Networks, Pathways and Dynamics of Lysine Modification
Networks, Pathways and Dynamics of Lysine Modification
批准号:
8535801
负责人:
Joel S. Bader
金额:
$344.42万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-09-30 至 2016-05-31
关键词:
AcetylationAddressAffectAgingAlgorithmsAllelesAnaphaseAntibodiesAreaAutomobile DrivingBiologicalBiological AssayBiological MarkersBiological ProcessBiologyBiomedical EngineeringBiophysicsBudgetsCell CycleCell Cycle ProgressionCell ProliferationCell physiologyCellsCessation of lifeChemicalsChicagoChromatinClinicalClipCollaborationsComplementComplexDNAData SetDeacetylationDevelopmentDigestionDiploidyDiseaseDissociationElectron TransportEnzymesEpidermal Growth Factor ReceptorEpigenetic ProcessEquilibriumEssential GenesFactor AnalysisFacultyFamilyFatty acid glycerol estersFundingGene ExpressionGene Expression ProfileGene FamilyGenesGeneticGenetic MedicineGenetic RecombinationGenomeGoalsHealthHematoxylin and Eosin Staining MethodHistone DeacetylaseHistone H3Histone H4HistonesHumanHydrolaseImageIn VitroInstitutesInstructionInternshipsIsomerismKineticsKnock-outLeadLearningLibrariesLifeLigandsLung NeoplasmsLysineMalignant neoplasm of lungMapsMarriageMass Spectrum AnalysisMassachusettsMeasurementMeasuresMediatingMemorial Sloan-Kettering Cancer CenterMetabolicMetaphaseMethodsMethylationMicroarray AnalysisMicrofluidic MicrochipsMicrofluidicsMitosisMitoticModificationMolecularMolecular BiologyMolecular GeneticsMonitorMono-SMutateMutationNatural regenerationNatureNeuronsNucleosomesOrganismPathway interactionsPatternPeptide antibodiesPeptidesPharmacologyPhosphorylationPhosphotransferasesPlasticsPlayPost-Translational Protein ProcessingProcessProphaseProtein MicrochipsProtein p53ProteinsProteomeProteomicsPublic Health SchoolsPuerto RicoReadingReagentReceptor ActivationRecombinant DNARegulationRelative (related person)ReporterResearch PersonnelResistanceResourcesRoleRouteSaccharomyces cerevisiaeScienceSeriesSignal PathwaySignal TransductionSirtuinsSister ChromatidSiteSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationStagingStimulusStructureStudentsSubstrate SpecificitySystemTechnologyTemperatureTimeTrainingTriciribine PhosphateUbiquitinUniversitiesWorkYeastsabstractinganalogbasecell typedesignfascinategenetic analysishigh riskhistone modificationin vivoinnovationinteininterestmass spectrometermedical schoolsmembermutantnew technologynovelnovel strategiespre-clinicalprofessorprotein functionreceptorresponsesegregationsmall hairpin RNAsynthetic peptidetechnology developmenttemperature sensitive mutanttool
中文摘要
项目概述(见说明):
英文摘要
PROJECT SUMMARY (See instructions):
Protein modification on histone lysines is critical for controlling gene expression, which itself controls the variable and plastic expression of the proteome in diverse cell types. Modifications on lysine are chemically diverse and include acetylation, methylation, ubiquitylation and sumoylation. We and others have discovered acetyl- and methyl-lysines in many other proteins, and only some directly control gene expression; many are critical regulatory metabolic enzymes. Ubiquitylation controls the life and death of most proteins, and other protein functions. The pathways regulating diverse modifications on lysines are remarkably complex; much remains to be learned. The network of and dynamic interactions among these modification pathways is even more complex; many lysine-modifying proteins are encoded by multi-gene families, have redundant activities, and multiple substrates, only some of which are known. Cross-talk between modifications provides an extra layer of regulation. We have developed genetic, protein chip, chemical, microfiuidic and computational approaches to decrypt and abstract the complex networks defined by these signaling pathways and monitor how they change over time. This proposal extends many unique technologies developed in the last budget period, with a special focus on adapting these technologies to monitoring dynamic proteomic changes occurring in response to a range of biological stimuli. These newer approaches are complemented in this Technology Center for Networks and Pathways by application of innovative mass spectrometry technologies, including sensitive and diverse technologies for quantifying dynamics of lysine modification in cells. The yeast metabolic cycle, integrated with cell cycling and DNA integrity is a fascinating dynamic cycle that will be studied in detail with several of the technologies. Diverse Driving Biological Projects centered on lysine acetylation, methylation, ubiquitylation and SUMOylation, as well as advanced Training efforts. Including an internship for students in Puerto Rico, are integrated with the Technology Development aspects of the proposal. Technologies and resources are actively disseminated via multiple routes; both static and dynamic proteomics datasets will be centrally warehoused/disseminated.
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DOI:
10.1016/j.bbrc.2015.05.077
发表时间:
2015-07-31
期刊:
Biochemical and biophysical research communications
影响因子:
3.1
作者:
[Sahasrabuddhe NA, Huang TC, Kumar P, Yang Y, Ghosh B, Leach SD, Chaerkady R, Pandey A]
通讯作者:
Pandey A
DOI:
10.1002/pmic.201400303
发表时间:
2015-01
期刊:
Proteomics
影响因子:
3.4
作者:
[Pinto SM, Nirujogi RS, Rojas PL, Patil AH, Manda SS, Subbannayya Y, Roa JC, Chatterjee A, Prasad TS, Pandey A]
通讯作者:
Pandey A
DOI:
10.1016/b978-0-12-394395-8.00004-9
发表时间:
2012
期刊:
ADVANCES IN GENETICS
影响因子:
--
作者:
[Zhu, Heng, Qian, Jiang]
通讯作者:
Qian, Jiang
DOI:
10.18632/oncotarget.5020
发表时间:
2015-10-06
期刊:
Oncotarget
影响因子:
--
作者:
[Wu X, Zahari MS, Ma B, Liu R, Renuse S, Sahasrabuddhe NA, Chen L, Chaerkady R, Kim MS, Zhong J, Jelinek C, Barbhuiya MA, Leal-Rojas P, Yang Y, Kashyap MK, Marimuthu A, Ling M, Fackler MJ, Merino V, Zhang Z, Zahnow CA, Gabrielson E, Stearns V, Roa JC, Sukumar S, Gill PS, Pandey A]
通讯作者:
Pandey A
DOI:
10.1093/nar/gkt1251
发表时间:
2014-01
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[Nanjappa V, Thomas JK, Marimuthu A, Muthusamy B, Radhakrishnan A, Sharma R, Ahmad Khan A, Balakrishnan L, Sahasrabuddhe NA, Kumar S, Jhaveri BN, Sheth KV, Kumar Khatana R, Shaw PG, Srikanth SM, Mathur PP, Shankar S, Nagaraja D, Christopher R, Mathivanan S, Raju R, Sirdeshmukh R, Chatterjee A, Simpson RJ, Harsha HC, Pandey A, Prasad TS]
通讯作者:
Prasad TS
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Pathway Discovery and Target Validation for Outgrowth of Breast Cancer Metastases
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Genetic Hotspots for Disease Risk
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A Multidisciplinary Approach to Understanding TB Latency and Reactivation
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Structural, Functional & Evolutionary Genomics Gordon Conference
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Comparative systematic genetics for cardiovascular disease gene identification
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Mapping disease-specific human protein networks
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海外基金