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Collaborative Research: The impact of reproduction on the tempo and pattern of mitonuclear adaptation

Collaborative Research: The impact of reproduction on the tempo and pattern of mitonuclear adaptation
合作研究:繁殖对线粒体核适应速度和模式的影响
批准号:
2232413
负责人:
Suzanne Estes
金额:
$46.95万
依托单位:
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2022
资助国家:
美国
项目状态:
已结题
起止时间:
2022-06-01 至 2024-07-31

项目摘要

项目成果

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中文摘要
翻译
该项目旨在了解细胞核和线粒体基因组如何促进适应性进化,并识别有性生殖对这一过程的影响。大多数非微生物生命形式的细胞含有大量线粒体,负责产生生物能量的细胞器。线粒体包含自己的基因组,它们远小于“常规”核基因组,编码一组与能量代谢相关的独特基因。正常的线粒体功能依赖于核基因组编码的许多基因产物。因此,这两个基因组必须协同进化;即,线粒体共同进化这项研究将提供第一个全面评估核和线粒体基因组变化伴随控制,适应性进化在不同的生殖系统。它还将导致发现新的突变,抑制线粒体损伤的影响。该项目将为科学界提供重要的数据和资源,扩大项目执行人的教育和外联活动,并为一名博士后研究员、一名研究技术人员以及研究生和本科生提供研究培训和专业发展。线粒体基因组的分析长期以来一直用于法医和系统发育应用,线粒体基因组的缺陷与大约1,000种人类遗传疾病、癌症和衰老有关。线粒体遗传学和线粒体相互作用对生物学研究的各个领域的核心重要性表明,这项研究将产生深远的影响。这项研究将提供第一个直接的,非回顾性的主要假设来解释线粒体基因组共同进化的测试。该项目将应用秀丽隐杆线虫的实验基因组学来研究线粒体电子传递链(ETC)背景下的进化过程,其正常功能依赖于维持有利的线粒体上位相互作用。该项目将:1)确定性系统对线粒体适应的克里思和模式的影响。C.含有有害的线粒体和核编码的ETC突变的线虫菌株将在经历专性自交、兼性异交或专性异交的复制群体中经历适应,以及2)确定个体线粒体突变的进化动力学、功能特征和性别特异性效应。基因组学、生物信息学和表型分析将确定线粒体和核突变的分子基础和功能基础,以掩盖有害的ETC突变的影响,并揭示异交率和线粒体适应之间的关系。该奖项反映了NSF的法定使命,并被认为值得通过使用基金会的智力价值和更广泛的影响审查标准进行评估来支持。
英文摘要
This project aims to understand how nuclear and mitochondrial genomes contribute to adaptive evolution, and to discern the impact of sexual reproduction on this process. The cells of most non-microbial life forms contain numerous mitochondria, organelles responsible for generating biological energy. Mitochondria contain their own genomes, which are far smaller than "regular" nuclear genomes and encode a unique set of genes related to energy metabolism. Proper mitochondrial functioning relies upon many gene products encoded by the nuclear genome. These two genomes must therefore evolve in concert; i.e., mitonuclear coevolution. This research will provide the first comprehensive assessment of nuclear and mitochondrial genomic change accompanying controlled, adaptive evolution under different reproductive systems. It will also result in discovery of novel mutations that suppress the effects of mitonuclear damage. The project will provide important data and resources to the scientific community, expand the PIs' educational and outreach activities, and provide research training and professional development for a postdoctoral fellow, a research technician, and graduate and undergraduate students. Analysis of mitochondrial genomes has long been used for forensic and phylogenetic applications, and defects in mitochondrial genomes are implicated in approximately 1,000 human genetic diseases, cancer and aging. The central importance of mitochondrial genetics and mitonuclear interaction to diverse areas of biological research suggest that this research will have far-reaching impacts.This research will provide the first direct, non-retrospective tests of major hypotheses to explain mitonuclear genome coevolution. The project will apply experimental genomics with Caenorhabditis elegans nematodes to study evolutionary process within the context of the mitochondrial electron transport chain (ETC), the proper functioning of which relies on the maintenance of favorable mitonuclear epistatic interactions. The project will: 1) Determine the impact of sexual system on the tempo and patterns of mitonuclear adaptation. C. elegans strains containing deleterious mitochondrial- and nuclear-encoded ETC mutations will undergo adaptation in replicate populations experiencing obligate selfing, facultative outcrossing, or obligate outcrossing, and 2) Determine the evolutionary dynamics, functional characteristics and sex-specific effects of individual mitonuclear mutations. Genomic, bioinformatic and phenotypic analyses will determine the molecular bases and functional underpinnings of mitochondrial and nuclear mutations available to mask the effects of deleterious ETC mutations, and reveal the relationship between rates of outcrossing and mitonuclear adaptation.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
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Collaborative Research: The impact of reproduction on the tempo and pattern of mitonuclear adaptation
  • 批准号:
    1817993
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $45.97万
  • 财政年份:
    2018
  • 负责人:
    Suzanne Estes
  • 依托单位:
Mitonuclear Interaction and the Genetic Architecture of Phenotypic Evolution
  • 批准号:
    1330427
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $75.0万
  • 财政年份:
    2013
  • 负责人:
    Suzanne Estes
  • 依托单位:
Evolutionary Paths of Compensatory Mutations in Genetic Networks
  • 批准号:
    0743871
  • 项目类别:
    Standard Grant
  • 资助金额:
    $0.0万
  • 财政年份:
    2008
  • 负责人:
    Suzanne Estes
  • 依托单位:
Research Starter Grant
  • 批准号:
    0625211
  • 项目类别:
    Standard Grant
  • 资助金额:
    $0.0万
  • 财政年份:
    2006
  • 负责人:
    Suzanne Estes
  • 依托单位:
国内基金
海外基金
Research on Quantum Field Theory without a Lagrangian Description
  • 批准号:
    24ZR1403900
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    SATOSHI NAWATA
  • 依托单位:
Cell Research
Cell Research
Cell Research (细胞研究)