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来自原发性渗出性淋巴瘤的卡波西肉瘤相关疱疹病毒K12转录本含有复杂的重复元件,经过剪接,并从一个新的启动子起始转录。

The Kaposi's sarcoma-associated herpesvirus K12 transcript from a primary effusion lymphoma contains complex repeat elements, is spliced, and initiates from a novel promoter.

作者信息

Li Hong, Komatsu Takashi, Dezube Bruce J, Kaye Kenneth M

机构信息

Department of Medicine, Channing Laboratory, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02215, USA.

出版信息

J Virol. 2002 Dec;76(23):11880-8. doi: 10.1128/jvi.76.23.11880-11888.2002.

Abstract

Kaposi's sarcoma-associated herpesvirus (KSHV) latently infects KS tumors, primary effusion lymphomas (PELs), and PEL cell lines. K12 (T0.7) is the most abundant transcript expressed in latent KSHV infection. We characterize here the K12 transcript from a PEL tumor prior to passage in cell culture. The PEL tumor KSHV K12 transcript contained additional complex nucleotide repeat elements compared to the previously described K12 message of the BCBL-1 PEL cell line. The PEL tumor lacked kaposin B, the predominant BCBL-1 K12 protein product, but encoded kaposins A and C. The K12 transcript was spliced and the splicing event occurred in all KSHV isolates tested. The 5' end of the K12 transcript was mapped by 5' RACE (rapid amplification of cDNA ends) and S1 nuclease protection assays and was at the site of an active promoter. This work demonstrates that the K12 transcript contains variable, complex repeat elements, is spliced and is expressed from a novel KSHV promoter.

摘要

卡波西肉瘤相关疱疹病毒(KSHV)潜伏感染卡波西肉瘤肿瘤、原发性渗出性淋巴瘤(PEL)以及PEL细胞系。K12(T0.7)是潜伏性KSHV感染中表达量最高的转录本。我们在此对一株未经细胞培养传代的PEL肿瘤中的K12转录本进行了特征分析。与先前描述的BCBL - 1 PEL细胞系的K12信息相比,该PEL肿瘤的KSHV K12转录本包含额外的复杂核苷酸重复元件。该PEL肿瘤缺乏卡波辛B(BCBL - 1 K12的主要蛋白产物),但编码卡波辛A和C。K12转录本发生了剪接,且剪接事件在所有测试的KSHV分离株中均有发生。通过5' RACE(cDNA末端快速扩增)和S1核酸酶保护试验对K12转录本的5'端进行了定位,其位于一个活性启动子位点。这项工作表明,K12转录本包含可变的复杂重复元件,发生了剪接,并由一个新的KSHV启动子表达。

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