Dissection of a fundamental step in gene activation using the HTLV-1-encoded Tax

描述（由申请人提供）：人t细胞白血病病毒1型（HTLV-1）是一种与成人t细胞白血病（ATL）病原学相关的逆转录病毒。ATL是一种预后较差的恶性肿瘤。尽管估计有1500 - 2500万人感染HTLV，但这些感染中只有2- 5%发展为ATL（回顾见[2]）。在感染细胞的恶性转化中，主要参与者是病毒表达的癌蛋白Tax。税是

DESCRIPTION (provided by applicant): The human T-cell leukemia virus type-1 (HTLV-1) is a retrovirus etiologically associated with Adult T-cell Leukemia (ATL). ATL is a malignant cancer associated with poor prognosis. Although 15-25 million people are estimated to be infected with HTLV, only 2-5 percent of these infections develop into ATL (for review see [2]). A major player in the malignant transformation of infected cells is the virally expressed oncoprotein, Tax. Tax is a potent activator of transcription from the HTLV-1 promoter. Tax recruits the cellular proteins cAMP-response element binding protein (CREB) and p300/CREB-binding protein (CBP) to viral CRE sites located in the HTLV-1 LTR (for review see [1]). CBP/p300 is involved in numerous cellular pathways and understandably, deficiencies in CBP/p300 cause many types of cancer. Despite the participation of CBP/p300 in the regulation of many cellular pathways, little is known about the mechanism or its role in coactivator-mediated gene activation. We propose that a major activity of CBP/p300 is to recruit general transcriptional machinery to the promoter and that Tax stimulates this activity by binding to CBP/p300. This binding likely initiates structural changes in distinct domains of CBP/p300 that favor recruitment of general transcriptional machinery. Overall, the proposed studies will utilize interaction assays with targeted point mutants, individual domain isolations and deletions that target the interactions between Tax-CBP/p300. Competition and activity assays will enable us to functionally and biophysically characterize Tax-CBP/p300 interactions. Tax and CBP/p300 mutants developed will also be used to investigate structural changes in various domains of CBP/p300 and how these binding- induced changes relate to transcriptional machinery recruitment and activity. These studies have implications for viral and cellular mechanisms of activation, adding to the generally weak knowledge base on the role of coactivator contribution to this process.