PTPRU

From Wikipedia, the free encyclopedia
(Redirected from PTPRU (gene))
PTPRU
Identifiers
AliasesPTPRU, FMI, PCP-2, PTP, PTP-J, PTP-PI, PTP-RO, PTPPSI, PTPRO, PTPU2, R-PTP-PSI, R-PTP-U, hPTP-J, protein tyrosine phosphatase, receptor type U, protein tyrosine phosphatase receptor type U
External IDsOMIM: 602454 MGI: 1321151 HomoloGene: 4168 GeneCards: PTPRU
Orthologs
SpeciesHumanMouse
Entrez

10076

19273

Ensembl

ENSG00000060656

ENSMUSG00000028909

UniProt

Q92729

B1AUH1

RefSeq (mRNA)

NM_001195001
NM_005704
NM_133177
NM_133178

NM_001083119
NM_011214

RefSeq (protein)

NP_001181930
NP_005695
NP_573438
NP_573439

NP_001076588
NP_035344

Location (UCSC)Chr 1: 29.24 – 29.33 MbChr 4: 131.77 – 131.84 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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.[5][6][7]

Function[edit]

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,[5] PTP pi,[8] PTP lambda,[9] hPTP-J,[10] PTPRO,[6] and PTP psi.[11] 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.[12]

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.[13][14] A point mutation study suggests that only the first phosphatase domain of PCP-2 is catalytically active and able to dephosphorylate β-catenin.[15] A recombinant protein with both PCP-2 phosphatase domains was also able to dephosphorylate EGFR.[8] 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.[8]

PTPRU as a pseudophosphatase[edit]

The X-ray crystallographic structure of the first PTPRU phopshatase (D1) domain shows that several divergent sequences in key catalytic motifs result in structural rearrangements that render this domain catalytically inactive.[16] Phosphatase activity for the PTPRU D1 phosphatase domain is undetectable against a range of phosphorylated substrates, and the full PTPRU intracellular domain cannot dephosphorylate pNPP, suggesting PTPRU completely lacks phosphatase activity. [16] PTPRU can therefore be classified as a pseudoenzyme, in this case a pseudophosphatase. [17] Despite a lack of catalytic activity, PTPRU is able to bind the substrates of the related RPTP, PTPRK.[16] Removal of PTPRU from MCF10A breast epithelial cells leads to a reduction in phosphorylation of the cell adhesion protein p120-Catenin, suggesting PTPRU binding may act to sequester and protect proteins from dephosphorylation by active phosphatases.[16]

Regulation[edit]

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.[10][18]

Alternative splicing[edit]

Four alternatively spliced transcript variants, which encode distinct proteins, have been reported.[7]

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.[19]

Homophilic binding[edit]

The MAM, Ig and first fibronectin III domain of PCP-2 was shown to mediate bead aggregation in vitro.[9] 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.[20] 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.[20] The Ig domain of the R2B RPTP, PTPmu, is sufficient to mediate bead aggregation in vitro,[21] 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.[20] 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.[20]

Regulation of cadherin-dependent adhesion[edit]

PCP-2 was localized to cell-cell contact sites using immunohistochemistry, and shown to co-localize with E-cadherin and catenins.[10] PCP-2 was shown to be associated with B-catenin (β-catenin) in cellular lysates.[9][10] and to directly bind to β-catenin likely via a sequence in the juxtamembrane domain of PCP-2.[15][22] β-catenin has since been shown to be a substrate of PCP-2.[15] PCP-2 phosphatase activity antagonizes β-catenin mediated transcription.[23] A consequence of PCP-2 dephosphorylation of β-catenin is to promote E-cadherin mediated cell-cell adhesion, reduce cellular migration,[15] and to reduce cell growth and transformation.[23]

Role in development[edit]

Tissue distribution[edit]

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.[24] At the same developmental time, it is expressed in the ventricular zone in the telecephalon and hindbrain.[24][25] 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.[25] 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.[11][26] PCP-2 mRNA is also observed in the ventricular zone of the developing chick neural retina.[26]

PCP-2 is expressed in non-neural tissues during development, including the first forming somite in chick, known as S2,[11] 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.[24][25] PCP-2 expression in most of these tissue changes over the course of development.[25]

PCP-2 is expressed in meso-diencephalic dopamine (mdDA) neurons.[27] 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.[27] 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.[27]

Function[edit]

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.[28] 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.[28]

PCP-2 is expressed in megakaryocytic cell lines.[29] PCP-2 protein expression in these cell lines is increased by PMA stimulation.[29] 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.[29] Antisense oligonucleotide treatment of megakaryocyte cells to reduce PCP-2 protein expression resulted in a significant reduction in megakaryocyte progenitor proliferation.[29]

Role in cancer[edit]

PCP-2 is predicted to be a tumor suppressor gene because of its reduced expression in melanoma tissue and cell lines.[30]

Interactions[edit]

PCP-2 interacts with the following proteins:

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000060656 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000028909 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b 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.
  6. ^ a b 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.
  7. ^ a b "Entrez Gene: PTPRU protein tyrosine phosphatase, receptor type, U".
  8. ^ a b c 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. doi:10.1042/bj3190249. PMC 1217761. PMID 8870675.
  9. ^ a b c 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.
  10. ^ a b c d e 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.
  11. ^ a b c 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.
  12. ^ 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.
  13. ^ 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.
  14. ^ 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.
  15. ^ a b c d e 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.
  16. ^ a b c d Hay IM, Fearnley GW, Rios P, Köhn M, Sharpe HJ, Deane JE (June 2020). "The receptor PTPRU is a redox sensitive pseudophosphatase". Nature Communications. 11 (1): 3219. Bibcode:2020NatCo..11.3219H. doi:10.1038/s41467-020-17076-w. PMC 7320164. PMID 32591542.
  17. ^ Reiterer V, Pawłowski K, Desrochers G, Pause A, Sharpe HJ, Farhan H (October 2020). "The dead phosphatases society: a review of the emerging roles of pseudophosphatases". The FEBS Journal. 287 (19): 4198–4220. doi:10.1111/febs.15431. hdl:10852/85557. PMID 32484316. S2CID 219168614.
  18. ^ 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.
  19. ^ 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.
  20. ^ a b c d 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.
  21. ^ 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. doi:10.1016/S0021-9258(18)46951-7. PMID 7961788.
  22. ^ a b 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. S2CID 20799629.
  23. ^ a b 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.
  24. ^ a b c 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.
  25. ^ a b c d 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. S2CID 9560178.
  26. ^ a b 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.
  27. ^ a b c 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.
  28. ^ a b 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. S2CID 9827113.
  29. ^ a b c d e 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. doi:10.1182/blood.V94.2.539. PMID 10397721.
  30. ^ 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.
  31. ^ a b 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. S2CID 27621318.

External links[edit]

Retrieved from "https://en.wikipedia.org/w/index.php?title=PTPRU&oldid=1192153648"