Mechanisms of temporal gene regulation in Chlamydia
Mechanisms of temporal gene regulation in Chlamydia
批准号:
8291196
负责人:
Ming Tan
金额:
$37.43万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-08-01 至 2016-06-30
关键词:
BerylliumBindingBiological AssayCellsCenters for Disease Control and Prevention (U.S.)ChlamydiaChlamydia InfectionsChlamydia trachomatisCo-ImmunoprecipitationsCommunicable DiseasesDNA Microarray ChipDNA-Directed RNA PolymeraseDevelopmentDiseaseDisease NotificationEarly PromotersFundingGene ExpressionGene Expression RegulationGenesGenetic TranscriptionGenital systemHistonesHumanIn VitroInfectionLate PromotersLeadMeasuresModelingMolecularOrganismProteinsPublic HealthReportingResistanceSexually Transmitted DiseasesSigma FactorStagingSuperhelical DNATestingTimeTranscriptional RegulationUp-Regulationchromatin immunoprecipitationgenital infectionin vivoinhibitor/antagonistinsightnovelnovel therapeuticspathogenpathogenic bacteriaprematurepreventprogramspromoterselective expressiontooltranscription factor
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): Chlamydia is a pathogenic bacterium with a significant impact on public health. In 2006, more than a million chlamydial infections were reported to the CDC making it the most commonly reported infectious disease. The ability of this organism to cause disease is related to its unusual developmental cycle, which takes place inside a human cell. Our long-term objective is to understand how this pathogen controls the expression of its genes during the developmental cycle so that it can grow and replicate. Our central hypothesis is that the three temporal classes of early, mid and late chlamydial genes are coordinately regulated at the transcriptional level by distinct mechanisms. Aim 1 will determine if the higher levels of chlamydial DNA supercoiling measured in midcycle are used as a general mechanism to upregulate mid genes. Aim 2 will investigate if early genes are selectively expressed at the start of the infection because they are resistant to an inhibitor that prevents transcription of later temporal classes of genes. Aim 3 will examine two regulators that repress late genes to prevent their premature expression. Successful completion of these studies will help us to understand how Chlamydia controls the programmed expression of its genes. These findings may lead to novel therapeutic strategies for treating chlamydial infections by interrupting the developmental cycle.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
A Nanoparticle-Based Multivalent Rotavirus Vaccine
-
批准号:10206373
-
项目类别:
-
资助金额:$62.64万
-
财政年份:2020
-
负责人:Ming Tan
-
依托单位:
Late developmental regulation in Chlamydia
-
批准号:9978694
-
项目类别:
-
资助金额:$44.99万
-
财政年份:2017
-
负责人:Ming Tan
-
依托单位:
Three-dimensional analysis and modeling of the Chlamydia developmental cycle
-
批准号:9207413
-
项目类别:
-
资助金额:$22.25万
-
财政年份:2016
-
负责人:Ming Tan
-
依托单位:
Three-dimensional analysis and modeling of the Chlamydia developmental cycle
-
批准号:9035928
-
项目类别:
-
资助金额:$18.44万
-
财政年份:2016
-
负责人:Ming Tan
-
依托单位:
Norovirus P Particle, A Multifunctional Platform For Vaccine Development
-
批准号:8264954
-
项目类别:
-
资助金额:$19.13万
-
财政年份:2011
-
负责人:Ming Tan
-
依托单位:
Glucose metabolism and ErbB2-mediated cancer progression
-
批准号:8233299
-
项目类别:
-
资助金额:$27.73万
-
财政年份:2011
-
负责人:Ming Tan
-
依托单位:
Norovirus P Particle, A Multifunctional Platform For Vaccine Development
-
批准号:8190929
-
项目类别:
-
资助金额:$22.94万
-
财政年份:2011
-
负责人:Ming Tan
-
依托单位:
Glucose metabolism and ErbB2-mediated cancer progression
-
批准号:9059029
-
项目类别:
-
资助金额:$27.73万
-
财政年份:2011
-
负责人:Ming Tan
-
依托单位:
Glucose metabolism and ErbB2-mediated cancer progression
-
批准号:8448286
-
项目类别:
-
资助金额:$26.07万
-
财政年份:2011
-
负责人:Ming Tan
-
依托单位:
Glucose metabolism and ErbB2-mediated cancer progression
-
批准号:8616726
-
项目类别:
-
资助金额:$26.9万
-
财政年份:2011
-
负责人:Ming Tan
-
依托单位:
Glucose metabolism and ErbB2-mediated cancer progression
-
批准号:8041801
-
项目类别:
-
资助金额:$27.73万
-
财政年份:2011
-
负责人:Ming Tan
-
依托单位:
Molecular mechanisms of gene regulation in Chlamydia
-
批准号:7186703
-
项目类别:
-
资助金额:$9.48万
-
财政年份:2004
-
负责人:Ming Tan
-
依托单位:
Molecular mechanisms of gene regulation in Chlamydia
-
批准号:7373640
-
项目类别:
-
资助金额:$9.48万
-
财政年份:2004
-
负责人:Ming Tan
-
依托单位:
Molecular mechanisms of gene regulation in Chlamydia
-
批准号:6847477
-
项目类别:
-
资助金额:$9.48万
-
财政年份:2004
-
负责人:Ming Tan
-
依托单位:
Molecular mechanisms of gene regulation in Chlamydia
-
批准号:7017102
-
项目类别:
-
资助金额:$9.48万
-
财政年份:2004
-
负责人:Ming Tan
-
依托单位:
Molecular mechanisms of gene regulation in Chlamydia
-
批准号:6705298
-
项目类别:
-
资助金额:$9.48万
-
财政年份:2004
-
负责人:Ming Tan
-
依托单位:
REGULATION OF GENE EXPRESSION IN CHLAMYDIA
-
批准号:6374017
-
项目类别:
-
资助金额:$28.33万
-
财政年份:1999
-
负责人:Ming Tan
-
依托单位:
The Regulation of gene expression in Chlamydia
-
批准号:7255756
-
项目类别:
-
资助金额:$34.66万
-
财政年份:1999
-
负责人:Ming Tan
-
依托单位:
Mechanisms of temporal gene regulation in Chlamydia
-
批准号:8130163
-
项目类别:
-
资助金额:$38.25万
-
财政年份:1999
-
负责人:Ming Tan
-
依托单位:
Mechanisms of Developmental Regulation in Chlamydia
-
批准号:9913440
-
项目类别:
-
资助金额:$45.77万
-
财政年份:1999
-
负责人:Ming Tan
-
依托单位:
国内基金
海外基金
登录
查看更多内容
帽结合蛋白(cap binding protein)调控乙烯信号转导的分子机制
-
批准号:32170319
-
项目类别:面上项目
-
资助金额:58.00万元
-
批准年份:2021
-
负责人:董春海
-
依托单位:
帽结合蛋白(cap binding protein)调控乙烯信号转导的分子机制
-
批准号:--
-
项目类别:--
-
资助金额:58万元
-
批准年份:2021
-
负责人:董春海
-
依托单位:
ID1 (Inhibitor of DNA binding 1) 在口蹄疫病毒感染中作用机制的研究
-
批准号:31672538
-
项目类别:面上项目
-
资助金额:62.0万元
-
批准年份:2016
-
负责人:孙跃峰
-
依托单位:
番茄EIN3-binding F-box蛋白2超表达诱导单性结实和果实成熟异常的机制研究
-
批准号:31372080
-
项目类别:面上项目
-
资助金额:80.0万元
-
批准年份:2013
-
负责人:杨迎伍
-
依托单位:
P53 binding protein 1 调控乳腺癌进展转移及化疗敏感性的机制研究
-
批准号:81172529
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2011
-
负责人:杨其峰
-
依托单位:
DBP(Vitamin D Binding Protein)在多发性硬化中的作用和相关机制的蛋白质组学研究
-
批准号:81070952
-
项目类别:面上项目
-
资助金额:35.0万元
-
批准年份:2010
-
负责人:刘师莲
-
依托单位:
研究EB1(End-Binding protein 1)的癌基因特性及作用机制
-
批准号:30672361
-
项目类别:面上项目
-
资助金额:24.0万元
-
批准年份:2006
-
负责人:徐宁志
-
依托单位: