首页> 美国卫生研究院文献>Journal of Virology >Note: Human T-Cell Leukemia Virus Type 1 pX-I and pX-II Open Reading Frames Are Dispensable for the Immortalization of Primary Lymphocytes
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Note: Human T-Cell Leukemia Virus Type 1 pX-I and pX-II Open Reading Frames Are Dispensable for the Immortalization of Primary Lymphocytes

机译:注意:人类T细胞白血病病毒1型pX-I和pX-II开放阅读框对于永生化原代淋巴细胞是必不可少的

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摘要

Human T-cell leukemia virus type 1 (HTLV-1) infects and transforms CD4+ T-lymphocytes both in vivo and in vitro. Although the Tax protein of HTLV-1 has been strongly implicated as a transforming agent, other virally encoded proteins may also play a role in the transformation process. In addition to the rex and tax genes, the pX region of the HTLV-1 genome contains two open reading frames (pX-I and pX-II) which encode the putative viral accessory proteins known as p12I, p30II, and p13II. Mutations in the ACH molecular clone of HTLV-1 that are predicted to abrogate the expression of p12I, p13II and p30II were constructed. These mutations had no effect on viral replication or the immortalization of primary lymphocytes. Although these proteins are dispensable for viral replication and immortalization in vitro, it remains possible that they alter infection in vivo.
机译:1型人T细胞白血病病毒(HTLV-1)在体内和体外均可感染并转化CD4 + T淋巴细胞。尽管已经强烈暗示了HTLV-1的Tax蛋白是转化剂,但其他病毒编码的蛋白也可能在转化过程中起作用。除了rex和tax基因外,HTLV-1基因组的pX区还包含两个开放阅读框(pX-I和pX-II),它们编码假定的病毒辅助蛋白,称为p12 I ,p30 II 和p13 II 。在HTLV-1 ACH分子克隆中构建了有望消除p12 I ,p13 II 和p30 II 表达的突变。这些突变对病毒复制或原代淋巴细胞永生化没有影响。尽管这些蛋白对于体外病毒复制和永生化是必不可少的,但它们仍可能在体内改变感染。

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