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CONTROL OF TRANSCRIPTION IN EUKARYOTIC CELLS

CONTROL OF TRANSCRIPTION IN EUKARYOTIC CELLS
真核细胞转录的控制
批准号:
2444517
负责人:
Donal Luse
金额:
$28.0万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1981
资助国家:
美国
项目状态:
已结题
起止时间:
1981-07-01 至 2000-06-30

项目摘要

项目成果

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相关文献

中文摘要
翻译
为了充分了解真核生物基因表达的调控
英文摘要
In order to fully understand the control of gene expression in eukaryotic cells, it is necessary to achieve a much greater understanding of the RNA synthesis machinery, which is one of the most important targets for regulatory pathways. It is now known that RNA polymerase Il, which synthesizes all protein-encoding RNAs, is subject to control at many points: at the assembly of the initiation complex. at the transition into elongation and at discrete arrest sites during the elongation process. Our long-term goal is to provide answers to two fundamental questions: first, what are the molecular events that accompany the transition of RNA polymerase II from the unstable, initiating state to the stable elongation state, and second, what changes in the RNA polymerase II elongation complex are responsible for the loss of elongation competence during arrest? In order for the RNA polymerase to successfully pass from the preinitiation complex to stable transcript elongation, it must escape from an abortive initiation pathway and begin translocation down the template. Simplified systems for transcription initiation will be employed to study the sequence and factor requirements for successful escape from abortive initiation. We will also make a comparison of structural parameters among a series of complexes which are passing through the initiation-elongation transition, in order to identify structural changes which accompany the conversion to elongation competence. A similar series of experiments are proposed to study the transitions that accompany loss of the ability to elongate during arrest; in this case we hope to identify structural features distinctive to the arrested state. To accompany this latter study we will attempt to define more fully the sequence signals that cause arrest. We will also extend earlier studies into the molecular mechanisms of recovery from arrest, in order to better understand the transcript cleavage/resynthesis reaction which is required for recovery.
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The effect of nucleosomes on the earliest stages of RNA polymerase II transcription
TRANSCRIPTION OF CHROMATIN TEMPLATES
  • 批准号:
    6526056
  • 项目类别:
  • 资助金额:
    $29.3万
  • 财政年份:
    1999
  • 负责人:
    Donal Luse
  • 依托单位:
TRANSCRIPTION OF CHROMATIN TEMPLATES
  • 批准号:
    2883938
  • 项目类别:
  • 资助金额:
    $27.25万
  • 财政年份:
    1999
  • 负责人:
    Donal Luse
  • 依托单位:
TRANSCRIPTION OF CHROMATIN TEMPLATES
  • 批准号:
    6182028
  • 项目类别:
  • 资助金额:
    $28.0万
  • 财政年份:
    1999
  • 负责人:
    Donal Luse
  • 依托单位:
海外基金