Lai Fatt R B, Mak S
J Virol. 1982 Jun;42(3):969-77. doi: 10.1128/JVI.42.3.969-977.1982.
A function involved in the inhibition of DNA degradation has been assigned through complementation tests to a product of region E1b of the adenovirus genome (between 4.5 and 10.5 map units). DNA degradation induced by the adenovirus type 12 (Ad12) cyt mutant H12cyt70 and the Ad5 early deletion mutant dl313 (with the deletion between 3.5 and 10.7 map units) was inhibited by coinfection with Ad5 region E1a (between 0 and 4.5 map units) mutants dl312 and hr1 and region E1b mutant hr6. The defect of inhibition of DNA degradation in Ad5 dl313 was also complemented in 293 cells. This DNase-inhibitory function does not appear to involve polypeptide IX or the 58,000-dalton polypeptide. Wild-type Ad12 induced DNA degradation in hamster embryo cells, suggesting that the DNase-inhibitory function is not expressed in these nonpermissive cells. Additional evidence suggests the involvement of a second viral product which positively influences the DNase activity and which appears to be an early function.
通过互补试验已将一种参与抑制DNA降解的功能定位到腺病毒基因组E1b区(在4.5至10.5个图距单位之间)的一个产物上。12型腺病毒(Ad12)细胞突变体H12cyt70和Ad5早期缺失突变体dl313(缺失位于3.5至10.7个图距单位之间)诱导的DNA降解,可被与Ad5 E1a区(在0至4.5个图距单位之间)突变体dl312和hr1以及E1b区突变体hr6共感染所抑制。Ad5 dl313中抑制DNA降解的缺陷在293细胞中也得到了互补。这种DNA酶抑制功能似乎不涉及多肽IX或58,000道尔顿的多肽。野生型Ad12在仓鼠胚胎细胞中诱导DNA降解,这表明在这些非允许细胞中不表达DNA酶抑制功能。其他证据表明存在第二种病毒产物,它对DNA酶活性有正向影响,并且似乎是一种早期功能。