reading==
 
{{refbegin | 2}}
==External links==
{{PBB_Further_reading
* {{UCSC genome browser|PTPRU}}
| citations =
* {{UCSC gene details|PTPRU}}
*{{cite journal  | author=Wang H, Lian Z, Lerch MM, ''et al.'' |title=Characterization of PCP-2, a novel receptor protein tyrosine phosphatase of the MAM domain family. |journal=Oncogene |volume=12 |issue= 12 |pages= 2555-62 |year= 1996 |pmid= 8700514 |doi=  }}
*{{cite journal  | author=Crossland S, Smith PD, Crompton MR |title=Molecular cloning and characterization of PTP pi, a novel receptor-like protein-tyrosine phosphatase. |journal=Biochem. J. |volume=319 ( Pt 1) |issue=  |pages= 249-54 |year= 1996 |pmid= 8870675 |doi=  }}
*{{cite journal  | author=Bonaldo MF, Lennon G, Soares MB |title=Normalization and subtraction: two approaches to facilitate gene discovery. |journal=Genome Res. |volume=6 |issue= 9 |pages= 791-806 |year= 1997 |pmid= 8889548 |doi=  }}
*{{cite journal  | author=Wang B, Kishihara K, Zhang D, ''et al.'' |title=Molecular cloning and characterization of a novel human receptor protein tyrosine phosphatase gene, hPTP-J: down-regulation of gene expression by PMA and calcium ionophore in Jurkat T lymphoma cells. |journal=Biochem. Biophys. Res. Commun. |volume=231 |issue= 1 |pages= 77-81 |year= 1997 |pmid= 9070223 |doi= 10.1006/bbrc.1997.6004 }}
*{{cite journal  | author=Lin BZ, Pilch PF, Kandror KV |title=Sortilin is a major protein component of Glut4-containing vesicles. |journal=J. Biol. Chem. |volume=272 |issue= 39 |pages= 24145-7 |year= 1997 |pmid= 9305862 |doi=  }}
*{{cite journal  | author=Avraham S, London R, Tulloch GA, ''et al.'' |title=Characterization and chromosomal localization of PTPRO, a novel receptor protein tyrosine phosphatase, expressed in hematopoietic stem cells. |journal=Gene |volume=204 |issue= 1-2 |pages= 5-16 |year= 1998 |pmid= 9434160 |doi=  }}
*{{cite journal  | author=Serra-Pagès C, Medley QG, Tang M, ''et al.'' |title=Liprins, a family of LAR transmembrane protein-tyrosine phosphatase-interacting proteins. |journal=J. Biol. Chem. |volume=273 |issue= 25 |pages= 15611-20 |year= 1998 |pmid= 9624153 |doi= }}
*{{cite journal  | author=Luo Y, Denker BM |title=Interaction of heterotrimeric G protein Galphao with Purkinje cell protein-2. Evidence for a novel nucleotide exchange factor. |journal=J. Biol. Chem. |volume=274 |issue= 16 |pages= 10685-8 |year= 1999 |pmid= 10196137 |doi=  }}
*{{cite journal  | author=Wang B, Kishihara K, Zhang D, ''et al.'' |title=Transcriptional regulation of a receptor protein tyrosine phosphatase gene hPTP-J by PKC-mediated signaling pathways in Jurkat and Molt-4 T lymphoma cells. |journal=Biochim. Biophys. Acta |volume=1450 |issue= 3 |pages= 331-40 |year= 1999 |pmid= 10395944 |doi=  }}
*{{cite journal  | author=Taniguchi Y, London R, Schinkmann K, ''et al.'' |title=The receptor protein tyrosine phosphatase, PTP-RO, is upregulated during megakaryocyte differentiation and Is associated with the c-Kit receptor. |journal=Blood |volume=94 |issue= 2 |pages= 539-49 |year= 1999 |pmid= 10397721 |doi=  }}
*{{cite journal  | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899-903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 }}
*{{cite journal  | author=Yan HX, He YQ, Dong H, ''et al.'' |title=Physical and functional interaction between receptor-like protein tyrosine phosphatase PCP-2 and beta-catenin. |journal=Biochemistry |volume=41 |issue= 52 |pages= 15854-60 |year= 2003 |pmid= 12501215 |doi=  }}
*{{cite journal  | author=Amoui M, Baylink DJ, Tillman JB, Lau KH |title=Expression of a structurally unique osteoclastic protein-tyrosine phosphatase is driven by an alternative intronic, cell type-specific promoter. |journal=J. Biol. Chem. |volume=278 |issue= 45 |pages= 44273-80 |year= 2004 |pmid= 12949066 |doi= 10.1074/jbc.M303933200 }}
*{{cite journal  | author=Ota T, Suzuki Y, Nishikawa T, ''et al.'' |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40-5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
*{{cite journal  | author=Brandenberger R, Wei H, Zhang S, ''et al.'' |title=Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation. |journal=Nat. Biotechnol. |volume=22 |issue= 6 |pages= 707-16 |year= 2005 |pmid= 15146197 |doi= 10.1038/nbt971 }}
*{{cite journal  | author=Willard FS, McCudden CR, Siderovski DP |title=G-protein alpha subunit interaction and guanine nucleotide dissociation inhibitor activity of the dual GoLoco motif protein PCP-2 (Purkinje cell protein-2). |journal=Cell. Signal. |volume=18 |issue= 8 |pages= 1226-34 |year= 2006 |pmid= 16298104 |doi= 10.1016/j.cellsig.2005.10.003 }}
*{{cite journal  | author=Hirakawa M, Tsuruya K, Yotsueda H, ''et al.'' |title=Expression of synaptopodin and GLEPP1 as markers of steroid responsiveness in primary focal segmental glomerulosclerosis. |journal=Life Sci. |volume=79 |issue= 8 |pages= 757-63 |year= 2006 |pmid= 16564554 |doi= 10.1016/j.lfs.2006.02.031 }}
*{{cite journal  | author=Yan HX, Yang W, Zhang R, ''et al.'' |title=Protein-tyrosine phosphatase PCP-2 inhibits beta-catenin signaling and increases E-cadherin-dependent cell adhesion. |journal=J. Biol. Chem. |volume=281 |issue= 22 |pages= 15423-33 |year= 2006 |pmid= 16574648 |doi= 10.1074/jbc.M602607200 }}
}}
{{refend}}


{{protein-stub}}
{{Protein tyrosine phosphatases}}
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Latest revision as of 18:59, 7 September 2017

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Identifiers
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Orthologs
SpeciesHumanMouse
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Receptor-type tyrosine-protein phosphatase PCP-2 (also known as PTP-pi, PTP lambda, hPTP-J, PTPRO and PTP psi), is an enzyme that in humans is encoded by the PTPRU gene.[1][2][3]

Function

The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and two tandem intracellular catalytic tyrosine phosphatase domains, and thus represents a receptor-type PTP (RPTP). The extracellular region contains a meprin-A5 antigen-PTPmu (MAM) domain, one Ig-like domain and four fibronectin type III-like repeats, and thus is a member of the type R2B RPTP family. It was cloned by many groups and given different names, including PCP-2,[1] PTP pi,[4] PTP lambda,[5] hPTP-J,[6] PTPRO,[2] and PTP psi.[7] Other type R2B RPTPs include PTPRM, PTPRK, and PTPRT. Analysis of the genomic structure of PCP-2 suggests that it is the most distantly related of the type R2B RPTPS.[8]

RPTPs are able to remove phosphate moieties from tyrosine residues. Although the R2B family of RPTPs are characterized as having two tyrosine phosphatase domains in their intracellular domain, usually only one is catalytically active.[9][10] A point mutation study suggests that only the first phosphatase domain of PCP-2 is catalytically active and able to dephosphorylate β-catenin.[11] A recombinant protein with both PCP-2 phosphatase domains was also able to dephosphorylate EGFR.[4] However, when each of the two intracellular catalytic tyrosine phosphatase domains are expressed individually as recombinant proteins and assayed in vitro using the artificial substrate ρ-nitrophenol phosphate (pNPP), both the first and second intracellular tyrosine phosphatase domain were able to dephosphorylate pNPP.[4]

Regulation

PCP-2 mRNA is regulated by phorbol myristate acetate (PMA) or calcium ionophore, okadaic acid, the Ras inhibitor manumycin, and orthovanadate in Jurkat T lymphoma cells.[6][12]

Alternative splicing

Four alternatively spliced transcript variants, which encode distinct proteins, have been reported.[3]

Examination of mouse full-length cDNA sequences for alternatively spliced phosphatase genes identified two novel forms of PTPRU predicted to result in two PCP-2 splice variants: a tethered variant of PCP-2, expressing an intact extracellular and transmembrane domain, and a PCP-2 variant that lacked a signal peptide, but encoded intact transmembrane and cytoplasmic domains.[13]

Homophilic binding

The MAM, Ig and first fibronectin III domain of PCP-2 was shown to mediate bead aggregation in vitro.[5] PCP-2 accomplishes this by binding to another PCP-2 molecule on a fluorescent bead, known as homophilic binding. PCP-2 was unable to mediate aggregation between non-adherent cells when expressed as a full-length protein, however, suggesting that PCP-2 does not mediate homophilic adhesion in cells.[14] The MAM and Ig domains of PCP-2 are capable of mediating weak cell-cell adhesion when swapped into the wild-type PTPrho protein, demonstrating that the MAM and Ig domain can mediate weak cell adhesion, but that they require other functional domains within PTPrho to mediate cell-cell adhesion.[14] The Ig domain of the R2B RPTP, PTPmu, is sufficient to mediate bead aggregation in vitro,[15] therefore, it is possible that the PCP-2 constructs used by Cheng and colleagues were able to mediate bead aggregation due to a functional Ig domain in PCP-2.[14] A functional Ig domain itself would not be sufficient to mediate cell-cell adhesion, however. Similar to other subfamily members, PCP-2 does not mediate heterophilic binding between different R2B RPTPs.[14]

Regulation of cadherin-dependent adhesion

PCP-2 was localized to cell-cell contact sites using immunohistochemistry, and shown to co-localize with E-cadherin and catenins.[6] PCP-2 was shown to be associated with B-catenin (β-catenin) in cellular lysates.[5][6] and to directly bind to β-catenin likely via a sequence in the juxtamembrane domain of PCP-2.[11][16] β-catenin has since been shown to be a substrate of PCP-2.[11] PCP-2 phosphatase activity antagonizes β-catenin mediated transcription.[17] A consequence of PCP-2 dephosphorylation of β-catenin is to promote E-cadherin mediated cell-cell adhesion, reduce cellular migration,[11] and to reduce cell growth and transformation.[17]

Role in development

Tissue distribution

PCP-2 is expressed in the developing mouse nervous system. In specific, it is expressed in the roof plate and floor plate of the developing spinal cord between embryonic days (E) 10.5 and 13.5.[18] At the same developmental time, it is expressed in the ventricular zone in the telecephalon and hindbrain.[18][19] PCP-2 was also detected in the developing inner nuclear layer of the retina, in the olfactory epithelium of the nasal cavities, and in the meningeal coverings of the brain.[19] In the developing chick nervous system, PCP-2 mRNA is expressed in the ventral midline of the neural tube and in the border between the midbrain and hindbrain, known as the mid-hindbrain boundary.[7][20] PCP-2 mRNA is also observed in the ventricular zone of the developing chick neural retina.[20]

PCP-2 is expressed in non-neural tissues during development, including the first forming somite in chick, known as S2,[7] the lens fiber cells of the eye, in the esophagus, scleretome, kidneys, lungs, enamel organs (early incisor and molar teeth), and the cochlear ducts of the inner ear.[18][19] PCP-2 expression in most of these tissue changes over the course of development.[19]

PCP-2 is expressed in meso-diencephalic dopamine (mdDA) neurons[21] . Its expression here is regulated by the coordinated activity of the orphan nuclear receptor Nurr1 binding to the PCP-2 promoter along with the homeobox transcription factor Pitx3.[21] Both Nurr1 and Pitx3 are required for the development of mdDA neurons in the brain. This suggests that PCP-2 is also an important downstream gene for the development of mdDA neurons.[21]

Function

Using morpholinos to reduce PCP-2 (PTP psi) protein expression in zebrafish embryos, Aerne and Ish-Horowicz demonstrated that PCP-2 was required for somite, or body segment, formation during zebrafish development.[22] Reduction of PCP-2 expression resulted in the loss of boundaries between somites, shortening of the body axis, and disruption of anteroposterior polarity within developing somites. Ultimately, PCP-2 was shown to reduce the expression of the somitogenesis clock genes her1, her7 and delta C, suggesting to the authors that PCP-2 is involved either upstream or in parallel with the Notch-delta signaling pathway during zebrafish development.[22]

PCP-2 is expressed in megakaryocytic cell lines.[23] PCP-2 protein expression in these cell lines is increased by PMA stimulation.[23] PCP-2 and the c-Kit tyrosine kinase receptor interact constitutively in these cells, and PCP-2 was shown to be tyrosine phosphorylated upon stimulation with the c-Kit ligand, SCF.[23] Antisense oligonucleotide treatment of megakaryocyte cells to reduce PCP-2 protein expression resulted in a significant reduction in megakaryocyte progenitor proliferation.[23]

Role in cancer

PCP-2 is predicted to be a tumor suppressor gene because of its reduced expression in melanoma tissue and cell lines.[24]

Interactions

PCP-2 interacts with the following proteins:

References

  1. ↑ 1.0 1.1 Wang H, Lian Z, Lerch MM, Chen Z, Xie W, Ullrich A (Sep 1996). "Characterization of PCP-2, a novel receptor protein tyrosine phosphatase of the MAM domain family". Oncogene. 12 (12): 2555–62. PMID 8700514.
  2. ↑ 2.0 2.1 Avraham S, London R, Tulloch GA, Ellis M, Fu Y, Jiang S, White RA, Painter C, Steinberger AA, Avraham H (Feb 1998). "Characterization and chromosomal localization of PTPRO, a novel receptor protein tyrosine phosphatase, expressed in hematopoietic stem cells". Gene. 204 (1–2): 5–16. doi:10.1016/S0378-1119(97)00420-4. PMID 9434160.
  3. ↑ 3.0 3.1 "Entrez Gene: PTPRU protein tyrosine phosphatase, receptor type, U".
  4. ↑ 4.0 4.1 4.2 Crossland S, Smith PD, Crompton MR (1996). "Molecular cloning and characterization of PTP pi, a novel receptor-like protein-tyrosine phosphatase". Biochem J. 319 (1): 249–54. PMC 1217761. PMID 8870675.
  5. ↑ 5.0 5.1 5.2 Cheng J, Wu K, Armanini M, O'Rourke N, Dowbenko D, Lasky LA (1997). "A novel protein-tyrosine phosphatase related to the homotypically adhering kappa and mu receptors". J Biol Chem. 272 (11): 7264–77. doi:10.1074/jbc.272.11.7264. PMID 9054423.
  6. ↑ 6.0 6.1 6.2 6.3 6.4 Wang B, Kishihara K, Zhang D, Hara H, Nomoto K (1997). "Molecular cloning and characterization of a novel human receptor protein tyrosine phosphatase gene, hPTP-J: down-regulation of gene expression by PMA and calcium ionophore in Jurkat T lymphoma cells". Biochem Biophys Res Commun. 231 (1): 77–81. doi:10.1006/bbrc.1997.6004. PMID 9070223.
  7. ↑ 7.0 7.1 7.2 Aerne B, Stoker A, Ish-Horowicz D (2003). "Chick receptor tyrosine phosphatase Psi is dynamically expressed during somitogenesis". Gene Expr Patterns. 3 (3): 325–9. doi:10.1016/S1567-133X(03)00038-3. PMID 12799079.
  8. ↑ Besco J, Popesco MC, Davuluri RV, Frostholm A, Rotter A (2004). "Genomic structure and alternative splicing of murine R2B receptor protein tyrosine phosphatases (PTPkappa, mu, rho and PCP-2)". BMC Genomics. 5 (1): 14. doi:10.1186/1471-2164-5-14. PMC 373446. PMID 15040814.
  9. ↑ Johnson KG, Van Vactor D (2003). "Receptor protein tyrosine phosphatases in nervous system development". Physiol Rev. 83 (1): 1–24. doi:10.1152/physrev.00016.2002. PMID 12506125.
  10. ↑ Ensslen-Craig SE, Brady-Kalnay SM (2004). "Receptor protein tyrosine phosphatases regulate neural development and axon guidance". Dev Biol. 275 (1): 12–22. doi:10.1016/j.ydbio.2004.08.009. PMID 15464569.
  11. ↑ 11.0 11.1 11.2 11.3 11.4 Yan HX, He YQ, Dong H, Zhang P, Zeng JZ, Cao HF, et al. (2002). "Physical and functional interaction between receptor-like protein tyrosine phosphatase PCP-2 and beta-catenin". Biochemistry. 41 (52): 15854–60. doi:10.1021/bi026095u. PMID 12501215.
  12. ↑ Wang B, Kishihara K, Zhang D, Sakamoto T, Nomoto K (1999). "Transcriptional regulation of a receptor protein tyrosine phosphatase gene hPTP-J by PKC-mediated signaling pathways in Jurkat and Molt-4 T lymphoma cells". Biochim Biophys Acta. 1450 (3): 331–40. doi:10.1016/S0167-4889(99)00064-6. PMID 10395944.
  13. ↑ Forrest AR, Taylor DF, Crowe ML, Chalk AM, Waddell NJ, Kolle G, et al. (2006). "Genome-wide review of transcriptional complexity in mouse protein kinases and phosphatases". Genome Biol. 7 (1): R5. doi:10.1186/gb-2006-7-1-r5. PMC 1431701. PMID 16507138.
  14. ↑ 14.0 14.1 14.2 14.3 Becka S, Zhang P, Craig SE, Lodowski DT, Wang Z, Brady-Kalnay SM (2010). "Characterization of the adhesive properties of the type IIb subfamily receptor protein tyrosine phosphatases". Cell Commun Adhes. 17 (2): 34–47. doi:10.3109/15419061.2010.487957. PMC 3337334. PMID 20521994.
  15. ↑ Brady-Kalnay SM, Tonks NK (1994). "Identification of the homophilic binding site of the receptor protein tyrosine phosphatase PTP mu". J Biol Chem. 269 (45): 28472–7. PMID 7961788.
  16. ↑ 16.0 16.1 He Y, Yan H, Dong H, Zhang P, Tang L, Qiu X, et al. (2005). "Structural basis of interaction between protein tyrosine phosphatase PCP-2 and beta-catenin". Science China Life Sciences. 48 (2): 163–7. doi:10.1007/bf02879669. PMID 15986889.
  17. ↑ 17.0 17.1 Yan HX, Yang W, Zhang R, Chen L, Tang L, Zhai B, et al. (2006). "Protein-tyrosine phosphatase PCP-2 inhibits beta-catenin signaling and increases E-cadherin-dependent cell adhesion". J Biol Chem. 281 (22): 15423–33. doi:10.1074/jbc.M602607200. PMID 16574648.
  18. ↑ 18.0 18.1 18.2 Sommer L, Rao M, Anderson DJ (1997). "RPTP delta and the novel protein tyrosine phosphatase RPTP psi are expressed in restricted regions of the developing central nervous system". Dev Dyn. 208 (1): 48–61. doi:10.1002/(SICI)1097-0177(199701)208:1<48::AID-AJA5>3.0.CO;2-1. PMID 8989520.
  19. ↑ 19.0 19.1 19.2 19.3 Fuchs M, Wang H, Ciossek T, Chen Z, Ullrich A (1998). "Differential expression of MAM-subfamily protein tyrosine phosphatases during mouse development". Mech Dev. 70 (1–2): 91–109. doi:10.1016/S0925-4773(97)00179-2. PMID 9510027.
  20. ↑ 20.0 20.1 Badde A, Bumsted-O'Brien KM, Schulte D (2005). "Chick receptor protein tyrosine phosphatase lambda/psi (cRPTPlambda/cRPTPpsi) is dynamically expressed at the midbrain-hindbrain boundary and in the embryonic neural retina". Gene Expr Patterns. 5 (6): 786–91. doi:10.1016/j.modgep.2005.04.002. PMID 15922674.
  21. ↑ 21.0 21.1 21.2 Jacobs FM, van der Linden AJ, Wang Y, von Oerthel L, Sul HS, Burbach JP, et al. (2009). "Identification of Dlk1, Ptpru and Klhl1 as novel Nurr1 target genes in meso-diencephalic dopamine neurons". Development. 136 (14): 2363–73. doi:10.1242/dev.037556. PMC 3266485. PMID 19515692.
  22. ↑ 22.0 22.1 Aerne B, Ish-Horowicz D (2004). "Receptor tyrosine phosphatase psi is required for Delta/Notch signalling and cyclic gene expression in the presomitic mesoderm". Development. 131 (14): 3391–9. doi:10.1242/dev.01222. PMID 15226256.
  23. ↑ 23.0 23.1 23.2 23.3 23.4 Taniguchi Y, London R, Schinkmann K, Jiang S, Avraham H (1999). "The receptor protein tyrosine phosphatase, PTP-RO, is upregulated during megakaryocyte differentiation and Is associated with the c-Kit receptor". Blood. 94 (2): 539–49. PMID 10397721.
  24. ↑ McArdle L, Rafferty M, Maelandsmo GM, Bergin O, Farr CJ, Dervan PA, et al. (2001). "Protein tyrosine phosphatase genes downregulated in melanoma". J Invest Dermatol. 117 (5): 1255–60. doi:10.1046/j.0022-202x.2001.01534.x. PMID 11710941.
  25. ↑ 25.0 25.1 Dong H, Yuan H, Jin W, Shen Y, Xu X, Wang H (2007). "Involvement of beta3A subunit of adaptor protein-3 in intracellular trafficking of receptor-like protein tyrosine phosphatase PCP-2". Acta Biochim Biophys Sin (Shanghai). 39 (7): 540–6. doi:10.1111/j.1745-7270.2007.00303.x. PMID 17622474.

External links

Retrieved from "https://www.wikidoc.org/index.php?title=PTPRU&oldid=1411099"