Tang Qiyi, Murphy Eain A, Maul Gerd G
The Wistar Institute, 3601 Spruce Street, Philadelphia, PA 19104, USA.
J Virol. 2006 Jul;80(14):6873-82. doi: 10.1128/JVI.00275-06.
Murine cytomegalovirus (MCMV) and human CMV (HCMV) share many features making the mouse system a potential small-animal model for HCMV. Although the genomic DNA sequence and the predicted open reading frames (ORFs) of MCMV have been determined, experimental evidence that the ORFs are actually transcribed has been lacking. We developed an MCMV global-DNA microarray that includes all previously predicted ORFs and 14 potential ones. A total of 172 ORFs were confirmed to be transcribed, including 7 newly discovered ORFs not previously predicted. No gene products from 10 previously predicted ORFs were detected by either DNA microarray analysis or reverse transcriptase PCR in MCMV-infected mouse fibroblasts, although 2 of those were expressed in a macrophage cell line, suggesting that potential gene products from these open reading frames are silenced in fibroblasts and required in macrophages. Immunohistochemical localization of the six newly described ORF products and three recently identified ones in cells transfected with the respective construct revealed four of the products in the nucleus and five in mitochondria. Analysis of two ORFs using site-directed mutagenesis showed that deletion of one of the mitochondrion-localized gene products led to significantly decreased replication in fibroblasts.
小鼠巨细胞病毒(MCMV)和人类巨细胞病毒(HCMV)具有许多共同特征,这使得小鼠系统成为HCMV潜在的小动物模型。尽管已经确定了MCMV的基因组DNA序列和预测的开放阅读框(ORF),但一直缺乏ORF实际转录的实验证据。我们开发了一种MCMV全基因组DNA微阵列,其中包括所有先前预测的ORF和14个潜在的ORF。总共172个ORF被证实可以转录,包括7个先前未预测到的新发现的ORF。在MCMV感染的小鼠成纤维细胞中,通过DNA微阵列分析或逆转录酶PCR均未检测到10个先前预测的ORF的基因产物,尽管其中2个在巨噬细胞系中表达,这表明这些开放阅读框的潜在基因产物在成纤维细胞中沉默,而在巨噬细胞中是必需的。在用相应构建体转染的细胞中,对六个新描述的ORF产物和三个最近鉴定的ORF产物进行免疫组织化学定位,结果显示其中四个产物位于细胞核中,五个位于线粒体中。使用定点诱变对两个ORF进行分析表明,线粒体定位的基因产物之一的缺失导致成纤维细胞中的复制显著减少。