Molecular Cell and Analyitical Services Facility Core
分子细胞和分析服务设施核心
基本信息
- 批准号:9040176
- 负责人:
- 金额:$ 14.98万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:
- 资助国家:美国
- 起止时间:至 2017-05-31
- 项目状态:已结题
- 来源:
- 关键词:Air PollutionApoptosisBioinformaticsBiological AssayCandidate Disease GeneCarcinogensCell CycleCellsCellular biologyConsultationsCore FacilityCulture MediaDNADNA MethylationDNA SequenceDataDiseaseDocumentationDoseEducationEducational workshopEmerging TechnologiesEnvironmentEnvironmental ExposureEnvironmental HealthEpigenetic ProcessEquipmentEvolutionFlow CytometryFluorescenceFluorescence Resonance Energy TransferFundingFunding AgencyGelGene ExpressionGenesGenomeGenomicsHealthHousingHumanHuman GenomeImageryImmune responseMetalsMethodologyMethylationMicroscopyMolecularMolecular BiologyMolecular Biology TechniquesOrganismOzoneParticulatePathway AnalysisPathway interactionsPlayPreparationPreventive InterventionReagentResearchResearch PersonnelResearch SupportResourcesRoentgen RaysRoleSentinelServicesSignal PathwaySignal TransductionSiteTechniquesTechnologyTestingTherapeutic InterventionTimeTissuesToxic Environmental SubstancesTrainingTraining and EducationWorkYeastsabsorptionbiomarker discoverycost efficientdesigndiscountenvironmental agentenvironmental stressorepigenetic regulationepigenomeepigenomicsfetal bovine serumgene environment interactioninstrumentinterdisciplinary approachmammalian genomememberpredictive markerprotein expressionpyrosequencingresearch studyresponsestatisticstissue culturetooltranscriptometranscriptome sequencingtrendwhole genome
项目摘要
The overall objective of the Molecular Cell and Analytical Services Facility Core (MCASFC) is to provide
Center members with education on, and access to, state-of-the-art tools for assessing the effects of the
environment on human and mammalian genomes and epigenomes. The Core also provides analytical
services, particularly those for metals analysis in cells and tissues of exposed organisms, since metal effects
on the genome and epigenome are specialized research strengths of the Center. The rationale for, and
continuing evolution of, this Core reflects current trends in environmental health research, and in particular the
rapidly changing field of gene x environment interactions. Functionally important, dose-related perturbations to
human health from environmental stressors (e.g. metals, carcinogens, air pollution particulates) are being
actively analyzed by Center researchers who study changes in gene expression, epigenetic regulation at
candidate gene and whole genome levels, cell cycle perturbations, protein expression and signaling pathway
interactions. The MCASFC supports Center investigators' funded studies using genomics and epigenomics to
identify biomarkers and predictive sentinels of toxic challenges to health, as well as to identify targets for
preventive and therapeutic interventions. One new initiative implemented in 2008 and overseen by this core is
the collaborative yeast screen project involving analysis of global gene expression changes induced by metals
and ozone. This new project, supported in part by the Center Director's fund, involved multiple Center
investigators with Dr. Thomas Begley at the GeNYsis Center in Albany, NY. It has become increasingly
evident that the epigenome plays an enormous role in modulating the responses of organisms to
environmental exposures. Thus, other new initiatives that have developed for this Core since the last renewal
are the incorporation of ChlP-Chip, ChlP-Seq and RNA-Seq for epigenetic and transcriptome biomarker
discovery and for investigating mechanisms underlying toxic and disease responses to environmental agents.
Research on genome/epigenome x environment interactions requires multidisciplinary approaches and
utilization of highly sensitive molecular techniques supported by state-of-the-art instruments and emerging
technologies. The MCASFC provides Center investigators with evolving access to specialized methodologies
and equipment, either on-site or off-site, by taking advantage of regional resources involving intra- and interuniversity
research partnerships. The MCASFC acquires new equipment as deemed necessary, by continuing
to leverage funds from competitive and institutional funding sources. Furthermore, since genome/epigenome
studies require considerable training prior to implementation, the Facility Core provides Center investigators
with consultation services on the uses, applications, limitations and challenges ofthe latest techniques.
分子细胞和分析服务设施核心(MCASFC)的总体目标是提供
中心成员接受教育,并获得最先进的工具,用于评估
环境对人类和哺乳动物基因组和表观基因组的影响。核心还提供分析
服务,特别是对暴露生物体的细胞和组织中的金属进行分析的服务,
基因组和表观基因组是该中心的专业研究优势。理由,和
该核心的不断演变反映了环境健康研究的当前趋势,特别是
快速变化的基因与环境相互作用领域。功能重要、剂量相关干扰,
环境压力(如金属、致癌物质、空气污染颗粒)对人类健康的影响正在
中心的研究人员积极分析,他们研究基因表达的变化,
候选基因和全基因组水平、细胞周期扰动、蛋白质表达和信号通路
交互. MCASFC支持中心研究人员资助的使用基因组学和表观基因组学的研究,
确定生物标志物和对健康的有毒挑战的预测性哨兵,以及确定目标,
预防和治疗干预。2008年实施并由该核心监督的一项新举措是
协作酵母筛选项目涉及分析金属诱导的全球基因表达变化
和臭氧。这个新项目,部分由中心主任的基金支持,涉及多个中心
研究人员与托马斯贝格利博士在纽约州奥尔巴尼的GeNYsis中心。已变得越来越
显然,表观基因组在调节生物体对
环境暴露。因此,自上次更新以来,
是ChIP-Chip、ChIP-Seq和RNA-Seq的掺入,用于表观遗传和转录组生物标志物
发现和调查机制潜在的毒性和疾病的反应,环境因素。
基因组/表观基因组x环境相互作用的研究需要多学科的方法,
利用高灵敏度的分子技术,由最先进的仪器和新兴的
技术. MCASFC为中心研究人员提供不断发展的专业方法
和设备,无论是现场或场外,通过利用区域资源,涉及内部和大学间
研究伙伴关系。MCASFC在认为必要时购买新设备,
从竞争性和机构资金来源筹集资金。由于基因组/表观基因组
研究在实施前需要大量培训,设施核心为中心研究者提供
就最新技术的使用、应用、局限性和挑战提供咨询服务。
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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Max Costa其他文献
Max Costa的其他文献
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{{ truncateString('Max Costa', 18)}}的其他基金
Persistent transcriptional changes induced by nickel through epigenetic alterations
镍通过表观遗传改变诱导持续转录变化
- 批准号:
10077549 - 财政年份:2020
- 资助金额:
$ 14.98万 - 项目类别:
Persistent transcriptional changes induced by nickel through epigenetic alterations
镍通过表观遗传改变诱导持续转录变化
- 批准号:
9899647 - 财政年份:2020
- 资助金额:
$ 14.98万 - 项目类别:
Persistent transcriptional changes induced by nickel through epigenetic alterations
镍通过表观遗传改变诱导持续转录变化
- 批准号:
10515635 - 财政年份:2020
- 资助金额:
$ 14.98万 - 项目类别:
Persistent transcriptional changes induced by nickel through epigenetic alterations
镍通过表观遗传改变诱导持续转录变化
- 批准号:
10294236 - 财政年份:2020
- 资助金额:
$ 14.98万 - 项目类别:
Arsenic and Nickel Carcinogenesis in Human Lung Cells
砷和镍对人肺细胞的致癌作用
- 批准号:
10470848 - 财政年份:2019
- 资助金额:
$ 14.98万 - 项目类别:
MEG3 deletion drives lung tumorigenesis due to environmental nickel exposure
由于环境镍暴露,MEG3 缺失导致肺部肿瘤发生
- 批准号:
9852426 - 财政年份:2019
- 资助金额:
$ 14.98万 - 项目类别:
Arsenic carcinogenesis and disruption of histone variant H3.3 assembly
砷致癌和组蛋白变体 H3.3 组装的破坏
- 批准号:
10407027 - 财政年份:2019
- 资助金额:
$ 14.98万 - 项目类别:
Arsenic and Nickel Carcinogenesis in Human Lung Cells
砷和镍对人肺细胞的致癌作用
- 批准号:
10004646 - 财政年份:2019
- 资助金额:
$ 14.98万 - 项目类别:
Arsenic carcinogenesis and disruption of histone variant H3.3 assembly
砷致癌和组蛋白变体 H3.3 组装的破坏
- 批准号:
10631227 - 财政年份:2019
- 资助金额:
$ 14.98万 - 项目类别:
Arsenic and Nickel Carcinogenesis in Human Lung Cells
砷和镍对人肺细胞的致癌作用
- 批准号:
10681242 - 财政年份:2019
- 资助金额:
$ 14.98万 - 项目类别:
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