Spector D J, Tevethia M J
Virology. 1986 Jun;151(2):329-38. doi: 10.1016/0042-6822(86)90053-x.
Human cytomegalovirus (HCMV) complements adenovirus mutant dl312, which is completely defective for expression of the adenovirus immediate early E1a gene region, for lytic growth (Tevethia and Spector, 1984). This assay defines at least one HCMV function, activation of the transcription of adenovirus early genes in trans, that must be provided for dl312 replication in coinfected cells. We show here that trans-activation depended on the expression of one or more HCMV gene. Human embryonic lung cells were transfected with dl312 DNA-protein complex and either HCMV DNA or recombinant plasmids containing the adenovirus E1a gene region or HCMV (Towne strain) DNA fragments. Replication of dl312 occurred only in cells that received both DPC and either the E1a gene, HCMV DNA, or the XbaI-E HCMV DNA fragment (0.68 to 0.77 map units). In addition, we show that HCMV also complemented adenovirus mutant pm975 for growth in 0.2% serum. Since pm975 grows poorly in low concentrations of serum due to a defect in an E1a gene product, this assay identified a second HCMV E1a-like function.
人巨细胞病毒(HCMV)可互补腺病毒突变体dl312进行裂解生长,dl312在腺病毒立即早期E1a基因区域的表达完全缺陷(特韦西亚和斯佩克特,1984年)。该检测方法定义了至少一种HCMV功能,即反式激活腺病毒早期基因的转录,这是共感染细胞中dl312复制所必需的。我们在此表明,反式激活依赖于一种或多种HCMV基因的表达。用人胚肺细胞转染dl312 DNA-蛋白质复合物以及HCMV DNA或含有腺病毒E1a基因区域的重组质粒或HCMV(汤氏株)DNA片段。dl312仅在同时接受DPC和E1a基因、HCMV DNA或XbaI-E HCMV DNA片段(0.68至0.77个图距单位)的细胞中发生复制。此外,我们还表明,HCMV在0.2%血清中生长时也能互补腺病毒突变体pm975。由于pm975在低浓度血清中生长不良是由于E1a基因产物存在缺陷,该检测方法确定了第二种HCMV E1a样功能。