Uncovering the Molecular Mechanisms of Selfish Genetic Elements

揭示自私遗传元件的分子机制

基本信息

  • 批准号:
    1244772
  • 负责人:
  • 金额:
    $ 64.51万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
    Continuing Grant
  • 财政年份:
    2013
  • 资助国家:
    美国
  • 起止时间:
    2013-03-01 至 2018-02-28
  • 项目状态:
    已结题

项目摘要

Intellectual Merit: Advantageous genes normally persist and predominate in populations, while deleterious genes disappear. However, some non-adaptive genes have found ways to counter the forces of natural selection and infiltrate populations; these are known as selfish genetic elements or selfish genes. Such elements are able to increase in frequency and spread through populations by employing genetic mechanisms that circumvent Mendel's laws of inheritance. A fascinating case is that of the Maternal-Effect Dominant Embryonic Arrest (Medea) elements in the red flour beetle, Tribolium castaneum. Heterozygous Medea females transmit a dominant-lethal factor to hatchlings, but the lethal effect is shut down in those progeny that inherit a Medea allele from either parent. Thus, each Medea allele encodes both a maternally loaded "poison" and an "antidote" expressed in the embryo. Little is known about how such elements function. Therefore, this project is aimed at discovering the molecular mechanism responsible for Medea's selfish behavior by using genetic and genomic tools to uncover the genes involved in self-selection. Broader Impacts: This project will increase our understanding of how selfish genes escape natural selection and infiltrate populations. This knowledge could provide a new mechanism for transferring traits into pest populations to make them less problematic. The project includes several educational components. The PI is participating in an NSF Integrative Graduate Education and Research Traineeship (Genetic Engineering and Society: The case of transgenic pests) that is focused on training students in technologies used for manipulation of pest genomes as well as methods needed to assess the environmental and sociocultural appropriateness of specific products of these genetic manipulations. This research will be integrated directly into IGERT courses and research of IGERT graduate fellows. The project also includes activities that will provide undergraduates from underrepresented groups with an opportunity to participate in cutting-edge functional genomic research. Moreover, this research will be widely disseminated through outreach events by the PI and IGERT students to raise public awareness about the utility of transgenic technologies.
智力优点:有害基因通常在种群中持续存在并占主导地位,而有害基因则消失。然而,一些非适应性基因已经找到了对抗自然选择的力量并渗透到种群中的方法;这些被称为自私遗传因素或自私基因。这些因素能够增加频率,并通过采用遗传机制,绕过孟德尔的遗传规律在人群中传播。一个有趣的案例是红粉甲虫赤拟谷盗(Tribolium castaneum)中的母体效应显性胚胎停滞(美狄亚)元素。杂合的美狄亚雌性将显性致死因子传递给孵化的幼仔,但在从父母任何一方继承美狄亚等位基因的后代中,这种致死效应被关闭。因此,每一个美狄亚等位基因都编码了母体携带的“毒药”和胚胎中表达的“解毒剂”。人们对这些元素的功能知之甚少。因此,该项目旨在通过使用遗传和基因组工具来揭示参与自我选择的基因,从而发现美狄亚自私行为的分子机制。 更广泛的影响:这个项目将增加我们对自私基因如何逃避自然选择和渗透种群的理解。这种知识可以提供一种新的机制,将性状转移到害虫种群中,使它们的问题减少。该项目包括几个教育部分。主要研究员正在参加国家科学基金会的综合研究生教育和研究培训(遗传工程与社会:转基因害虫的案例),该培训的重点是培训学生掌握用于操纵害虫基因组的技术以及评估这些遗传操纵的特定产品的环境和社会文化适当性所需的方法。这项研究将直接纳入IGERT课程和IGERT研究生研究员的研究。该项目还包括一些活动,将为来自代表性不足群体的本科生提供参与尖端功能基因组研究的机会。此外,这项研究将通过PI和IGERT学生的外联活动广泛传播,以提高公众对转基因技术实用性的认识。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

Marce Lorenzen其他文献

Marce Lorenzen的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

相似国自然基金

Kidney injury molecular(KIM-1)介导肾小管上皮细胞自噬在糖尿病肾病肾间质纤维化中的作用
  • 批准号:
    81300605
  • 批准年份:
    2013
  • 资助金额:
    23.0 万元
  • 项目类别:
    青年科学基金项目
Molecular Plant
  • 批准号:
    31224801
  • 批准年份:
    2012
  • 资助金额:
    20.0 万元
  • 项目类别:
    专项基金项目
Molecular Interaction Reconstruction of Rheumatoid Arthritis Therapies Using Clinical Data
  • 批准号:
    31070748
  • 批准年份:
    2010
  • 资助金额:
    34.0 万元
  • 项目类别:
    面上项目
Molecular Plant
  • 批准号:
    31024802
  • 批准年份:
    2010
  • 资助金额:
    20.0 万元
  • 项目类别:
    专项基金项目
Cellular & Molecular Immunology
  • 批准号:
    30824806
  • 批准年份:
    2008
  • 资助金额:
    20.0 万元
  • 项目类别:
    专项基金项目

相似海外基金

Uncovering cargo and cell type specific molecular mechanisms of renal tubular epithelial transport
揭示肾小管上皮运输的货物和细胞类型特异性分子机制
  • 批准号:
    10705236
  • 财政年份:
    2022
  • 资助金额:
    $ 64.51万
  • 项目类别:
Uncovering circuit and molecular mechanisms of restraint of motivated behavior
揭示抑制动机行为的回路和分子机制
  • 批准号:
    473552
  • 财政年份:
    2022
  • 资助金额:
    $ 64.51万
  • 项目类别:
    Fellowship Programs
Uncovering molecular mechanisms of metastatic rhabdomyosarcoma
揭示转移性横纹肌肉瘤的分子机制
  • 批准号:
    486072
  • 财政年份:
    2022
  • 资助金额:
    $ 64.51万
  • 项目类别:
    Studentship Programs
Uncovering the cellular and molecular mechanisms of folic acid fortification in neural tube defects
揭示叶酸强化治疗神经管缺陷的细胞和分子机制
  • 批准号:
    10595548
  • 财政年份:
    2022
  • 资助金额:
    $ 64.51万
  • 项目类别:
Uncovering the Cellular and Molecular Mechanisms Driving B-cell Neogenesis During Regeneration
揭示再生过程中驱动 B 细胞新生的细胞和分子机制
  • 批准号:
    10315184
  • 财政年份:
    2021
  • 资助金额:
    $ 64.51万
  • 项目类别:
NSF Postdoctoral Fellowship in Biology FY 2021: Uncovering the Molecular Mechanisms of Mitochondrial Proteostasis
2021 财年 NSF 生物学博士后奖学金:揭示线粒体蛋白质稳态的分子机制
  • 批准号:
    2109312
  • 财政年份:
    2021
  • 资助金额:
    $ 64.51万
  • 项目类别:
    Fellowship Award
NSF Postdoctoral Fellowship in Biology FY 2021: Uncovering the molecular mechanisms that govern cnidarian-algal symbiosis using forward genetic screens
2021 财年 NSF 生物学博士后奖学金:利用正向遗传筛选揭示控制刺胞动物-藻类共生的分子机制
  • 批准号:
    2109503
  • 财政年份:
    2021
  • 资助金额:
    $ 64.51万
  • 项目类别:
    Fellowship Award
Uncovering the molecular mechanisms of potassium channel activity.
揭示钾通道活性的分子机制。
  • 批准号:
    DP210102405
  • 财政年份:
    2021
  • 资助金额:
    $ 64.51万
  • 项目类别:
    Discovery Projects
Uncovering the Cellular and Molecular Mechanisms Driving B-cell Neogenesis During Regeneration
揭示再生过程中驱动 B 细胞新生的细胞和分子机制
  • 批准号:
    10455473
  • 财政年份:
    2021
  • 资助金额:
    $ 64.51万
  • 项目类别:
Uncovering Molecular Mechanisms Underlying Cell-to-Cell Movement and Long-Distance Trafficking of Viruses in Plants
揭示植物细胞间运动和病毒远距离贩运的分子机制
  • 批准号:
    RGPIN-2015-05117
  • 财政年份:
    2019
  • 资助金额:
    $ 64.51万
  • 项目类别:
    Discovery Grants Program - Individual
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了