Hamid R, Cogan J D, Jones S N, Tibbetts C
Vanderbilt University School of Medicine, Nashville, Tennessee 37232-2363, USA.
Virology. 1995 Nov 10;213(2):666-70. doi: 10.1006/viro.1995.0039.
Different serotypes and evolutionary variants of human adenoviruses exhibit distinctive patterns of positive and negative autoregulation of the viral E1A gene. An autoregulatory E1A promoter mutation of the adenovirus type 3 (Ad3) E1A gene renders Ad3hr15 incapable of growth in normally permissive cells. The promoter mutation is complemented in trans by E1A products of the heterologous helper adenovirus type 5 (Ad5). Second-site revertants of Ad3hr15 restore viability with high levels of E1A gene expression. The revertant E1A genotypes retain the mutant E1A promoter and have small in-frame deletions in the nonconserved region between the repression- and activation-associated conserved domains CR2 and CR3. Plasmid expression vectors were constructed as 12S and 13S cDNA forms of revertant E1A genes. These were used in cotransfection experiments with a reporter gene plasmid under transcriptional control of the mutant Ad3hr15 E1A promoter. The repression of the Ad3hr15 E1A promoter by helper Ad5 or revertant 12S E1A cDNA was consistently greater than that effected wild-type Ad3 12S cDNAs expression. Significantly greater levels of positive transactivation were observed in cotransfections with 13S cDNAs of Ad5 or with the 13S E1A cDNA of Ad3hr15 revertants, compared to the transactivation observed with the mutant-encoded wild-type Ad3 13S E1A cDNA. The Ad5 helper and dI-revertant phenotype of Ad3hr15 appear to be related to transactivation activities of coexpressed E1A genes. The nonconserved region which separates the conserved coding regions CR2 and CR3 of the type 3 E1A gene acts to attenuate E1A-mediated repression and transactivation of transcription.
人类腺病毒的不同血清型和进化变体表现出病毒E1A基因独特的正负自调控模式。腺病毒3型(Ad3)E1A基因的自调控E1A启动子突变使Ad3hr15在正常允许细胞中无法生长。该启动子突变可被异源辅助腺病毒5型(Ad5)的E1A产物反式互补。Ad3hr15的第二位点回复突变体通过高水平的E1A基因表达恢复了活力。回复突变体E1A基因型保留了突变的E1A启动子,并且在抑制和激活相关保守结构域CR2和CR3之间的非保守区域有小的框内缺失。构建了回复突变体E1A基因的12S和13S cDNA形式的质粒表达载体。将这些载体用于与在突变型Ad3hr15 E1A启动子转录控制下的报告基因质粒的共转染实验。辅助Ad5或回复突变体12S E1A cDNA对Ad3hr15 E1A启动子的抑制作用始终大于野生型Ad3 12S cDNA表达所产生的抑制作用。与突变体编码的野生型Ad3 13S E1A cDNA所观察到的反式激活相比,在与Ad5的13S cDNA或Ad3hr15回复突变体的13S E1A cDNA共转染时观察到显著更高水平的正性反式激活。Ad3hr15的Ad5辅助和缺失-回复突变体表型似乎与共表达的E1A基因的反式激活活性有关。分隔3型E1A基因保守编码区CR2和CR3的非保守区域起到减弱E1A介导的转录抑制和反式激活的作用。