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Identification and characterization of a truncated isoform of NELL2

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dc.contributor.authorKim, Dong-Gyu-
dc.contributor.authorHwang, Eun Mi-
dc.contributor.authorYoo, Jae Cheal-
dc.contributor.authorKim, Eunju-
dc.contributor.authorPark, Nammi-
dc.contributor.authorRhee, Sangmyung-
dc.contributor.authorHa, Chang Man-
dc.contributor.authorHong, Seong-Geun-
dc.contributor.authorPark, Jae-Yong-
dc.date.accessioned2022-12-27T04:21:32Z-
dc.date.available2022-12-27T04:21:32Z-
dc.date.issued2010-01-01-
dc.identifier.issn0006-291X-
dc.identifier.issn1090-2104-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/25256-
dc.description.abstractNELL2 is a neuron-specific secreted glycoprotein containing in N-terminal thrombospondin I-like domain (TSP-N) In this study. we describe NELL2-Tsp, a novel alternative splice variant of rat NELL2 NELL2-Tsp uses an alternate stop codon resulting in a C-terminal truncated form of NELL2, containing a signal peptide and a TSP-N domain NELL2-Tsp is a glycosylated protein specifically expressed In brain tissue. NELL2-Tsp and NELL2 are secreted, likely due to the putative signal peptide. However. Clue to the truncation, the secreted portion of NELL2-Tsp is smaller than that of NELL2 Immunoprecipitation analysis confirmed that NELL2-Tsp was able to associate with NELL2 and with itself In addition, expression of NELL2-Tsp notably reduced secretion of NELL2 and inhibited NELL2-mediated neurite Outgrowth These results suggest that NELL2-Tsp may act as a negative regulator of wild-type NELL2 (C) 2009 Elsevier Inc All rights reserved-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleIdentification and characterization of a truncated isoform of NELL2-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.bbrc.2009.11.092-
dc.identifier.wosid000273624500093-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.391, no.1, pp 529 - 534-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume391-
dc.citation.number1-
dc.citation.startPage529-
dc.citation.endPage534-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusDOMAIN-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusNEURONS-
dc.subject.keywordAuthorNELL2-
dc.subject.keywordAuthorTruncated NELL2-
dc.subject.keywordAuthorAlternative splicing-
dc.subject.keywordAuthorNeurite outgrowth-
dc.subject.keywordAuthorSecretion-
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