EXPLOITING MICROBIOME SEQUENCES FOR IMPROVED MODELS OF PROTEIN-DNA INTERACTIONS
EXPLOITING MICROBIOME SEQUENCES FOR IMPROVED MODELS OF PROTEIN-DNA INTERACTIONS
批准号:
8149991
负责人:
GARY D STORMO
金额:
$18.81万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-27 至 2014-06-30
关键词:
AlgorithmsAmino Acid SequenceAreaBacteriaBindingBinding SitesBiologyCharacteristicsChromosomesDNADNA BindingDNA SequenceDNA-Protein InteractionDataData SetDevelopmentFamilyGene ExpressionGene Expression RegulationGenesGraphHelix-Turn-Helix MotifsHumanHuman MicrobiomeHuman bodyIndiumKnowledgeLeadLearningMetagenomicsModelingNucleic Acid Regulatory SequencesOperonPatternPeptide Sequence DeterminationPositioning AttributeProtein Structure DatabasesProteinsResearchSiteSpecificityStructureTestingTherapeuticTrainingWeightbasebiological researchcomputer programdesigngenome sequencingimprovedmembermicrobial communitymicrobiomenovelpromoterpublic health relevancetooltranscription factor
中文摘要
描述(由申请者提供):这个项目将开发计算机程序来开发人类微生物组计划(HMP)DNA序列,以更好地了解DNA-蛋白质相互作用。转录因子及其结合的DNA位点之间的相互作用对控制每个物种内基因的表达至关重要,因此也控制每个物种的特征及其与人类宿主的相互作用。转录因子本身可以很容易地从DNA序列中识别出来,我们将利用这样一个事实,即大多数细菌转录因子调节自身和/或其染色体内的邻近基因。转录因子可以根据研究充分的细菌中类似蛋白质的已知结构,分成几组,预计它们将识别相同的DNA模式。将具有非常相似特异性的蛋白质簇和附近启动子的可能调控区域结合在一起,将为我们提供大量潜在的DNA-蛋白质相互作用位点,在这些位点上应用模式发现算法。这不仅有助于我们了解HMP物种内的调控网络,而且还有助于我们更全面地了解转录因子蛋白和它们识别的DNA模式之间的关系。这将对生物学研究的几个领域产生更广泛的影响,并可能导致设计出具有新特性的新蛋白质,这些蛋白质可能作为研究工具和疗法有用。
与公共健康相关:人类微生物组计划将从居住在人体许多不同微环境中的许多不同物种获得DNA序列。该项目将开发计算机程序来分析这些DNA序列,以帮助发现这些物种中基因的表达是如何调控的。基因表达的调控是理解微生物群落和人类宿主之间相互作用的关键因素。
英文摘要
DESCRIPTION (provided by applicant): This project will develop computer programs to exploit the Human Microbiome Project (HMP) DNA sequences to better understand DNA-protein interactions. The interactions between transcription factors and the DNA sites that they bind to are critical to controlling the expression of the genes within each species, and therefore also the characteristics of each species and its interactions with the human host. The transcription factors themselves can be readily identified from DNA sequences and we will take advantage of the fact that most bacterial transcription factors regulate themselves and/or adjacent genes within their chromosomes. Transcription factors can be clustered into groups that are expected to recognize the same patterns of DNA, based on known structures for similar proteins from well studied bacteria. Together the clusters of proteins with very similar specificity and the probable regulatory regions of nearby promoters will give us a very large number of potential DNA-protein interacting sites on which to apply pattern discovery algorithms. This should not only help us to learn about the regulatory networks within the HMP species, but also lead to more general understanding about the relationships between transcription factor proteins and the DNA patterns that they recognize. This will have broader implications across several areas of biological research and may lead to the design of new proteins with novel specificities that could be useful as research tools and for therapeutics.
PUBLIC HEALTH RELEVANCE: The Human Microbiome Project will obtain DNA sequences from many different species inhabiting many different microenvironments of the human body. This project will develop computer programs to analyze those DNA sequences to help discover how the expression of the genes in those species is regulated. The regulation of gene expression is a key element in understanding the interactions between the microbial communities and the human host.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
Corrigendum to: Spec-seq: determining protein-DNA-binding specificity by sequencing.
勘误表:Spec-seq:通过测序确定蛋白质-DNA 结合特异性。
DOI:
10.1093/bfgp/elab044
发表时间:
2022
期刊:
Briefings in functional genomics
影响因子:
4
作者:
[Zuo,Zheng, Chang,YimingKenny, Stormo,GaryD]
通讯作者:
Stormo,GaryD
Single cell tagging of localized RNA from whole populations
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批准号:10266095
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项目类别:
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资助金额:$33.86万
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财政年份:2020
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依托单位:
Single cell tagging of localized RNA from whole populations
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资助金额:$33.86万
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资助金额:$30.49万
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依托单位:
EXPLOITING MICROBIOME SEQUENCES FOR IMPROVED MODELS OF PROTEIN-DNA INTERACTIONS
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批准号:8020738
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项目类别:
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资助金额:$22.8万
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依托单位:
Deciphering the regulatory code of a cell
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财政年份:2007
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依托单位:
Deciphering the regulatory code of a cell
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项目类别:
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财政年份:2007
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负责人:GARY D STORMO
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依托单位:
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项目类别:
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财政年份:2001
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财政年份:2001
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依托单位:
Training Program in Computational Biology
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批准号:7254220
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项目类别:
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财政年份:2001
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依托单位:
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依托单位:
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项目类别:
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资助金额:$15.15万
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财政年份:2001
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负责人:GARY D STORMO
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依托单位:
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项目类别:
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财政年份:2001
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项目类别:
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财政年份:2001
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项目类别:
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资助金额:$17.32万
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财政年份:2001
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负责人:GARY D STORMO
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项目类别:
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项目类别:
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负责人:GARY D STORMO
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依托单位:
海外基金