课题基金 / 基金详情

Diapause regulation and stress tolerance in artemia embryos: gene expression, protein function and metabolism

Diapause regulation and stress tolerance in artemia embryos: gene expression, protein function and metabolism
卤虫胚胎的滞育调节和应激耐受性:基因表达、蛋白质功能和代谢
批准号:
7661-2011
负责人:
MacRae, Thomas
金额:
$3.5万
依托单位:
依托单位国家:
加拿大
项目类别:
Discovery Grants Program - Individual
财政年份:
2014
资助国家:
加拿大
项目状态:
已结题
起止时间:
2014-01-01 至 2015-12-31

项目摘要

项目成果

MacRae, Thomas的其他基金

相似基金

相关文献

中文摘要
翻译
甲壳类动物卤虫的胚胎可以发育成游泳的幼虫,或者它们可以包囊并进入滞育,滞育是一种以发育停滞和代谢活动大大降低为特征的生理状态。包被的胚胎具有极强的抗应激能力,即使在环境温度下水合,它们也能在高温、干燥和多年的缺氧中存活。因此,被包囊的卤虫胚胎代表了地球上最具抗应激能力的后生动物生命形式之一。卤虫胚胎在滞育发育过程中表现出差异基因表达,产生启动所需的蛋白质。维持或者终止滞育。这项工作的长期目标是阐明卤虫胚胎调节滞育特异性发育的细胞、分子和生化机制,并确定胚胎如何在生理应激下生存。短期目标包括鉴定滞育期间上调的基因,并确定其蛋白质项目的功能。特别令人感兴趣的是丰富的分子伴侣,如滞育特异性小热休克蛋白和铁蛋白同系物artemin。其他感兴趣的蛋白质的例子包括那些介导细胞内信号传导途径,影响代谢活动,细胞生长和分裂,基因转录。调节滞育终止的蛋白质变化也将被确定,这是一个几乎未被触及的领域。这些结果将有助于我们理解真核细胞在发育过程中和暴露于压力下的基本过程。所获得的信息将在医学上有潜在的应用,因为小的热休克蛋白功能的扰动会导致疾病。此外,许多经历滞育的昆虫通过其作为害虫的作用影响农业和林业,卤虫作为水产养殖的饲料来源发挥着重要作用。
英文摘要
Embryos of the crustacean, Artemia franciscana, may develop into swimming larvae or they may encyst and enter diapause, a physiological state characterized by developmental arrest and greatly reduced metabolic activity. Encysted embryos are extremely stress tolerant and they survive high temperature, desiccation and years of anoxia even when hydrated at ambient temperature. As such, encysted Artemia embryos represent one of the most stress resistant metazoan life forms on earth. Artemia embryos exhibit differential gene expression during diapause-destined development which yields proteins required for initiation. maintenance and perhaps termination of diapause. The long term objectives of the work are to elucidate cell, molecular and biochemical mechanisms by which Artemia embryos regulate diapause-specific development and to determine how embryos survive physiological stress. Short term objectives include the identification of genes that are up-regulated during diapause and determining the functions of their protein projects. Of particular interest are abundant molecular chaperones such as the diapause-specific small heat shock proteins and the ferritin homologue artemin. Other examples of interesting proteins include those mediating intracellular signalling pathways which influence metabolic activity, cell growth and division, and gene transcription. Protein changes that regulate diapause termination, a field that is almost untouched, will also be identified. The results will contribute to our apreciation of fundamental processes in eukaryotic cells during development and upon exposure to stress. The information obtained will have potential applications in medicine as perturbation of small heat shock protein function leads to disease. Additionally, many insects that undergo diapause influence agriculture and forestry through their roles as pests and Artemia has an important role as a source of feed in aquaculture.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Diapause, Stress Tolerance and Molecular Chaperones in Artemia franciscana
  • 批准号:
    RGPIN-2016-04882
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $3.93万
  • 财政年份:
    2018
  • 负责人:
    MacRae, Thomas
  • 依托单位:
Diapause, Stress Tolerance and Molecular Chaperones in Artemia franciscana
  • 批准号:
    RGPIN-2016-04882
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $3.93万
  • 财政年份:
    2017
  • 负责人:
    MacRae, Thomas
  • 依托单位:
Diapause, Stress Tolerance and Molecular Chaperones in Artemia franciscana
  • 批准号:
    RGPIN-2016-04882
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $3.93万
  • 财政年份:
    2016
  • 负责人:
    MacRae, Thomas
  • 依托单位:
Diapause regulation and stress tolerance in artemia embryos: gene expression, protein function and metabolism
  • 批准号:
    7661-2011
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $3.5万
  • 财政年份:
    2015
  • 负责人:
    MacRae, Thomas
  • 依托单位:
国内基金
海外基金
糖尿病ED中成纤维细胞衰老调控内皮细胞线粒体稳态失衡的机制研究
  • 批准号:
    82371634
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    赵福军
  • 依托单位:
PRNP调控巨噬细胞M2极化并减弱吞噬功能促进子宫内膜异位症进展的机制研究
  • 批准号:
    82371651
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    赵栋
  • 依托单位:
CBP/p300-HADH轴在基础胰岛素分泌调节中的作用和机制研究
  • 批准号:
    82370798
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    王晓
  • 依托单位:
精氨酸调控骨髓Tregs稳态在脓毒症骨髓功能障碍中的作用研究
  • 批准号:
    82371770
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    宁铂涛
  • 依托单位: