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Contributions of repair outcome choice to establishing the recombination landscape during meiosis

Contributions of repair outcome choice to establishing the recombination landscape during meiosis
修复结果选择对减数分裂期间重组景观的贡献
批准号:
9305097
负责人:
Kimberly Nicole Crown
金额:
$8.13万
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-07-01 至 2018-05-31

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中文摘要
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英文摘要
 DESCRIPTION (provided by applicant): An organism's genome must be accurately replicated and packaged into a new cell to faithfully propagate genetic material from one generation to the next. Aneuploidy, the state of having too many or too few chromosomes, is a leading cause of developmental defects (e.g. Down's syndrome), miscarriages, and failed pregnancies using assisted reproductive technology; therefore, reproductive success is completely dependent on accurate chromosome segregation. During meiosis, accurate chromosome segregation is ensured by using recombination to create COs (COs) between homologous chromosomes. Recombination is initiated by a DNA double- stranded break (DSB) that can be repaired either as a CO or a noncrossover (NCO) through a series of structural intermediates. The bifurcation in repair pathways is thought to occur early, likely at or before the time DSBs are formed, and the choice in repair outcome is a critical regulatory point in establishing the distribution of crossovers across the genome. The current proposal seeks to understand how repair outcome is decided and its role in determining the recombination landscape through three different approaches. First, the signatures of different types of recombination events (heteroduplex DNA) will be mapped across an entire metazoan genome using a genetic trick that allows the sequencing of only the maternal haploid genome. Secondly, a CRISPR-Cas9 based whole genome DSB repair assay is described that will allow repair outcome to be easily monitored and manipulated. And lastly, the roles of several factors in deciding and communicating repair outcome will be tested, including chromosome environment (location, heterochromatin, chromatin marks and chromosome compaction), the distance between DSBs, and recombination surveillance mechanisms. Each of these three approaches requires quantitative and computational skill sets that need to be developed by the candidate during the mentored phase in order for success as an independent scientist. A series of training activities is proposed included courses in computational biology and statistics, seminar attendance in the Curriculum for Bioinformatics and Computational Biology, individual training with the co-mentor, an expert mentoring panel, and immersion in the Computational Biology research groups at the sponsoring institution.
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Chromosome structural variants in meiosis
  • 批准号:
    10026482
  • 项目类别:
  • 资助金额:
    $40.24万
  • 财政年份:
    2020
  • 负责人:
    Kimberly Nicole Crown
  • 依托单位:
Chromosome structural variants in meiosis
  • 批准号:
    10472512
  • 项目类别:
  • 资助金额:
    $40.24万
  • 财政年份:
    2020
  • 负责人:
    Kimberly Nicole Crown
  • 依托单位:
Chromosome structural variants in meiosis
  • 批准号:
    10653093
  • 项目类别:
  • 资助金额:
    $40.24万
  • 财政年份:
    2020
  • 负责人:
    Kimberly Nicole Crown
  • 依托单位:
Chromosome structural variants in meiosis
  • 批准号:
    10226927
  • 项目类别:
  • 资助金额:
    $40.24万
  • 财政年份:
    2020
  • 负责人:
    Kimberly Nicole Crown
  • 依托单位:
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