课题基金 / 基金详情

Novel mtDNA-encoded proteins and mitochondrial sex determination in the Bivalvia (Mollusca)

Novel mtDNA-encoded proteins and mitochondrial sex determination in the Bivalvia (Mollusca)
双壳纲(软体动物)中新型 mtDNA 编码蛋白和线粒体性别决定
批准号:
435656-2013
负责人:
Breton, Sophie
金额:
$2.99万
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:
2018
资助国家:
加拿大
项目状态:
已结题
起止时间:
2018-01-01 至 2019-12-31

项目摘要

项目成果

Breton, Sophie的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
Mitochondria (mt) are known as the "powerhouses of the cell" because they are responsible for most of the energy production in animal cells. They contain their own DNA (mtDNA), which codes for 13 proteins that are involved in energy production. Mutations in mtDNA are responsible for several human diseases including diabetes and cancer. The inheritance of mtDNA in animals has long been believed to be strictly maternal until the discovery of a radically different Doubly Uniparental Inheritance (DUI) system in bivalved mollusks. In DUI, maternal F mtDNA is transmitted to daughters and sons and paternal M mtDNA is transmitted to sons (F vs. M DNA divergence >40%). Breton et al. recently discovered novel (in addition to the typical set of 13) sex-specific mt-encoded proteins in bivalves with DUI, and demonstrated that these proteins are exported from the mitochondria and likely play a role in sex determination. These results are of great value because they show that animal mtDNAs have a larger functional repertoire than previously thought and represent the first case of mtDNA-based sex determination in animals. This challenges textbook biology which state that mt-encoded proteins are uniquely found inside mitochondria to assist in energy production. However, the mechanisms underlying DUI and sex determination are still unknown and the cause of deviation from the strict maternal inheritance rule in bivalves remains an open question. The proposed research aims to better understand (i) the origin and evolution of DUI and the new mt-encoded genes and (ii) the genetic mechanisms that govern DUI and sex determinations in bivalves. This project investigates innovative and potentially transformative ideas in mitochondrial research that will interest a wide range of scientists exploring the fields of organellar inheritance, intergenomic conflict, and evolution of sex determination. It will provide the basis for the development of genetic markers for the manipulation of sex determination for selective breeding programs of economically important bivalves. This work will also shed light on the origin and functions of novel mt-encoded genes and could eventually have medical implications for therapy of mitochondrial diseases. ******************************************************************************************
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Evolutionary Mitochondrial Biology
  • 批准号:
    CRC-2018-00049
  • 项目类别:
    Canada Research Chairs
  • 资助金额:
    $8.74万
  • 财政年份:
    2022
  • 负责人:
    Breton, Sophie
  • 依托单位:
Mitochondrial epigenetics and ORFan genes: exploiting the mitochondrial genetic system to fuel phenotypic variation and functional novelties
  • 批准号:
    RGPIN-2019-04076
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $3.06万
  • 财政年份:
    2022
  • 负责人:
    Breton, Sophie
  • 依托单位:
Mitochondrial epigenetics and ORFan genes: exploiting the mitochondrial genetic system to fuel phenotypic variation and functional novelties
  • 批准号:
    RGPIN-2019-04076
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $3.06万
  • 财政年份:
    2021
  • 负责人:
    Breton, Sophie
  • 依托单位:
Evolutionary Mitochondrial Biology
  • 批准号:
    CRC-2018-00049
  • 项目类别:
    Canada Research Chairs
  • 资助金额:
    $8.74万
  • 财政年份:
    2021
  • 负责人:
    Breton, Sophie
  • 依托单位:
国内基金
海外基金
mtDNA通过非经典途径调控YAP亚细胞定位促进眼表鳞状上皮化生的机制研究
线粒体靶向异质结纳米平台激活 MICU3-VDAC-mtDNA 轴放大 STING 信号促进骨肉瘤免疫治疗研究
  • 批准号:
    2026JJ60295
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2026
  • 负责人:
    鄢祖赟
  • 依托单位:
ACO1介导mtDNA调控基质细胞衰老参与卵巢型内异症纤维化的机制研究
  • 批准号:
    JCZRLH202600430
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2026
  • 负责人:
  • 依托单位:
mtDNA介导的cGAS-STING通路与早发子痫前期发病及围生结局的关联研究