Post-translational Modifications of High-mobility Group Proteins
Post-translational Modifications of High-mobility Group Proteins
批准号:
7209245
负责人:
Yinsheng Wang
金额:
$22.8万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-08-01 至 2010-07-31
关键词:
AcetylationAdoptedAffectAmino AcidsApoptosisBindingBiologicalBiological MarkersCancer PrognosisCancer cell lineCell LineCellsDevelopmentDiagnosisElementsEstrogen ReceptorsEstrogensGeneral Transcription FactorsGenetic TranscriptionGoalsHMGN1 ProteinHMGN1 geneHMGN2 geneHigh Mobility Group ProteinsHistonesHumanIn VitroIndividualIonsLaboratoriesMalignant - descriptorMalignant NeoplasmsMammary Gland ParenchymaMass Spectrum AnalysisMetabolicMethylationMitogen-Activated Protein KinasesMolecularNatureNeoplasm MetastasisNon-Histone Chromosomal ProteinsNumbersOutcomePhosphorylationPhosphorylation SitePhosphotransferasesPost-Translational Protein ProcessingPrincipal InvestigatorProtein KinaseProteinsRoleSiteSolidSourceStable Isotope LabelingStaphylococcal Protein ATestingTimeTissuesTranscriptional Regulationbasecancer cellcancer diagnosiscasein kinase IIglycosylationin vivoinsightmass spectrometerneoplastic celloutcome forecastprogramsresearch studytandem mass spectrometrytumor progression
中文摘要
描述(由申请人提供):该项目的长期目标是了解非组蛋白染色体高迁移率组(HMG)蛋白翻译后修饰的生物学意义。HMG蛋白是公认的通用转录因子,它们可以通过磷酸化、甲基化、乙酰化和糖基化等多种翻译后修饰。我们的假设是,HMG蛋白不仅表达,而且翻译后修饰与癌症进展和恶性转化有关。为了验证这一假设,我们根据以下具体目的提出了实验:目的1,系统地检查正常细胞和癌细胞中HMG蛋白的翻译后修饰;目的2,研究HMG蛋白的表达水平和翻译后修饰的性质是否与癌症进展相关;目的3:在体外研究纯化蛋白激酶对HMG蛋白的磷酸化作用,并研究HMG蛋白翻译后修饰的生物学意义。由于对组蛋白翻译后修饰的研究已经为转录机制带来了丰富的新见解,我们预计,对HMG蛋白翻译后修饰的全面表征将为更好地理解这些非组蛋白染色体蛋白在转录调控和癌症发展中的作用铺平道路。此外,所提出的研究结果可能为癌症诊断和预后提供重要的分子生物标志物。
英文摘要
DESCRIPTION (provided by applicant): The long-term goal of this project is to understand the biological implications of the post-translational modifications of non-histone chromosomal high-mobility group (HMG) proteins. The HMG proteins are recognized as general transcription factors and they can adopt a number of post-translational modifications including phosphorylation, methylation, acetylation and glycosylation. Our hypothesis is that not only the expression, but also the post-translational modifications of HMG proteins, are correlated with cancer progression and malignant transformation. To test this hypothesis, we propose experiments according to the following specific aims: Aim 1, to examine systematically the post-translational modifications of HMG proteins in both normal and cancer cells; Aim 2, to investigate whether the level of expression and the nature of the post-translational modifications of HMG proteins are correlated with cancer progression; Aim 3, to study the phosphorylation of HMG proteins by purified protein kinase in vitro and to examine the biological implications of the post-translational modifications of HMG proteins. As studies on histone post-translational modifications have led to a wealth of new insights into the mechanisms of transcription, we anticipate that a thorough characterization of the post-translational modifications of HMG proteins will pave the way for a better understanding of the role of these non-histone chromosomal proteins on transcriptional regulation and cancer development. In addition, the outcome of proposed studies may provide important molecular biomarkers for cancer diagnosis and prognosis.
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