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Mapping epistasis in molecular evolution: the influenza nucleoprotein

Mapping epistasis in molecular evolution: the influenza nucleoprotein
绘制分子进化中的上位性:流感核蛋白
批准号:
9067390
负责人:
Jesse D Bloom
金额:
$32.59万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-01 至 2018-05-31

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中文摘要
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DESCRIPTION (provided by applicant): Epistasis occurs when the effect of one allele is influenced by another allele. Epistatic interactions play a profound role in evolution. An understanding of epistasis is also crucial in a variety of biomedical endeavors, such as identifying disease variants from genetic association studies and predicting the evolution of pathogens. But many of the most basic questions about epistasis remain unanswered, including: How common are epistatic interactions? How do they arise? And what are the underlying molecular mechanisms? We will address these questions by mapping epistatic interactions along a real evolutionary trajectory. To do this, we will employ a combination of computational and experimental tools to study the influenza nucleoprotein. Because of the unique nature of influenza evolution, we are able to infer in step-by-step detail the 39 mutations that have occurred in the nucleoprotein from human H3N2 since the year 1968. We will construct all 39 intermediate proteins along this evolutionary trajectory. We will also introduce each of the mutations individually into the 1968 parent. All of these variants will be tested for biochemical function and effect on viral fitness. This will provide a clear experimental test for epistasis: a mutation is involved in an epistatic interaction if it has a different effect in the 1968 parent than in the evolutionary intermediate in which it actually occurred. Crucially, our preliminary work has already identified several mutations involved in epistatic interactions. In Aim 1, we will build on this work by mapping all epistatic interactions since 1968. In Aim 2, we will address the mystery of how the epistatic interactions arose - did multiple mutations occur simultaneously, were there compensatory or permissive mutations, or did epistasis arise slowly due to a gradually shifting genetic background? Finally, in Aim 3, we will use biophysical and biochemical techniques to identify the molecular mechanisms of each epistatic interaction. At the conclusion of this study, we will have mapped the prevalence, origins, and mechanisms of epistatic interactions along a real evolutionary trajectory. Our findings will provide a new window into one of the most important factors shaping the evolution of proteins and viruses, and will aid in attempts to interpret sequence data and understand interactions between alleles.
期刊论文(13)
专著(0)
科研奖励(0)
会议论文
Cooperating H3N2 Influenza Virus Variants Are Not Detectable in Primary Clinical Samples.
在主要临床样本中无法检测到 H3N2 流感病毒协同变异体。
DOI: 10.1128/mspheredirect.00552-17
发表时间: 2018
期刊: mSphere
影响因子: 4.8
作者: [Xue,KatherineS, Greninger,AlexanderL, Pérez-Osorio,Ailyn, Bloom,JesseD]
通讯作者: Bloom,JesseD
DOI: 10.7554/elife.13974
发表时间: 2016-03-15
期刊: eLife
影响因子: 7.7
作者: [Xue KS, Hooper KA, Ollodart AR, Dingens AS, Bloom JD]
通讯作者: Bloom JD
DOI: 10.1186/s13062-016-0172-z
发表时间: 2017-01-17
期刊: Biology direct
影响因子: 5.5
作者: [Bloom JD]
通讯作者: Bloom JD
DOI: 10.7554/elife.03300
发表时间: 2014-07-08
期刊: eLife
影响因子: 7.7
作者: [Thyagarajan B, Bloom JD]
通讯作者: Bloom JD
7
    Core C: Viral Evolution
    • 批准号:
      10425028
    • 项目类别:
    • 资助金额:
      $122.53万
    • 财政年份:
      2022
    • 负责人:
      Jesse D Bloom
    • 依托单位:
    Prospectively characterizing the functional and antigenic effects of mutations to viral entry proteins
    • 批准号:
      10593369
    • 项目类别:
    • 资助金额:
      $34.36万
    • 财政年份:
      2018
    • 负责人:
      Jesse D Bloom
    • 依托单位:
    Prospectively characterizing the functional and antigenic effects of mutations to viral entry proteins
    Complete mapping of immune selection from antibodies to HIV
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