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一种由选择性剪接的BK病毒早期mRNA表达的截短T抗原。

A truncated T antigen expressed from an alternatively spliced BK virus early mRNA.

作者信息

Abend Johanna R, Joseph Amy E, Das Dweepanita, Campbell-Cecen Deniz B, Imperiale Michael J

机构信息

Department of Microbiology and Immunology and Comprehensive Cancer Center, University of Michigan Medical School, Ann Arbor, MI 48109-5942, USA.

出版信息

J Gen Virol. 2009 May;90(Pt 5):1238-1245. doi: 10.1099/vir.0.009159-0. Epub 2009 Mar 4.

Abstract

The early region of BK virus (BKV) is known to encode two well-characterized tumour (T) antigens, large T antigen (TAg) and small T antigen (tAg). In this study, we provide evidence of a third early BKV mRNA that codes for an additional early region product with an apparent molecular mass of 17-20 kDa. This truncated form of TAg (truncTAg) is expressed from an alternatively spliced mRNA that is derived from the excision of a second intron from the mRNA encoding TAg. The first 133 aa of truncTAg are identical to those of TAg but the additional splice results in translation from a different reading frame, adding three new amino acids before reaching a stop codon. TruncTAg is expressed in both BKV-transformed and lytically infected cells and it is found to be primarily localized to the nucleus. The function of BKV truncTAg is likely to be relevant to transformation, similar to the additional T antigens of simian virus 40, JC virus and mouse polyomavirus.

摘要

已知BK病毒(BKV)的早期区域编码两种特征明确的肿瘤(T)抗原,即大T抗原(TAg)和小T抗原(tAg)。在本研究中,我们提供了第三条早期BKV mRNA的证据,该mRNA编码一种额外的早期区域产物,其表观分子量为17 - 20 kDa。这种截短形式的TAg(truncTAg)由一种可变剪接的mRNA表达,该mRNA源自从编码TAg的mRNA中切除第二个内含子。truncTAg的前133个氨基酸与TAg的相同,但额外的剪接导致从不同的阅读框进行翻译,在到达终止密码子之前添加了三个新的氨基酸。TruncTAg在BKV转化细胞和裂解感染细胞中均有表达,并且发现它主要定位于细胞核。BKV truncTAg的功能可能与转化有关,类似于猿猴病毒40、JC病毒和小鼠多瘤病毒的其他T抗原。

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