Koralnik I J, Gessain A, Klotman M E, Lo Monico A, Berneman Z N, Franchini G
Laboratory of Tumor Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1992 Sep 15;89(18):8813-7. doi: 10.1073/pnas.89.18.8813.
The pX region of the human T-cell leukemia/lymphotropic virus type I (HTLV-I) contains at least four open reading frames (orfI-orfIV). orf III and orf IV encode the regulatory HTLV-I proteins Rex and Tax, which together modulate viral expression, and the p21rex protein of unknown function. By using the reverse transcriptase and polymerase chain reaction techniques on the RNA of an HTLV-I-infected cell culture, we uncovered the existence of alternatively spliced mRNAs generated through the use of three splice acceptor sites. These mRNAs encoded protein isoforms derived from the HTLV-I orf I (p12I) and orf II (p13II and p30II). An additional acceptor splice site, used in the processing of the env and tax/rex mRNAs and a singly spliced mRNA for the p21rex protein, was also identified. All of these HTLV-I mRNAs were also detected in freshly isolated cells from HTLV-I-infected individuals. Thus HTLV-I, like the human immunodeficiency virus type 1, has developed fine posttranscriptional mechanisms to increase the complexity of its genome.
人类I型嗜T细胞白血病/淋巴瘤病毒(HTLV-I)的pX区域至少包含四个开放阅读框(orfI - orfIV)。orf III和orf IV编码调节性HTLV-I蛋白Rex和Tax,它们共同调节病毒表达,以及功能未知的p21rex蛋白。通过对HTLV-I感染的细胞培养物的RNA使用逆转录酶和聚合酶链反应技术,我们发现了通过使用三个剪接受体位点产生的可变剪接mRNA的存在。这些mRNA编码源自HTLV-I orf I(p12I)和orf II(p13II和p30II)的蛋白质异构体。还鉴定了一个额外的剪接受体位点,其用于env和tax/rex mRNA的加工以及p21rex蛋白的单剪接mRNA。所有这些HTLV-I mRNA也在来自HTLV-I感染个体的新鲜分离细胞中被检测到。因此,HTLV-I与人类免疫缺陷病毒1型一样,已经发展出精细的转录后机制来增加其基因组的复杂性。