Center fro Male Reproductive Epigenomics
Center fro Male Reproductive Epigenomics
批准号:
10615596
负责人:
Tong Zhou
金额:
$15.94万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
未结题
起止时间:
2019-09-13 至 2025-03-31
关键词:
3-DimensionalATAC-seqAgeAlkylationAnimal ModelAnimalsArchivesBase SequenceBioinformaticsBiological AssayCell divisionCellsChIP-seqChemicalsChromatinCytosineDNADNA MethylationDNA Modification ProcessDNA SequenceDataData SetDatabasesDetectionDiseaseEnhancersEnvironmentEnzymesEpigenetic ProcessGene ExpressionGene Expression ProfilingGenesGenetic CodeGenetic TranscriptionGenetic studyGenomeGenotypeHi-CHigh-Throughput Nucleotide SequencingHistonesHumanImmunoprecipitationIndividualIntercistronic RegionJournalsLabelLibrariesLife StyleLinkLocationMediatingMetabolicMetabolic DiseasesMethylationMethyltransferaseMissionModificationMusNucleic AcidsNucleotidesOnline SystemsOutsourcingPatternPreparationProcessProteinsRNARNA SequencesResearch PersonnelResourcesRibosomal RNASamplingSeriesServicesSulfhydryl CompoundsTransposaseUnited States National Institutes of HealthUntranslated RNAUpdatebioinformatics toolcell typechromatin modificationcomputational pipelinesdata sharingdesignepigenetic regulationepigenomeepigenomicsgenome browsergenome-widegenomic locushistone modificationhuman subjectinterestintergenerationalmalemethylation patternnext generation sequencingoffspringpreservationpromoterpublic databasereproductivesingle cell analysistranscriptome sequencingtranscriptomicstransgenerational epigenetic inheritancetranslational impacttransmission processuser-friendlyweb server
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Project Summary
While traditional genetic studies to investigate DNA or RNA nucleotide information, epigenetic analyses aim to
characterize chemical modifications within both DNA/RNA sequences and histone proteins. Epigenetic changes
are preserved during cell division and potentially modify the expression of certain genes instead of altering the
genetic code of nucleotide sequences, which is not only due to regular and natural occurrence but also influenced
by several factors including age, the environment/lifestyle, and disease status. More importantly, some
epigenetic modifications can potentially be transmitted to offspring by transgenerational epigenetic inheritance.
Our more recent study suggests that this intergenerational transmission of paternally acquired metabolic
disorders is mediated by a nucleic acid modification enzyme called DNA (cytosine-5-)-methyltransferase 2
(Dnmt2). Inspired by these findings, this P50 will focus on the relationship between epigenetic profiles and
metabolic disorders in both animal models and human subjects. To study the epigenetic regulation, it is critical
to know not only what kinds of modifications are present but also their genomic loci. Therefore, high-throughput
sequencing will be applied to profile epigenetic alterations in both animal and human samples. This Epigenomics
Core (Core D) will provide essential, cutting edge, bioinformatical expertise to facilitate the translational impact
of this highly integrated P50. Firstly, Core D will coordinate outsource library sequencing for individual projects
(Specific Aim #1). Secondly, Core D will provide centralized computational service to store, process, and
analyze the sequencing data, using our in-house well-characterized pipelines (Specific Aims #2). Finally, Core
D will be responsible for hosting an in-house web-based server to share the omics data (Specific Aim #3), which
provides both the internal and external researchers an easy access to the data generated from individual projects.
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Center fro Male Reproductive Epigenomics
-
批准号:10260439
-
项目类别:
-
资助金额:$15.93万
-
财政年份:2019
-
负责人:Tong Zhou
-
依托单位:
Center fro Male Reproductive Epigenomics
-
批准号:10018083
-
项目类别:
-
资助金额:$15.91万
-
财政年份:2019
-
负责人:Tong Zhou
-
依托单位:
国内基金
海外基金
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