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A silence element involved in Kaposis sarcoma-associated herpesvirus ORF11 gene expression.

机译:沉默元件参与卡波氏肉瘤相关疱疹病毒ORF11基因表达。

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摘要

Kaposi's sarcoma-associated herpesvirus (KSHV also known as Human herpesvirus 8) is the etiological agent of Kaposi's sarcoma (KS) (1, 2, 12, 15), a disease of endothe-lial origin (14). KSHV infection has also been implicated in the etiology of two B-cell lymphoproliferative diseases, e.g. primary effusion lymphoma and multicentric Castle-mans disease (3,4,18). The KSHV ORF11 is a lytic viral gene with delayed-early expression kinetics (7). Little is known about ORF 11 protein function in KS or primary effusion lymphoma tumors. The discovery of a dUTPase like domain in ORF11 coding sequence suggests that ORF11 protein may function as a dUTPase (8). It is still controversial, whether ORF 11 functions like the dUTPase, since the functional dUTPase activity has not been formally demonstrated (16). The association of ORF 11 with tegument protein ORF45 suggests that ORF 11 may function in KSHV virion morphology, latency establishment, or host interaction (22).
机译:卡波西氏肉瘤相关疱疹病毒(KSHV也称为人疱疹病毒8)是卡波西氏肉瘤(KS)(1,2,12,15)的病原体,是一种内皮源性疾病(14)。 KSHV感染还与两种B细胞淋巴增生性疾病的病因有关,例如原发性积液性淋巴瘤和多中心Castle-Mans病(3、4、18)。 KSHV ORF11是一种裂解病毒基因,具有较早的表达动力学(7)。关于KS或原发性积液性淋巴瘤肿瘤中ORF 11蛋白功能的了解甚少。在ORF11编码序列中发现了类似dUTPase的结构域,这表明ORF11蛋白可能起着dUTPase的作用(8)。 ORF 11是否像dUTPase一样发挥作用仍是有争议的,因为尚未正式证明其功能性dUTPase活性(16)。 ORF 11与外皮蛋白ORF45的关联表明,ORF 11可能在KSHV病毒体形态,潜伏期建立或宿主相互作用中起作用(22)。

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