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蛛猴疱疹病毒Tio可在猴和人T细胞的生长转化中替代猴疱疹病毒StpC和Tip癌蛋白。

Herpesvirus ateles Tio can replace herpesvirus saimiri StpC and Tip oncoproteins in growth transformation of monkey and human T cells.

作者信息

Albrecht Jens-Christian, Biesinger Brigitte, Müller-Fleckenstein Ingrid, Lengenfelder Doris, Schmidt Monika, Fleckenstein Bernhard, Ensser Armin

机构信息

Institut für Klinische und Molekulare Virologie, Friedrich-Alexander-Universität Erlangen-Nürnberg, Schlossgarten 4, D-91054 Erlangen, Germany.

出版信息

J Virol. 2004 Sep;78(18):9814-9. doi: 10.1128/JVI.78.18.9814-9819.2004.

Abstract

Herpesvirus saimiri group C strains are capable of transforming human and simian T-lymphocyte populations to permanent antigen-independent growth. Two viral oncoproteins, StpC and Tip, that are encoded by a single bicistronic mRNA, act in concert to mediate this phenotype. A closely related New World monkey herpesvirus, herpesvirus ateles, transcribes a single spliced mRNA at an equivalent genome locus. The encoded protein, Tio, has sequence homologies to both StpC and Tip. We inserted the tio sequence of herpesvirus ateles strain 73 into a recombinant herpesvirus saimiri C488 lacking its own stpC/tip oncogene. Simian as well as human T lymphocytes were growth transformed by the chimeric Tio-expressing viruses. Thus, a single herpesvirus protein appears to be responsible for the oncogenic effects of herpesvirus ateles.

摘要

赛米利疱疹病毒C组毒株能够将人类和猿猴T淋巴细胞群体转化为永久性的不依赖抗原的生长状态。由单个双顺反子mRNA编码的两种病毒癌蛋白StpC和Tip协同作用介导这种表型。一种密切相关的新大陆猴疱疹病毒——蛛猴疱疹病毒,在等效的基因组位点转录出一条单一的剪接mRNA。所编码的蛋白Tio与StpC和Tip都具有序列同源性。我们将蛛猴疱疹病毒73株的tio序列插入到缺失自身stpC/tip癌基因的重组赛米利疱疹病毒C488中。表达嵌合Tio的病毒使猿猴以及人类T淋巴细胞发生生长转化。因此,单一的疱疹病毒蛋白似乎是蛛猴疱疹病毒致癌作用的原因。

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