Mohammadi Elham S, Ketner Elizabeth A, Johns David C, Ketner Gary
Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, 615 North Wolfe Street, Baltimore, MD 21205, USA.
Nucleic Acids Res. 2004 May 11;32(8):2652-9. doi: 10.1093/nar/gkh593. Print 2004.
The human adenovirus E4 ORF 6 34 kDa oncoprotein (E4 34k), in concert with the 55 kDa product of E1b, prevents concatenation of viral genomes in infected cells, inhibits the repair of double strand breaks (DSBs) in the viral genome, and inhibits V(D)J recombination in a plasmid transfection assay. These activities are consistent with a general inhibition by the E4 34k and E1b 55k proteins of DSB repair by non-homologous end joining (NHEJ) on extrachromosomal substrates. To determine whether inhibition of NHEJ extends to repair of DSBs in the cell chromosome, we have examined the effects of E4 34k on repair of chromosomal DSBs induced by ionizing radiation in a cell line in which E4 34k expression and biological activity is inducible and E1b 55k is produced constitutively. We demonstrate that in this cell line, induction of E4 34k inhibits chromosomal DSB repair. Recently, it has been shown that in infected cells, E4 34k and the adenovirus E1b 55k proteins cooperate to destabilize Mre11 and Rad50, components of mammalian NHEJ systems. Consistent with this, induction of expression of E4 34k in the inducible cell line also reduces the steady state level of Mre11 protein.
人腺病毒E4开放阅读框6的34 kDa癌蛋白(E4 34k)与E1b的55 kDa产物协同作用,可防止感染细胞中病毒基因组的串联,抑制病毒基因组中双链断裂(DSB)的修复,并在质粒转染试验中抑制V(D)J重组。这些活性与E4 34k和E1b 55k蛋白对染色体外底物上非同源末端连接(NHEJ)修复DSB的普遍抑制作用一致。为了确定NHEJ的抑制是否扩展到细胞染色体中DSB的修复,我们研究了E4 34k对电离辐射诱导的染色体DSB修复的影响,该细胞系中E4 34k的表达和生物活性是可诱导的,且E1b 55k是组成性产生的。我们证明,在该细胞系中,E4 34k的诱导抑制了染色体DSB的修复。最近,研究表明,在感染细胞中,E4 34k和腺病毒E1b 55k蛋白协同作用,使哺乳动物NHEJ系统的组成部分Mre11和Rad50不稳定。与此一致的是,在可诱导细胞系中E4 34k表达的诱导也降低了Mre11蛋白的稳态水平。