Herpesviral Gene Expression in Kaposis Sarcoma

卡波济肉瘤中疱疹病毒基因的表达

• 批准号: 6407098
• 负责人: DON GANEM
• 金额: $ 27.55万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 1996
• 资助国家: 美国
• 起止时间: 1996-09-30 至 2006-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6407098
• 关键词: Kaposi's sarcoma; athymic mouse; cyclins; gene expression; gene targeting; genetic transcription; genetically modified animals; human herpesvirus 8; latent virus infection; lymphoma; neoplasm /cancer epidemiology; nuclear factor kappa beta; protein structure function; ribonucleoproteins; vascular endothelium; virus genetics; virus protein; virus replication

Infection by Kaposi's sarcoma-associated herpesvirus (KSHV; also called human herpesvirus 8) is a key factor in the development of Kaposi's sarcoma (KS), a proliferative lesion of endothelial cells that until recently was the commonest neoplasm of AIDS patients. In KS tumors, the viral genome resides within the majority of spindle cells in a latent state; smaller numbers of tumor cells display lytic infection. This grant began with the examination of viral gene expression in KS tumors, identifying several latent and lytic genes expressed in that context. The present renewal application seeks to further characterize the expression and function of these genes. Specifically, we will (i) develop an endothelial cell culture model of KSHV latency and use it to develop a genetic system for the creation and analysis of mutant KSHV genomes; (ii) characterize the phenotypic consequences of expression of a major KSHV latency locus encoding orfs 71,72 and 73; (iii) further explore the mechanisms and consequences of constitutive signaling by the KSHV K1 protein; (iv) characterize the biochemical activities and interactions of the KSHV kaposin gene products; and (v) identify the constituents of an abundant viral ribonucleoprotein complex and determine their function.

卡波西肉瘤相关疱疹病毒（KSHV，也称为人类疱疹病毒8）的感染是卡波西肉瘤（KS）发展的关键因素，卡波西肉瘤是一种内皮细胞的增生性病变，直到最近才成为艾滋病患者最常见的肿瘤。在KS肿瘤中，病毒基因组以潜伏状态驻留在大多数梭形细胞中；少量肿瘤细胞表现为溶解性感染。这项资助始于检查KS肿瘤中的病毒基因表达，确定了在这种情况下表达的几个潜伏和裂解基因。目前的更新申请旨在进一步表征这些基因的表达和功能。具体来说，我们将(i)开发内皮细胞培养KSHV潜伏期模型，并使用它来开发用于创建和分析突变KSHV基因组的遗传系统；（ii）描述编码orfs 71、72和73的主要KSHV潜伏期位点表达的表型后果；（iii）进一步探索KSHV K1蛋白构成信号传导的机制和后果；（iv）表征KSHV卡蛋白基因产物的生化活性和相互作用；(v)鉴定丰富的病毒核糖核蛋白复合物的成分并确定其功能。