POSTTRANSLATIONAL MODIFICATIONS ON HISTONES AND HISTONE VARIANTS
POSTTRANSLATIONAL MODIFICATIONS ON HISTONES AND HISTONE VARIANTS
批准号:
8169757
负责人:
BARBARA PANNING
金额:
$0.35万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-12 至 2011-05-31
关键词:
AcetylationCellsChromatinChromatin StructureComputer Retrieval of Information on Scientific Projects DatabaseDevelopmentEpigenetic ProcessFundingGene ExpressionGeneticGrantHistonesInstitutionLeadMaintenanceMalignant NeoplasmsMemoryMethylationModificationNatureOrganismPatternPhosphorylationPost-Translational Protein ProcessingResearchResearch PersonnelResourcesRoleSourceSpecificityUbiquitinationUnited States National Institutes of HealthVariantcell typecombinatorialflexibilityprogramstandem mass spectrometry
中文摘要
这个子项目是许多研究子项目中利用
资源由NIH/NCRR资助的中心拨款提供。子项目和
调查员(PI)可能从NIH的另一个来源获得了主要资金,
并因此可以在其他清晰的条目中表示。列出的机构是
该中心不一定是调查人员的机构。
多细胞生物由具有相同遗传信息但高度分化的各种细胞类型组成,每种细胞类型具有独特的基因表达模式。建立和维持这些不同的表达模式对细胞特性和生物生存至关重要,单个细胞中的异常基因表达可能导致发育异常或癌症。表观遗传调控机制利用染色质结构的动态改变,如组蛋白甲基化、乙酰化、磷酸化和泛素化,来调节基因的表达。这些翻译后修饰以组合的方式整合在一起,为细胞提供转录记忆,以在许多分裂中稳定地维持基因表达模式,并提供发育灵活性,以促进基因表达的程序性改变。利用串联质谱仪提供的前所未有的灵敏度和结构特异性,我们希望阐明哺乳动物染色质中丰富的表观遗传信息的性质和功能作用。
英文摘要
This subproject is one of many research subprojects utilizing the
resources provided by a Center grant funded by NIH/NCRR. The subproject and
investigator (PI) may have received primary funding from another NIH source,
and thus could be represented in other CRISP entries. The institution listed is
for the Center, which is not necessarily the institution for the investigator.
Multicellular organisms consist of various cell types with the same genetic information but a high degree of differentiation, characterized by a unique pattern of gene expression for each cell type. Establishment and maintenance of these diverse expression patterns is fundamentally important for cell identity and organism survival, and aberrant gene expression in a single cell can lead to developmental abnormalities or cancer. Epigenetic regulatory mechanisms employ dynamic modifications in chromatin structure, such as histone methylation, acetylation, phosphorylation and ubiquitination, to regulate gene expression. These posttranslational modifications are integrated in a combinatorial fashion to provide cells with transcriptional memory to stably maintain gene expression patterns throughout many divisions, and developmental flexibility to facilitate programmed alterations in gene expression. Equipped with the unprecedented sensitivity and structural specificity offered by tandem mass spectrometry, we are hoping to elucidate the nature and functional role of the rich epigenetic information in mammalian chromatin.
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