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Mechanisms of Circadian Rhythmicity in CLOCK-Deficient Mice

Mechanisms of Circadian Rhythmicity in CLOCK-Deficient Mice
时钟缺陷小鼠的昼夜节律机制
批准号:
7131991
负责人:
DAVID Raymond WEAVER
金额:
$36.55万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-06-01 至 2011-05-31

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Circadian rhythms are present in species throughout the animal kingdom. In humans, disorders of circadian timing contribute to circadian-based sleep disorders, maladjustment of shift workers and during jet lag, and may contribute to neuropsychiatric disorders including depression and seasonal affective disorder. A transcriptional-translational feedback loop is at the center of the circadian clock mechanism. The known positive elements driving circadian transcription are CLOCK and BMAL1, two basic helix loop helix proteins that dimerize to activate expression of responsive genes. We have recently generated mice with a null mutation of the Clock gene. Unexpectedly, these CLOCK-deficient mice retain circadian rhythmicity in behavior in constant conditions. Our studies will characterize physiological and molecular rhythms in CLOCK-deficient mice, and assess mechanisms of rhythmicity in the absence of CLOCK. In mice with the previously described dominant negative mutation of Clock, the CLOCK-delta19 protein likely disrupts circadian rhythmicity by interfering with the activity of other key bHLH-PAS proteins, indicating that a major circadian transcriptional activator remains to be identified. A major objective of this project will be to identify this apparent second mechanism for transcriptional activation. We will test the hypothesis that NPAS2, a bHLH-PAS transcription factor closely related to CLOCK, can substitute for CLOCK and thus maintain rhythmicity in CLOCK-deficient mice. We will also determine whether BMAL1 is necessary for rhythmicity in the absence of CLOCK, expecting a finding that will enable studies based on assessment of the functional importance of candidate BMAL1-interacting proteins. The proposed studies are necessary to understand the function of CLOCK, a central component of the circadian clock mechanism, and thus are relevant to understanding and possibly developing novel treatments for circadian-based sleep and psychiatric disorders. In addition, the circadian clock plays diverse roles in regulating reproduction, metabolism, cell growth and tumor progression, so the importance of understanding basic mechanisms of circadian rhythm generation has many implications.
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2010 Pineal Cell Biology Gordon Research Conference
  • 批准号:
    7902655
  • 项目类别:
  • 资助金额:
    $1.2万
  • 财政年份:
    2010
  • 负责人:
    DAVID Raymond WEAVER
  • 依托单位:
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精神分裂症脑网络异常的影像遗传学研究
  • 批准号:
    81000582
  • 项目类别:
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  • 资助金额:
    20.0万元
  • 批准年份:
    2010
  • 负责人:
    刘冰
  • 依托单位:
孤独症全基因组关联第二阶段研究
  • 批准号:
    81071110
  • 项目类别:
    面上项目
  • 资助金额:
    32.0万元
  • 批准年份:
    2010
  • 负责人:
    王力芳
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孤独症与突触发育相关候选基因的关联研究
  • 批准号:
    30870897
  • 项目类别:
    面上项目
  • 资助金额:
    50.0万元
  • 批准年份:
    2008
  • 负责人:
    张岱
  • 依托单位:
用dsDNA微阵列筛选NF-κB DNA靶点及靶基因
  • 批准号:
    60871014
  • 项目类别:
    面上项目
  • 资助金额:
    35.0万元
  • 批准年份:
    2008
  • 负责人:
    王进科
  • 依托单位: