E2-Cellular Complexes in HPV Chromatin Transcription
E2-Cellular Complexes in HPV Chromatin Transcription
批准号:
7234344
负责人:
CHENG-MING CHIANG
金额:
$5.77万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-08-01 至 2007-06-30
中文摘要
描述(由申请人提供):人乳头瘤病毒(HPV)可诱导多种人类疾病,包括生殖器疣和宫颈癌。HPV基因表达的调控主要由病毒编码的E2蛋白和细胞转录因子控制。 尽管已经使用裸病毒DNA基因组对HPV转录进行了许多研究,但对导致从HPV染色质开始转录的分子事件知之甚少,HPV染色质代表与细胞核心组蛋白复合的HPV基因组的浓缩形式。染色质的形成阻止细胞转录机制的进入,从而抑制HPV基因表达。为了鉴定促进HPV染色质转录的蛋白质因子,并进一步确定转录事件的分子机制,我们提出了以下两个目标。1)鉴定与HPV E2蛋白协同作用的细胞蛋白。天然组装的E2-细胞复合物已从人293衍生的细胞系中部分纯化,所述细胞系条件性表达不同形式的FLAG标记的HPV-11 E2蛋白。我们的发现是,人SWI/SNF染色质重塑复合物、GCN 5组蛋白乙酰转移酶和一般转录因子TFIID存在于2-MDa E2-细胞复合物中,并且具有推定辅阻遏物功能的一组不同的细胞蛋白与另一种E2-细胞复合物相关,这表明E2的N-末端结构域可能在功能上招募SWI/SNF,GCN 5和TFIID启动HPV染色质转录,并且E2还可以在转录过程中转换其相互作用伴侣以进一步调节HPV基因表达。这些假设将通过进行染色质重塑和组蛋白乙酰转移酶/脱乙酰酶测定,以及通过进行重建的无细胞转录和蛋白质-蛋白质和蛋白质-DNA相互作用研究来检验。2)探讨E2-细胞复合体在HPV染色质转录中的功能作用。 我们将通过使用单独纯化的染色质组装因子的重组HPV染色质转录测定以及使用条件性表达不同形式的HPV E2和E1蛋白的人HeLa衍生细胞系的体内染色质免疫沉淀研究来定义E2-细胞复合物的作用。总的来说,这些研究将揭示人SWI/SNF,GCN 5,TFIID和其他细胞因子在E2介导的HPV染色质转录中的作用,其模拟体内发现的天然存在的HPV基因组,并且还揭示了导致染色质转录的有效起始的分子事件。
英文摘要
DESCRIPTION (provided by applicant): Human papillomaviruses (HPVs) induce a variety of human diseases including genital warts and cervical carcinomas. Regulation of HPV gene expression is mainly controlled by virus-encoded E2 proteins and cellular transcription factors. Although many studies have been conducted on HPV transcription using naked viral DNA genomes, very little is known about the molecular events leading to initiation of transcription from HPV chromatin, which represents a condensed form of the HPV genome in complex with cellular core histone proteins. Formation of chromatin prevents access of the cellular transcription machinery and thereby inhibits HPV gene expression. To identify protein factors that facilitate transcription from HPV chromatin and to further define the molecular mechanism underlying transcriptional events, we propose the following two aims. 1) To identify cellular proteins working in conjunction with HPV E2 protein. Naturally assembled E2- cellular complexes have been partially purified from human 293-derived cell lines that conditionally express different forms of FLAG-tagged HPV-11 E2 proteins. Our findings that human SWI/SNF chromatin remodeling complex, GCN5 histone acetyltransferase and general transcription factor TFIID are found in a 2-MDa E2-cellular complex and a different set of cellular proteins with putative corepressor function is associated with another E2-cellular complex suggest that the N-terminal domain of E2 may functionally recruit SWI/SNF, GCN5 and TFIID to initiate HPV chromatin transcription and also E2 may switch its interacting partners during the transcriptional process to further modulate HPV gene expression. These hypotheses will be tested by performing chromatin remodeling and histone acetyltransferase/deacetylase assays, as well as by conducting reconstituted cell-free transcription and protein-protein and protein-DNA interaction studies. 2) To dissect the functional role of E2-cellular complexes in HPV chromatin transcription. We will define the role of E2-cellular complexes by reconstituted HPV chromatin transcription assays using individually purified chromatin assembly factors as well as by in vivo chromatin immunoprecipitation studies using human HeLa-derived cell lines conditionally expressing different forms of HPV E2 and E1 proteins. Collectively, these studies will uncover the role of human SWI/SNF, GCN5, TFIID and other cellular factors in E2-mediated transcription of HPV chromatin, which mimics naturally occurring HPV genomes found in vivo, and also shed light on the molecular events leading to a productive initiation of chromatin transcription.
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