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DNA Damage-Induced Foci of E2 Ubiquitin-Conjugating Enzyme are Detectable upon Co-transfection with an Interacting E3 Ubiquitin Ligase

机译:与相互作用的E3泛素连接酶共转染后,可检测到E2泛素结合酶的DNA损伤诱导灶。

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摘要

DNA damage repair elements accumulate at DNA damage sites to form ionizing radiation-induced foci (IRIF) for damage repair. IRIF, which represent direct evidence of DNA damage response activity, which are conveniently to be observed via immunofluorescence staining. Protein ubiquitination plays an important role in initiating the DNA damage response. Following DNA damage, the substrate binding protein E3 ubiquitin-ligases enzymes are recruited to DNA damage sites, then the E2 ubiquitin-conjugating enzymes are recruited to these sites by the E3 where they catalyze protein ubiquitination. However, IRIF of E2 enzymes are relatively transient and unstable in vivo and difficult to detect. Here, we present a new method for the observation of E2 IRIF. This method is based on the co-transfection of interacting E2 and E3 enzymes into cells and identifies IRIF via immunofluorescence following DNA damage.
机译:DNA损伤修复元件积聚在DNA损伤部位,形成电离辐射诱导病灶(IRIF)进行损伤修复。 IRIF代表DNA损伤反应活性的直接证据,可通过免疫荧光染色方便地观察到。蛋白质泛素化在引发DNA损伤反应中起重要作用。 DNA损伤后,底物结合蛋白E3泛素连接酶被募集到DNA损伤位点,然后E2泛素结合酶被E3募集到这些位点,在那里它们催化蛋白泛素化。然而,E2酶的IRIF在体内是相对短暂且不稳定的,并且难以检测。在这里,我们提出了一种观察E2 IRIF的新方法。该方法基于相互作用的E2和E3酶共转染到细胞中,并通过DNA损伤后的免疫荧光鉴定IRIF。

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