Understanding the Role of Combinatorial Histone PTM Patterns
了解组合组蛋白 PTM 模式的作用
基本信息
- 批准号:8672940
- 负责人:
- 金额:$ 30.4万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2014
- 资助国家:美国
- 起止时间:2014-08-15 至 2018-07-31
- 项目状态:已结题
- 来源:
- 关键词:AFP geneAffectAntibodiesAreaBindingBinding ProteinsBiochemistryBioinformaticsBiologicalBiologyCancer BiologyCellsChemicalsChromatinChromatin StructureDataDevelopmentDevelopmental BiologyDiseaseEctodermEndodermEnvironmentEnzymesEpigenetic ProcessEukaryotaEventFoundationsGene ExpressionGene Expression ProfileGene Expression RegulationGenerationsGenesGenomicsGerm LayersGoalsHealthHistone H3HistonesHumanHuman BiologyInformaticsInvestigationLigationMaintenanceMalignant NeoplasmsMass Spectrum AnalysisMeasurementMediatingMesodermMethodsMolecularMonitorNucleosomesPathologyPatternPhysiologyPlayPluripotent Stem CellsPopulationPost-Translational Modification SitePost-Translational Protein ProcessingProtein FamilyProteinsProteomicsReaderReadingRegenerative MedicineRegulationResearchRoleSignal TransductionSiteSmall Interfering RNATestingTimeTranslatingUndifferentiatedWorkbasebiological researchbiological systemschromatin immunoprecipitationchromatin proteincombinatorialepigenomehuman diseasehuman embryonic stem cellinsightnovelpluripotencyprotein complexpublic health relevanceresearch studyself-renewalstem cell differentiationtooltranscription factor
项目摘要
DESCRIPTION (provided by applicant): Post-translational modifications (PTMs) to histone proteins constitute a major type of epigenetic mechanism that regulates chromatin structure and gene expression patterns in eukaryotes. In addition to their important roles in standard physiology, disruptions in histone PTM signaling patterns have been suggested to be significant, potentially causative factors in various human diseases such as cancer. As most histone PTM work in the chromatin biology field is accomplished using site-specific antibodies, the quantitative measurement of combinational histone PTMs co-occurring on the same molecule has been unmet. Our objectives include the continued development of mass spectrometry-based proteomics and bioinformatic methods for quantitatively interrogating combinatorial histone PTM patterns, and applying these approaches to investigate histone mediated epigenetics mechanisms behind key areas of health related biological research. Here we will specifically apply our approaches to investigate epigenetic histone PTM signaling during human embryonic stem cell differentiation. Our specific aims are three in number and include identifying changing histone PTMs during stem cell differentiation, characterizing combinatorial histone PTM binding protein complexes that translate these PTM patterns, and determining the role of these combinatorial PTMs in maintaining the pluripotent state or facilitating to a specific lineage We expect that these comprehensive proteomic strategies will continue to generate new tools to study epigenetic histone PTMs and generate novel insights into the mechanism of combinatorial histone PTMs in gene regulation during diverse biological events such as cellular differentiation.
描述(申请人提供):组蛋白的翻译后修饰(PTM)构成了真核生物中调节染色质结构和基因表达模式的一种主要表观遗传机制。除了它们在标准生理学中的重要作用外,组蛋白PTM信号模式的中断被认为是各种人类疾病(如癌症)的重要、潜在的致病因素。由于染色质生物学领域中的大多数组蛋白PTM工作都是使用位点特异性抗体来完成的,因此对同一分子上共同存在的组合组蛋白PTM的定量测量一直没有得到满足。我们的目标包括继续开发基于质谱学的蛋白质组学和生物信息学方法来定量询问组合组蛋白PTM模式,并应用这些方法来研究组蛋白介导的表观遗传学机制,其背后是与健康相关的生物学研究的关键领域。在这里,我们将特别应用我们的方法来研究人类胚胎干细胞分化过程中表观遗传学的组蛋白PTM信号。我们的具体目标有三个,包括识别干细胞分化过程中组蛋白PTM的变化,鉴定翻译这些PTM模式的组蛋白PTM结合蛋白复合体,以及确定这些组合PTM在维持多能性状态或促进特定谱系形成中的作用。我们预计,这些综合的蛋白质组策略将继续产生新的工具来研究表观遗传学的组蛋白PTM,并对组合组蛋白PTM在不同生物事件(如细胞分化)的基因调控中的机制产生新的见解。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Benjamin A Garcia其他文献
Microbiota-dependent histone butyrylation in the mammalian intestine
哺乳动物肠道中微生物群依赖性组蛋白丁酰化
- DOI:
10.1101/2022.09.29.510184 - 发表时间:
2022 - 期刊:
- 影响因子:0
- 作者:
Leah A. Gates;B. Reis;P. Lund;M. Paul;M. Leboeuf;Zara Nadeem;T. Carroll;Benjamin A Garcia;D. Mucida;C. Allis - 通讯作者:
C. Allis
Proteotranscriptomic Strategy to Discover Acute Myeloid Leukemia Immunotherapy Targets
- DOI:
10.1182/blood-2022-167378 - 发表时间:
2022-11-15 - 期刊:
- 影响因子:
- 作者:
Lusha Cao;Yang Xu;Tina Glisovic-Aplenc;Kevin Nestler;Saar Gill;Kathrin M. Bernt;Benjamin A Garcia;Hossein Fazelinia;Lingyu Guan;Yi Xing;Richard Aplenc - 通讯作者:
Richard Aplenc
The cerebral cavernous malformation pathway controls embryonic endocardial gene expression through regulation of MEKK3 signaling and KLF expression
脑海绵状血管瘤通路通过调节MEKK3信号和KLF表达来控制胚胎心内膜基因表达
- DOI:
- 发表时间:
2015 - 期刊:
- 影响因子:0
- 作者:
Zinan Zhou;David R. Rawnsley;Lauren M. Goddard;Wei Pan;Xing;Zoltán;Jakus;Hui Zheng;Jisheng Yang;S. Arthur;K. Whitehead;Dean Y Li;Bin;Zhou;Benjamin A Garcia;Xiangjian Zheng;M. Kahn - 通讯作者:
M. Kahn
RNA Modifications on Long Non-Coding RNAs in Multiple Myeloma
- DOI:
10.1182/blood-2024-207137 - 发表时间:
2024-11-05 - 期刊:
- 影响因子:
- 作者:
Catheryn Bolick;Prasanth Thunuguntla;Dakota Colbert;Steve Daly;Yash Rajana;Jaiyana King;Matthew Mueller;Dhanusha Duraiyan;Benjamin A Garcia;John F. DiPersio;Jessica Silva-Fisher - 通讯作者:
Jessica Silva-Fisher
Novel mtDNA Imparts the Connective Tissue Disorder of a Tourette Pedigree
新型线粒体DNA导致抽动秽语症谱系的结缔组织疾病
- DOI:
10.1101/2022.02.25.481696 - 发表时间:
2022 - 期刊:
- 影响因子:0
- 作者:
Patrick M. Schaefer;Leonardo Scherer Alves;M. Lvova;Jessica Huang;K. Rathi;Kevin A. Janssen;Arrienne Butic;T. Yardeni;Ryan M. Morrow;M. Lott;Kierstin N Keller;Benjamin A Garcia;C. Francomano;D. Wallace - 通讯作者:
D. Wallace
Benjamin A Garcia的其他文献
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{{ truncateString('Benjamin A Garcia', 18)}}的其他基金
Quantitative mass spectrometry for comprehending epigenetic mechanisms in a new underlying neurological developmental disorder
定量质谱分析用于理解新的潜在神经发育障碍的表观遗传机制
- 批准号:
10515832 - 财政年份:2022
- 资助金额:
$ 30.4万 - 项目类别:
Quantitative mass spectrometry for comprehending epigenetic mechanisms in a new underlying neurological developmental disorder
定量质谱分析用于理解新的潜在神经发育障碍的表观遗传机制
- 批准号:
10684772 - 财政年份:2022
- 资助金额:
$ 30.4万 - 项目类别:
Viral modulation of epitranscriptomic mechanisms
表观转录组机制的病毒调节
- 批准号:
10317748 - 财政年份:2021
- 资助金额:
$ 30.4万 - 项目类别:
Cocaine-induced histone post-translational modifications
可卡因诱导的组蛋白翻译后修饰
- 批准号:
9304987 - 财政年份:2016
- 资助金额:
$ 30.4万 - 项目类别:
Shared Resources Core 2: Quantitative Proteomics Core
共享资源核心 2:定量蛋白质组学核心
- 批准号:
10269910 - 财政年份:2015
- 资助金额:
$ 30.4万 - 项目类别:
Shared Resources Core 2: Quantitative Proteomics Core
共享资源核心 2:定量蛋白质组学核心
- 批准号:
10024849 - 财政年份:2015
- 资助金额:
$ 30.4万 - 项目类别:
Viral modulation of epitranscriptomic mechanisms
表观转录组机制的病毒调节
- 批准号:
10606522 - 财政年份:2015
- 资助金额:
$ 30.4万 - 项目类别:
Viral modulation of epitranscriptomic mechanisms
表观转录组机制的病毒调节
- 批准号:
10455807 - 财政年份:2015
- 资助金额:
$ 30.4万 - 项目类别:
Viral modulation of epitranscriptomic mechanisms
表观转录组机制的病毒调节
- 批准号:
10407654 - 财政年份:2015
- 资助金额:
$ 30.4万 - 项目类别:
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