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dc.contributor.authorDalay, Nejat
dc.contributor.authorOzgur, Emre
dc.contributor.authorGezer, Ugur
dc.contributor.authorCetinkaya, Merve
dc.date.accessioned2021-03-03T16:55:23Z
dc.date.available2021-03-03T16:55:23Z
dc.date.issued2015
dc.identifier.citationCetinkaya M., Ozgur E., Dalay N., Gezer U., "Global quantification of heterochromatin-associated histone methylations in cell lines with differential sensitivity to ionizing radiation", ACTA BIOCHIMICA POLONICA, cilt.62, sa.2, ss.173-176, 2015
dc.identifier.issn0001-527X
dc.identifier.otherav_46f5ee5d-23b4-4fd9-a150-c2d8c1a868fa
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/51272
dc.identifier.urihttps://doi.org/10.18388/abp.2014_790
dc.description.abstractHistone modifications are involved in the DNA damage response (DDR). Here, by utilizing an ELISA immunoassay we assessed the methylation at H3K9 (H3K9me2 and H3K9me3) in two cell lines with differential sensitivity to radiation-induced apoptosis, He La (sensitive) and MCF-7 (resistant). We found that DNA damage induction by gamma-irradiation leads to considerable accumulation (up to 5-fold) of H3K9me2 and H3K9me3, but not of H4K20me3 (control modification) in MCF-7 cells (p<0.05). Interestingly, a lower dose (2 Gy) was more effective than 5 Gy. In He La cells a smaller effect (approx. 1.5-1.8-fold) was evident only at 5 Gy. In conclusion, our findings reveal that DNA damage leads to specific accumulation of H3K9me2 and H3K9me3 in a cell-type specific manner.
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectSitogenetik
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.titleGlobal quantification of heterochromatin-associated histone methylations in cell lines with differential sensitivity to ionizing radiation
dc.typeMakale
dc.relation.journalACTA BIOCHIMICA POLONICA
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume62
dc.identifier.issue2
dc.identifier.startpage173
dc.identifier.endpage176
dc.contributor.firstauthorID63836


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