CHARACTERIZATION OF SATB1 MODIFICATIONS FOLLOWING IONIZATION RADIATION
CHARACTERIZATION OF SATB1 MODIFICATIONS FOLLOWING IONIZATION RADIATION
批准号:
7721403
负责人:
Terumi Kohwi-Shigematsu
金额:
$2.4万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-09-08 至 2009-06-30
关键词:
CellsComputer Retrieval of Information on Scientific Projects DatabaseFundingGenesGoalsGrantHistone CodeInstitutionIonizing radiationLaboratoriesModificationNuclearPhosphorylationPost-Translational Protein ProcessingProteinsRadiationRegulator GenesResearchResearch PersonnelResourcesSignal TransductionSourceStagingTestingUnited States National Institutes of Healthcell typeconceptionizationresearch studyresponsethymocyte
中文摘要
这个子项目是众多研究子项目之一
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.
Introduction and Rationale A major goal of my laboratory has been to understand the fundamental mechanisms by which a large body of genes is directed to be either expressed or repressed in a cell-type or stage-specific manner or in response to signals from outside. In this context, we identified a nuclear architectural protein, SATB1, which functions as a global gene regulator. SATB1 is a phosphorylated protein. We wish to test a hypothesis that the SATB1 protein undergoes changes in post-translational modification in irradiated cells. We wish to complete the ongoing collaborative experiment, to determine if there is any change in the phosphorylation status as well as other post-translational modifications, of SATB1 in thymocytes before and after cells are exposed to ionizing radiation. The goal of the project is to assign specific functions to each type of post-translational modification of the SATB1 protein, similar to the concept of the 'histone code.
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会议论文
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