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Mitochondrial ribosomal protein L41 mediates serum starvation-induced cell-cycle arrest through an increase of p21WAF1/CIP1

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dc.contributor.author김형중-
dc.date.accessioned2017-05-04T07:38:19Z-
dc.date.available2017-05-04T07:38:19Z-
dc.date.issued2005-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/147571-
dc.description.abstractRibosomal proteins not only act as components of the translation apparatus but also regulate cell proliferation and apoptosis. A previous study reported that MRPL41 plays an important role in p53-dependent apoptosis. It also showed that MRPL41 arrests the cell cycle by stabilizing p27Kip1 in the absence of p53. This study found that MRPL41 mediates the p21WAF1/CIP1-mediated G1 arrest in response to serum starvation. The cells were released from serum starvation-induced G1 arrest via the siRNA-mediated blocking of MRPL41 expression. Overall, these results suggest that MRPL41 arrests the cell cycle by increasing the p21WAF1/CIP1 and p27Kip1 levels under the growth inhibitory conditions.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherElsevier-
dc.relation.isPartOfBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdenocarcinoma/metabolism*-
dc.subject.MESHCarrier Proteins/metabolism*-
dc.subject.MESHCell Cycle Proteins/metabolism*-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHCulture Media, Serum-Free-
dc.subject.MESHCyclin-Dependent Kinase Inhibitor p21/metabolism*-
dc.subject.MESHG1 Phase*-
dc.subject.MESHHumans-
dc.subject.MESHLung Neoplasms/metabolism*-
dc.subject.MESHMitochondrial Proteins-
dc.subject.MESHRibosomal Proteins/metabolism*-
dc.subject.MESHSerum/metabolism-
dc.titleMitochondrial ribosomal protein L41 mediates serum starvation-induced cell-cycle arrest through an increase of p21WAF1/CIP1-
dc.typeArticle-
dc.publisher.locationUnited States-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorMi Jin Kim-
dc.contributor.googleauthorYoung A. Yoo-
dc.contributor.googleauthorHyung Jung Kim-
dc.contributor.googleauthorSeongman Kang-
dc.contributor.googleauthorYong Geon Kim-
dc.contributor.googleauthorJun Suk Kim-
dc.contributor.googleauthorYoung Do Yoo-
dc.identifier.doi10.1016/j.bbrc.2005.10.064-
dc.contributor.localIdA01158-
dc.relation.journalcodeJ00281-
dc.identifier.eissn1090-2104-
dc.identifier.pmid16256947-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0006291X05023193-
dc.subject.keywordMRPL41-
dc.subject.keywordp21WAF1/CIP1-
dc.subject.keywordSerum starvation-
dc.subject.keywordp53-
dc.subject.keywordCell cycle-
dc.subject.keywordp27Kip1-
dc.contributor.alternativeNameKim, Hyung Jung-
dc.citation.volume338-
dc.citation.number2-
dc.citation.startPage1179-
dc.citation.endPage1184-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, Vol.338(2) : 1179-1184, 2005-
dc.date.modified2017-05-04-
dc.identifier.rimsid40344-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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