Molecular cloning and chromosomal localization of a human gene homologous to the murine R-PTP-k, a receptor-type protein tyrosine phosphatase

Cited 26 time in scopus
Metadata Downloads

Full metadata record

DC FieldValueLanguage
dc.contributor.authorYoung Yang-
dc.contributor.authorMin Chan Gil-
dc.contributor.authorEun Young Choi-
dc.contributor.authorSeong Hoe Park-
dc.contributor.authorKwang Ho Pyun-
dc.contributor.authorHyun Jung Ha-
dc.date.accessioned2017-04-19T08:56:13Z-
dc.date.available2017-04-19T08:56:13Z-
dc.date.issued1997-
dc.identifier.issn0378-1119-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/4766-
dc.description.abstractTyrosine phosphorylation of proteins plays an important role in cellular signaling and many cellular activities. The levels of cellular phosphorylation are reversibly controlled by protein tyrosine kinases and protein tyrosine phosphatases. The murine R-PTP-κ, a receptor-type protein tyrosine phosphatase, has recently been cloned. In order to identify the protein tyrosine phosphatases critical to the cellular signal transduction in human keratinocytes, a polymerase chain reaction (PCR)-based strategy was employed, and we have cloned a human homologue of the murine R-PTP-κ. Here, we report the isolation of a complementary DNA encoding a human R-PTP-κ. of the several overlapping cDNA clones, one clone, which we originally termed p55-7, was found to encode a transmembrane protein of 1440 amino acids and was highly conserved with murine R-PTP-κ with 98% identity at the amino-acid levels. The human R-PTP-κ gene was localized to chromosome 6 by southern hybridization of DNA from a rodent/human somatic cell mapping panel. Northern blot analysis of RNA from several human tissues revealed, like the murine R-PTP-κ, the presence of a major mRNA of approx. 7.0 kb and a minor mRNA of approx. 5.3 kb. In contrast to the expression of murine R-PTP-κ which was highly expressed in liver and kidney, the human R-PTP-κ was predominantly expressed in spleen, prostate, and ovary. However, the transcripts were detectable at various levels in all examined tissues (thymus, testis, small intestine, and colon) except for PBL (peripheral blood leukocytes). In addition, human R-PTP-κ displayed a restricted pattern of expression among a series of cell lines, and was apparently expressed in an epidermal cells and cell lines (human normal keratinocytes, HaCaT, and A431), but was not detectable in other cell lines tested after longer exposure.-
dc.publisherElsevier-
dc.titleMolecular cloning and chromosomal localization of a human gene homologous to the murine R-PTP-k, a receptor-type protein tyrosine phosphatase-
dc.title.alternativeMolecular cloning and chromosomal localization of a human gene homologous to the murine R-PTP-k, a receptor-type protein tyrosine phosphatase-
dc.typeArticle-
dc.citation.titleGene-
dc.citation.number0-
dc.citation.endPage82-
dc.citation.startPage77-
dc.citation.volume186-
dc.contributor.affiliatedAuthorYoung Yang-
dc.contributor.affiliatedAuthorMin Chan Gil-
dc.contributor.affiliatedAuthorKwang Ho Pyun-
dc.contributor.alternativeName양영-
dc.contributor.alternativeName길민찬-
dc.contributor.alternativeName최은영-
dc.contributor.alternativeName박성혜-
dc.contributor.alternativeName변광호-
dc.contributor.alternativeName하현정-
dc.identifier.bibliographicCitationGene, vol. 186, pp. 77-82-
dc.identifier.doi10.1016/S0378-1119(96)00684-1-
dc.subject.keywordRecombinant DNA-
dc.subject.keywordHuman R-PTP-κ-
dc.subject.keywordGene expression-
dc.subject.keywordHuman keratinocytes-
dc.subject.localrecombinant DNA-
dc.subject.localRecombinant DNA-
dc.subject.localHuman R-PTP-κ-
dc.subject.localGene Expression-
dc.subject.localGene expression-
dc.subject.localgene expression-
dc.subject.localHuman keratinocytes-
dc.description.journalClassY-
Appears in Collections:
1. Journal Articles > Journal Articles
Files in This Item:
  • There are no files associated with this item.


Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.