Cited 6 time in
Kaposi's sarcoma-associated herpesvirus viral protein kinase phosphorylates extracellular signal-regulated kinase and activates MAPK/ERK signaling pathway
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kim, Hyungdong | - |
| dc.contributor.author | Jang, Jun Hyeong | - |
| dc.contributor.author | Song, Yul Eum | - |
| dc.contributor.author | Seo, Taegun | - |
| dc.date.accessioned | 2023-04-28T00:40:54Z | - |
| dc.date.available | 2023-04-28T00:40:54Z | - |
| dc.date.issued | 2020-01-22 | - |
| dc.identifier.issn | 0006-291X | - |
| dc.identifier.issn | 1090-2104 | - |
| dc.identifier.uri | https://scholarworks.dongguk.edu/handle/sw.dongguk/6996 | - |
| dc.description.abstract | Open reading frame 36 (ORF36) of Kaposi's sarcoma-associated herpesvirus (KSHV) encodes a serine/threonine-type viral protein kinase (vPK). Previous studies have examined the functions of KSHV vPK; however, its role in the activation of extracellular signal-regulated kinase (ERK1/2) has not yet been described to date. Using HEK 293 cell lines, we performed a human phospho-kinase array analysis to screen for MAPK signaling pathways kinases that are activated by KSHV vPK. In addition, we investigated the regulator protein phosphorylation of up/downstream ERK1/2 pathway; nuclear translocation of phosphorylated ERK1/2; and regulation of transcription factor, inflammatory cytokine, and pro-/antiapoptotic factor by KSHV vPK transfection. Here, we demonstrated that KSHV vPK activates ERK1/2 signaling pathway and plays an important role in the activation of MAPK/ERK signaling pathway. (C) 2019 Elsevier Inc. All rights reserved. | - |
| dc.format.extent | 6 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | ACADEMIC PRESS INC ELSEVIER SCIENCE | - |
| dc.title | Kaposi's sarcoma-associated herpesvirus viral protein kinase phosphorylates extracellular signal-regulated kinase and activates MAPK/ERK signaling pathway | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1016/j.bbrc.2019.11.038 | - |
| dc.identifier.scopusid | 2-s2.0-85075401573 | - |
| dc.identifier.wosid | 000507487200041 | - |
| dc.identifier.bibliographicCitation | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.521, no.4, pp 1083 - 1088 | - |
| dc.citation.title | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | - |
| dc.citation.volume | 521 | - |
| dc.citation.number | 4 | - |
| dc.citation.startPage | 1083 | - |
| dc.citation.endPage | 1088 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
| dc.relation.journalResearchArea | Biophysics | - |
| dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
| dc.relation.journalWebOfScienceCategory | Biophysics | - |
| dc.subject.keywordPlus | GROWTH-FACTOR RECEPTOR | - |
| dc.subject.keywordPlus | NUCLEAR TRANSLOCATION | - |
| dc.subject.keywordPlus | DNA-SEQUENCES | - |
| dc.subject.keywordPlus | RAS/RAF/MEK/ERK PATHWAY | - |
| dc.subject.keywordPlus | TRANSCRIPTION FACTORS | - |
| dc.subject.keywordPlus | C-MYC | - |
| dc.subject.keywordPlus | ERK | - |
| dc.subject.keywordPlus | EXPRESSION | - |
| dc.subject.keywordPlus | LOCALIZATION | - |
| dc.subject.keywordPlus | TRANSDUCTION | - |
| dc.subject.keywordAuthor | KSHV | - |
| dc.subject.keywordAuthor | Viral protein kinase | - |
| dc.subject.keywordAuthor | ORF36 | - |
| dc.subject.keywordAuthor | MAPK/ERK signaling pathway | - |
| dc.subject.keywordAuthor | ERK | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
30, Pildong-ro 1-gil, Jung-gu, Seoul, 04620, Republic of Korea+82-2-2260-3114
Copyright(c) 2023 DONGGUK UNIVERSITY. ALL RIGHTS RESERVED.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.
