Department of Pathology, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku, Tokyo 162-8640, Japan.
Virology. 2010 Mar 15;398(2):273-9. doi: 10.1016/j.virol.2009.12.024. Epub 2010 Jan 13.
To clarify whether mutations in the large T gene encoded by Merkel cell polyomavirus affect the expression and function of large T antigen in Merkel cell carcinoma cases, we investigated the expression of large T antigen in vitro and in vivo. Immunohistochemistry using a rabbit polyclonal antibody revealed that large T antigen was expressed in the nuclei of Merkel cell carcinoma cells with Merkel cell polyomavirus infection. Deletion mutant analyses identified an Arg-Lys-Arg-Lys sequence (amino acids 277-280) as a nuclear localization signal in large T antigen. Sequence analyses revealed that there were no mutations in the nuclear localization signal in any of the eleven Merkel cell polyomavirus strains examined. Furthermore, stop codons were not observed in the upstream of the nuclear localization signal in any of the Merkel cell carcinoma cases examined. These data suggest that the nuclear localization signal is highly conserved and functional in Merkel cell carcinoma cases.
为了阐明 Merkel 细胞多瘤病毒(Merkel cell polyomavirus)大 T 基因编码的突变是否影响 Merkel 细胞癌(Merkel cell carcinoma)病例中大 T 抗原的表达和功能,我们研究了大 T 抗原在体外和体内的表达。使用兔多克隆抗体的免疫组织化学显示,Merkel 细胞多瘤病毒感染的 Merkel 细胞癌细胞的核内表达大 T 抗原。缺失突变分析确定 Arg-Lys-Arg-Lys 序列(氨基酸 277-280)是大 T 抗原中的核定位信号。序列分析显示,在所研究的 11 株 Merkel 细胞多瘤病毒株中,核定位信号均无突变。此外,在所研究的 Merkel 细胞癌病例中,核定位信号上游均未观察到终止密码子。这些数据表明,核定位信号在 Merkel 细胞癌病例中高度保守且具有功能。