View : 900 Download: 0

Full metadata record

DC Field Value Language
dc.contributor.author윤영대*
dc.contributor.author권종범*
dc.date.accessioned2018-05-18T08:15:05Z-
dc.date.available2018-05-18T08:15:05Z-
dc.date.issued2005*
dc.identifier.issn0264-6021*
dc.identifier.otherOAK-2748*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/243131-
dc.description.abstractDouble-strand breaks (DSBs) of chromosomal DNA trigger the cellular response that activates the pathways for DNA repair and cell-cycle checkpoints, and sometimes the pathways leading to cell death if the damage is too severe to be tolerated. Evidence indicates that, upon generation of DNA DSBs, many nuclear proteins that are involved in DNA repair and checkpoints are recruited to chromatin around the DNA lesions. In the present study we used a proteomics approach to identify DNA-damage-induced chromatin-binding proteins in a systematic way. Two-dimensional gel analysis for protein extracts of chromatin from DNA-damage-induced and control HeLa cells identified four proteins as the candidates for DNA-damage-induced chromatin-binding proteins. MALDI-TOF (matrix-assisted laser-desorption ionization-time-of-flight) MS analysis identified these proteins to be NPM (nucleophosmin), hnRNP (heterogeneous nuclear ribonucleoprotein) Cl, hnRNP C2 and 37-kDa laminin-receptor pre-cursor, and the identity of these proteins was further confirmed by immunoblot analysis with specific antibodies. We then demonstrated with chromatin-binding assays that NPM and hnRNP C1/C2, the abundant nuclear proteins with pleiotropic functions, indeed bind to chromatin in a DNA-damage-dependent manner, implicating these proteins in DNA repair and/or damage response. Immunofluorescence experiments showed that NPM, normally present in the nucleoli, is mobilized into the nucleoplasm after DNA damage, and that neither NPM nor hnRNP C1/C2 is actively recruited to the sites of DNA breaks. These results suggest that NPM and hnRNP C1/C2 may function at the levels of the global context of chromatin, rather than by specifically targeting the broken DNA. © 2005 Biochemical Society.*
dc.languageEnglish*
dc.titleA proteomics approach for the identification of nucleophosmin and heterogeneous nuclear ribonucleoprotein C1/C2 as chromatin-binding proteins in response to DNA double-strand breaks*
dc.typeArticle*
dc.relation.issue1*
dc.relation.volume388*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage7*
dc.relation.lastpage15*
dc.relation.journaltitleBiochemical Journal*
dc.identifier.doi10.1042/BJ20042033*
dc.identifier.wosidWOS:000229464800002*
dc.identifier.scopusid2-s2.0-19544375560*
dc.author.googleLee S.Y.*
dc.author.googlePark J.-H.*
dc.author.googleKim S.*
dc.author.googlePark E.-J.*
dc.author.googleYun Y.*
dc.author.googleKwon J.*
dc.contributor.scopusid윤영대(7201731033)*
dc.contributor.scopusid권종범(7202469069)*
dc.date.modifydate20240422113429*
Appears in Collections:
자연과학대학 > 생명과학전공 > Journal papers
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML


qrcode

BROWSE