Division of Virology, Aichi Cancer Center Research Institute, Kanokoden, Nagoya, Japan.
PLoS One. 2010 Jul 30;5(7):e11901. doi: 10.1371/journal.pone.0011901.
Human cytomegalovirus (HCMV) can be reactivated under immunosuppressive conditions causing several fatal pneumonitis, hepatitis, retinitis, and gastrointestinal diseases. HCMV also causes deafness and mental retardation in neonates when primary infection has occurred during pregnancy. In the genome of HCMV at least 194 known open reading frames (ORFs) have been predicted, and approximately one-quarter, or 41 ORFs, are required for viral replication in cell culture. In contrast, the majority of the predicted ORFs are nonessential for viral replication in cell culture. However, it is also possible that these ORFs are required for the efficient viral replication in the host. The UL77 gene of HCMV is essential for viral replication and has a role in viral DNA packaging. The function of the upstream UL76 gene in the HCMV-infected cells is not understood. UL76 and UL77 are cistons on the same viral mRNA and a conventional 5' mRNA for UL77 has not been detected. The vast majority of eukaryotic mRNAs are monocistronic, i.e., they encode only a single protein.
METHODOLOGY/PRINCIPAL FINDINGS: To determine whether the UL76 ORF affects UL77 gene expression, we mutated UL76 by ORF frame-shifts, stop codons or deletion of the viral gene. The effect on UL77 protein expression was determined by either transfection of expression plasmids or infection with recombinant viruses. Mutation of UL76 ORF significantly increased the level of UL77 protein expression. However, deletion of UL76 upstream of the UL77 ORF had only marginal effects on viral growth.
CONCLUSIONS/SIGNIFICANCE: While UL76 is not essential for viral replication, the UL76 ORF is involved in regulation of the level of UL77 protein expression in a manner dependent on the translation re-initiation. UL76 may fine-tune the UL77 expression for the efficient viral replication in the HCMV- infected cells.
人巨细胞病毒(HCMV)可在免疫抑制条件下重新激活,导致多种致命性肺炎、肝炎、视网膜炎和胃肠道疾病。HCMV 也会导致新生儿耳聋和智力迟钝,如果在怀孕期间发生原发性感染。在 HCMV 的基因组中,已经预测了至少 194 个已知的开放阅读框(ORF),大约四分之一,即 41 个 ORF,是在细胞培养中复制病毒所必需的。相比之下,大多数预测的 ORF 对于细胞培养中的病毒复制不是必需的。然而,这些 ORF 也可能是病毒在宿主中高效复制所必需的。HCMV 的 UL77 基因对病毒复制是必需的,并且在病毒 DNA 包装中起作用。在 HCMV 感染细胞中,UL76 基因的上游功能尚不清楚。UL76 和 UL77 是同一病毒 mRNA 上的顺式基因,尚未检测到 UL77 的常规 5' mRNA。绝大多数真核 mRNA 是单顺反子的,即它们只编码一种蛋白质。
方法/主要发现:为了确定 UL76 ORF 是否影响 UL77 基因表达,我们通过 ORF 移码、终止密码子或病毒基因缺失突变 UL76。通过转染表达质粒或感染重组病毒来确定 UL77 蛋白表达的影响。UL76 ORF 的突变显著增加了 UL77 蛋白表达的水平。然而,在 UL77 ORF 上游缺失 UL76 对病毒生长的影响只有轻微的影响。
结论/意义:虽然 UL76 不是病毒复制所必需的,但 UL76 ORF 参与了 UL77 蛋白表达水平的调节,这种调节方式依赖于翻译重新起始。UL76 可能微调 UL77 的表达,以实现 HCMV 感染细胞中病毒的高效复制。