Protein tyrosine phosphatase profiling analysis of HIB-1B cells during brown adipogenesis

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dc.contributor.authorHye-Ryung Choi-
dc.contributor.authorWon Kon Kim-
dc.contributor.authorEun Young Kim-
dc.contributor.authorHyeyun Jung-
dc.contributor.authorJeong Hoon Kim-
dc.contributor.authorBaek Soo Han-
dc.contributor.authorK H You-
dc.contributor.authorSang Chul Lee-
dc.contributor.authorKwang-Hee Bae-
dc.date.accessioned2017-04-19T09:30:02Z-
dc.date.available2017-04-19T09:30:02Z-
dc.date.issued2012-
dc.identifier.issn1017-7825-
dc.identifier.uri10.4014/jmb.1112.12059ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/10713-
dc.description.abstractA number of evidence have been accumulated that the regulation of reversible tyrosine phosphorylation, which can be regulated by the combinatorial activity of protein tyrosine kinases (PTKs) and protein tyrosine phosphatases (PTPs), plays crucial roles in various biological processes including differentiation. There are a total of 107 PTP genes in the human genome, collectively referred to as the "PTPome." In this study, we performed PTP profiling analysis of the HIB-1B cell line, a brown preadipocyte cell line, during brown adipogenesis. Through RT-PCR and real-time PCR, several PTPs showing differential expression pattern during brown adipogenesis were identified. In the case of PTP-RE, it was shown to decrease significantly until 4 days after brown adipogenic differentiation, followed by a dramatic increase at 6 days. The overexpression of PTP-RE led to decreased brown adipogenic differentiation via reducing the tyrosine phosphorylation of the insulin receptor, indicating that PTP-RE functions as a negative regulator at the early stage of brown adipogenesis.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titleProtein tyrosine phosphatase profiling analysis of HIB-1B cells during brown adipogenesis-
dc.title.alternativeProtein tyrosine phosphatase profiling analysis of HIB-1B cells during brown adipogenesis-
dc.typeArticle-
dc.citation.titleJournal of Microbiology and Biotechnology-
dc.citation.number7-
dc.citation.endPage1033-
dc.citation.startPage1029-
dc.citation.volume22-
dc.contributor.affiliatedAuthorHye-Ryung Choi-
dc.contributor.affiliatedAuthorWon Kon Kim-
dc.contributor.affiliatedAuthorEun Young Kim-
dc.contributor.affiliatedAuthorHyeyun Jung-
dc.contributor.affiliatedAuthorJeong Hoon Kim-
dc.contributor.affiliatedAuthorBaek Soo Han-
dc.contributor.affiliatedAuthorSang Chul Lee-
dc.contributor.affiliatedAuthorKwang-Hee Bae-
dc.contributor.alternativeName최혜령-
dc.contributor.alternativeName김원곤-
dc.contributor.alternativeName김은영-
dc.contributor.alternativeName정혜윤-
dc.contributor.alternativeName김정훈-
dc.contributor.alternativeName한백수-
dc.contributor.alternativeName유관희-
dc.contributor.alternativeName이상철-
dc.contributor.alternativeName배광희-
dc.identifier.bibliographicCitationJournal of Microbiology and Biotechnology, vol. 22, no. 7, pp. 1029-1033-
dc.identifier.doi10.4014/jmb.1112.12059-
dc.subject.keywordBrown adipogenesis-
dc.subject.keywordProtein tyrosine phosphatase-
dc.subject.keywordPTP-RE-
dc.subject.keywordPTPome-
dc.subject.localBrown adipogenesis-
dc.subject.localbrown adipogenesis-
dc.subject.localProtein tyrosine phosphatases-
dc.subject.localProtein tyrosine phosphatase-
dc.subject.localprotein tyrosine phosphatase-
dc.subject.localPTP-RE-
dc.subject.localPTPome-
dc.description.journalClassY-
Appears in Collections:
Division of A.I. & Biomedical Research > Metabolic Regulation Research Center > 1. Journal Articles
Division of A.I. & Biomedical Research > Orphan Disease Therapeutic Target Research Center > 1. Journal Articles
Division of Research on National Challenges > Biodefense Research Center > 1. Journal Articles
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