The Novel Oncogene Jcf1 in Development and Oncogenesis
The Novel Oncogene Jcf1 in Development and Oncogenesis
批准号:
7091330
负责人:
PHILIP N. TSICHLIS
金额:
$32.63万
依托单位:
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:
2004-07-01 至 2008-04-30
关键词:
3T3 cellsDrosophilidaeRNA interferencecarcinogenesisdevelopmental geneticsfluorescence microscopyfluorescent in situ hybridizationgene expressiongenetic regulationgenetic transcriptiongreen fluorescent proteinshuman tissuein situ hybridizationlaboratory mousemolecular cloningneoplasm /cancer geneticsnorthern blottingsoncogenesphenotypepolymerase chain reactionprotein protein interactionprotein structure functiontissue /cell culture
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): A genome-wide screen for loci of common integration in MoMuLV-induced rat T cell lymphomas, led to the identification of a novel oncogene, Jcf1, which is the subject of this proposal. Jcf1is unique among oncogenes, in that it promotes the growth of primary tumor cells in animals but is dispensable in culture. The protein encoded by this gene is 1336 amino acids long, contains a jumonji (JmjC) domain, a CXXC/PHD2 zinc finger domain, an F box and a leucine rich repeat (LRR) and is localized in the nucleus. Underscoring the importance of the JmjC domain, which is thought to be involved in chromatin modification and remodeling, was the finding that three additional provirus integrations among 146 cloned had targeted genes that also encode JmjC domain-containing proteins. A two-hybrid screen using the F-box/LRR domain as the bait identified several interacting proteins that are involved in transcription, DNA repair and the regulation of apoptosis. Moreover, stable or transient transfections of Jcf1in cell lines that express this gene at very low levels induced the expression of the endogenous gene, thus confirming that Jcf1is a regulator gene expression. Serum starvation of NIH 3T3 cells and IL-2 starvation of an IL-2 dependent T cell lymphoma line led to a precipitous drop in Jcf1expression. Reexposure to serum or IL-2 respectively induced Jcf1rapidly, suggesting that Jcf1may have a role in the reentry and progression of cells through the G1 phase of the cell cycle. Moreover, the expression of Jcf1declined to undetectable levels in the course of differentiation of a myelomonocytic cell line in culture suggesting that it may have a role in myeloid cell differentiation. Jcf1is a highly conserved protein. Using preexisting Jcf1Drosphila mutants, generated by P element insertions in the first two introns of the gene, we demonstrated that DJcf1 is required during development. Experiments proposed here will utilize molecular biology, tissue culture and genetic strategies to address the role of Jcf1in development and oncogenesis.
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资助金额:$28.97万
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海外基金