Mori Y, Yagi H, Shimamoto T, Isegawa Y, Sunagawa T, Inagi R, Kondo K, Tano Y, Yamanishi K
Departments of Microbiology, Ophthalmology, Osaka University Medical School, 2-2 Yamada-oka, Suita, Osaka, 565-0871, Japan.
Virology. 1998 Sep 15;249(1):129-39. doi: 10.1006/viro.1998.9305.
The US22 gene family was first discovered in human cytomegalovirus (HCMV) and contains several conserved amino acid motifs. Human herpesvirus 6 (HHV-6) also encodes several genes belonging to the US22 family, including the U3 gene (a positional homolog of HCMV UL24). Because the gene products of the US22 gene family function as gene regulators in general, we analyzed the HHV-6A U3 gene. Six transcripts with different molecular weights of 7.5-1.8 kb were detected by Northern blot analysis using a U3-specific probe. Sequence analyses of the respective cDNA clones and primer extension experiments revealed that the U3 gene encoded the 2.0- and 3.5-kb transcripts and had no splicing within the U3 gene region. By immunofluorescence testing using antibodies raised to a fusion protein of MBP (maltose-binding protein) and U3, the U3 viral antigen was detected as early as 24 h p.i. in HHV-6A-infected U373 cells. The antigens were found in cytoplasmic granules, preferentially in the endoplasmic reticulum. Moreover, cotransfection assay using a luciferase gene expression system revealed that the U3 gene product was capable of activating the human immunodeficiency virus long terminal repeat promoter in CV1 cells.
US22基因家族最初是在人巨细胞病毒(HCMV)中发现的,包含几个保守的氨基酸基序。人类疱疹病毒6型(HHV-6)也编码几个属于US22家族的基因,包括U3基因(HCMV UL24的位置同源物)。由于US22基因家族的基因产物通常作为基因调节因子发挥作用,我们分析了HHV-6A U3基因。使用U3特异性探针通过Northern印迹分析检测到六种分子量在7.5 - 1.8 kb之间的不同转录本。对各个cDNA克隆的序列分析和引物延伸实验表明,U3基因编码2.0 kb和3.5 kb的转录本,并且在U3基因区域内没有剪接。通过使用针对MBP(麦芽糖结合蛋白)和U3的融合蛋白产生的抗体进行免疫荧光测试,在HHV-6A感染的U373细胞中,早在感染后24小时就检测到了U3病毒抗原。这些抗原存在于细胞质颗粒中,优先在内质网中。此外,使用荧光素酶基因表达系统的共转染试验表明,U3基因产物能够在CV1细胞中激活人类免疫缺陷病毒长末端重复启动子。