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DEVELOPMENT OF TRANSLATION STATE ARRAY ANALYSIS

DEVELOPMENT OF TRANSLATION STATE ARRAY ANALYSIS
平移状态数组分析的发展
批准号:
6619630
负责人:
DAVID R MORRIS
金额:
$73.91万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-02-08 至 2005-01-31

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中文摘要
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英文摘要
DESCRIPTION: (Applicant's Description) With the rapidly expanding availability of entire genome sequences, the potential for analyzing whole-genome expression patterns is attaining reality. The availability of this vast pool of comparative data will have a major impact on cancer research. Clearly, however, the success of these approaches depends critically on being able to define the relationship between expression patterns and downstream events that define phenotype. For the most part, these downstream events are mediated by the biological activities of protein molecules, which are in turn controlled by protein level and post-translational modification. In this application, we propose to develop a second generation scheme for mRNA expression analysis. In order to develop this technology and at the same time generate biologically important information, we have chosen as our model cell-cycle regulation of gene expression in the yeast Saccharomyces cerevisiae. The core technology in this proposal is what we have termed translation state array analysis (TSSA). TSSA provides, in addition to the absolute levels of individual mRNA molecules, information on the degree to which these mRNAs are engaged in protein synthesis. The results from TSAA will be correlated with datasets generated from proteomic analysis. Combining these three measurements (total mRNA, translated mRNA and protein level) from the same biological system will enable us to make statements about detailed mechanisms of regulation of specific genes and also identify clusters of genes that are regulated through the same mechanisms. This study will provide more finely honed high-throughput tools to provide insight into both mechanisms of regulation of individual genes and the levels and activities of the proteins that ultimately dictate phenotype.
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Dynamic model of the process of protein synthesis in eukaryotic cells.
真核细胞蛋白质合成过程的动态模型。
DOI: 10.1007/s11538-006-9128-2
发表时间: 2007
期刊: Bulletin of mathematical biology
影响因子: 3.5
作者: [Skjondal-Bar,Nadav, Morris,DavidR]
通讯作者: Morris,DavidR
Application of RiboTag-seq to Exploration of Tumor Microenvironments
  • 批准号:
    7852730
  • 项目类别:
  • 资助金额:
    $85.0万
  • 财政年份:
    2009
  • 负责人:
    DAVID R MORRIS
  • 依托单位:
Application of RiboTag-seq to Exploration of Tumor Microenvironments
  • 批准号:
    7943953
  • 项目类别:
  • 资助金额:
    $87.66万
  • 财政年份:
    2009
  • 负责人:
    DAVID R MORRIS
  • 依托单位:
Functions of the FMRP Isoforms
  • 批准号:
    7707256
  • 项目类别:
  • 资助金额:
    $15.28万
  • 财政年份:
    2008
  • 负责人:
    DAVID R MORRIS
  • 依托单位:
Cell-specific Transcript Profiling in Complex Tissues
  • 批准号:
    7295761
  • 项目类别:
  • 资助金额:
    $22.72万
  • 财政年份:
    2006
  • 负责人:
    DAVID R MORRIS
  • 依托单位:
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