FASEB SRC on Biological Methylation: From DNA and Histones to Disease
FASEB SRC 关于生物甲基化:从 DNA 和组蛋白到疾病
基本信息
- 批准号:8316960
- 负责人:
- 金额:$ 1.1万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2012
- 资助国家:美国
- 起止时间:2012-08-06 至 2013-07-31
- 项目状态:已结题
- 来源:
- 关键词:AmericanAreaBindingBiochemistryBiologicalBiological ProcessBiologyCell physiologyChemicalsCollaborationsColoradoDNADNA DamageDNA MethylationDNA MethyltransferaseDNA Modification MethylasesDevelopmentDiseaseEducational workshopEnzymatic BiochemistryEpigenetic ProcessEvolutionFundingGene ExpressionGenomeGenome StabilityGenomicsGoalsHistonesHuman DevelopmentIndividualInstitutionMalignant NeoplasmsMethionineMethylationMethyltransferaseModificationParticipantPatternPlayPostdoctoral FellowProtein MethyltransferasesProteinsReadingRequest for ProposalsResearchResearch PersonnelRoleRunningS-AdenosylmethionineScienceScientistSenior ScientistSeriesSignal TransductionSocietiesStructureTechnologyTimeTranscriptional Regulationabstractingbasedemethylationdesignenzyme mechanismgraduate studenthuman diseaseinhibitor/antagonistinterestmacromoleculemalignant neurologic neoplasmsmeetingsnervous system disorderpluripotencypostersprogramsresearch and developmentresponsesmall moleculesymposium
项目摘要
DESCRIPTION (provided by applicant): This application seeks partial support for the 2012 Federation of American Societies for Experimental Biology (FASEB) Summer Research Conference on "Biological Methylation: From DNA and Histones to Disease". This will be the tenth biennial conference on this topic and will be held from August 12-17, 2012 at the Silvertree Hotel in Snowmass, CO. The "Biological Methylation" conference has historically taken a unique approach in its integrative coverage of the enzymology, function, and recognition of S-adenosylmethionine-dependent methylation and its influence on diverse biological processes and disease. Over the last sixteen years, this meeting has evolved a particular focus on topics relating to DNA and histone methylation, and the role of these epigenetic modifications in development and disease. Recent advances in the areas of epigenetic reprogramming, which involves the resetting of DNA and histone methylation patterns during development and disease, and the evolution of genome-scale technologies to comprehensively evaluate DNA methylation and histone methylation have put this field at the forefront of modern biology. A major focus of the conference will be the influence of epigenetic (DNA, histone) methylation on gene expression and genome stability, and the contribution of dysregulated methylation to human diseases. New or highlighted in this meeting is an emphasis on epigenetic 'reprogramming', the role of DNA demethylation, environmental influences on the epigenome, and new advances in the field in studying histone/DNA methylation. Other sessions will deal with the structure and function of DNA and protein methyltransferases/demethylases, and the post-translational methylation of non-histone proteins, which has emerged as an exciting new area of study, with central roles in signal transduction, the regulation of transcription and the DNA damage response. We intend to have diverse expertise of the meeting's attendees such that the participants have the opportunity to interact with one another to further advance our understanding of methylation and how methyltransferases and demethylases may be manipulated therapeutically to treat human diseases such as neurological diseases and cancer. The Biological Methylation Conference is attended by a diverse group of junior and senior scientists from a wide range of academic and research institutions in the US and abroad. A major objective of the meeting is to promote interaction between junior scientists (postdoctoral fellows, graduate students, starting investigators) and more senior established investigators. Toward this end, we are including a session entitled "Meet the Experts" - an informal venue designed to permit young scientists an opportunity to meet leaders in the field to talk science and network. The conference format includes eight plenary sessions (48 invited speakers), two "Recent Advances" minisymposia (consisting of 12 speakers selected from submitted abstracts), one Workshop, and two poster sessions. Ample time will be provided for the 120-150 expected participants to socialize and to interact on an informal basis.
PUBLIC HEALTH RELEVANCE: Cellular macromolecules such as DNA and proteins are frequently modified with a small chemical tag called 'methylation'. This modification plays a fundamental role in determining how the genome is packaged and read, and how proteins act together to carry out cellular functions. Patterns of methylation are strictly controlled during development and alterations in epigenetic methylation contribute to human disease, particularly cancer. The proposal requests partial funding for a conference entitled "Biological Methylation: From DNA and Histones to Disease". Approximately 150 scientists will attend to coordinate, exchange, and disseminate information on the underlying mechanisms controlling epigenetic methylation and to explore the contribution of dysregulated methylation to human disease.
描述(由申请人提供):本申请为2012年美国实验生物学学会联合会(FASEB)夏季研究会议“生物甲基化:从DNA和组蛋白到疾病”寻求部分支持。这将是第十届关于这一主题的两年一次的会议,会议将于2012年8月12日至17日在科罗拉多州Snowmass的Silvertree酒店举行。“生物甲基化”会议在历史上采取了独特的方法,在其酶学、功能和s -腺苷蛋氨酸依赖性甲基化的识别及其对多种生物过程和疾病的影响方面进行了综合报道。在过去的16年里,这个会议已经演变成一个特别关注与DNA和组蛋白甲基化有关的主题,以及这些表观遗传修饰在发育和疾病中的作用。表观遗传重编程领域的最新进展,包括在发育和疾病过程中DNA和组蛋白甲基化模式的重置,以及基因组规模技术的发展,以全面评估DNA甲基化和组蛋白甲基化,使这一领域处于现代生物学的前沿。会议的一个主要焦点将是表观遗传(DNA,组蛋白)甲基化对基因表达和基因组稳定性的影响,以及甲基化失调对人类疾病的贡献。本次会议的新的或重点是强调表观遗传“重编程”,DNA去甲基化的作用,环境对表观基因组的影响,以及组蛋白/DNA甲基化研究领域的新进展。其他会议将讨论DNA和蛋白质甲基转移酶/去甲基化酶的结构和功能,以及非组蛋白的翻译后甲基化,这已经成为一个令人兴奋的新研究领域,在信号转导、转录调节和DNA损伤反应中起着核心作用。我们打算让会议与会者有不同的专业知识,这样与会者就有机会相互交流,以进一步推进我们对甲基化的理解,以及甲基转移酶和去甲基化酶如何被用于治疗人类疾病,如神经系统疾病和癌症。生物甲基化会议由来自美国和国外广泛的学术和研究机构的不同群体的初级和高级科学家参加。会议的一个主要目标是促进初级科学家(博士后研究员、研究生、初级研究者)和更资深的研究者之间的互动。为此,我们将包括一个名为“会见专家”的会议,这是一个非正式的场所,旨在让年轻科学家有机会会见该领域的领导人,讨论科学和网络。会议形式包括8场全体会议(48位特邀演讲者)、2场“最新进展”小型专题讨论会(从提交的摘要中选出12位演讲者)、1场研讨会和2场海报会议。将为120-150名预期参与者提供充足的时间进行非正式的社交和互动。
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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Brian D Strahl其他文献
Brian D Strahl的其他文献
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{{ truncateString('Brian D Strahl', 18)}}的其他基金
Mechanisms of chromatin and transcriptional regulation
染色质和转录调控机制
- 批准号:
10395985 - 财政年份:2018
- 资助金额:
$ 1.1万 - 项目类别:
Mechanisms of chromatin and transcriptional regulation
染色质和转录调控机制
- 批准号:
9912773 - 财政年份:2018
- 资助金额:
$ 1.1万 - 项目类别:
Mechanisms of chromatin and transcriptional regulation
染色质和转录调控机制
- 批准号:
10552419 - 财政年份:2018
- 资助金额:
$ 1.1万 - 项目类别:
Mechanisms of chromatin and transcriptional regulation
染色质和转录调控机制
- 批准号:
10582044 - 财政年份:2018
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$ 1.1万 - 项目类别:
Factors that regulate chromatin organization and gene transcription
调节染色质组织和基因转录的因素
- 批准号:
9213378 - 财政年份:2014
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$ 1.1万 - 项目类别:
Factors that regulate chromatin organization and gene transcription
调节染色质组织和基因转录的因素
- 批准号:
9011537 - 财政年份:2014
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A high-throughput approach towards deciphering the histone code
破译组蛋白密码的高通量方法
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8101891 - 财政年份:2008
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7900960 - 财政年份:2008
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$ 1.1万 - 项目类别:
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破译组蛋白密码的高通量方法
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8125465 - 财政年份:2008
- 资助金额:
$ 1.1万 - 项目类别:
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