Determining spatial arrangement, stoichiometry, and substrate specificity of messenger RNA-binding proteins along the gene expression pathway.

确定基因表达途径中信使 RNA 结合蛋白的空间排列、化学计量和底物特异性。

基本信息

  • 批准号:
    RGPIN-2020-06924
  • 负责人:
  • 金额:
    $ 3.06万
  • 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:
    2022
  • 资助国家:
    加拿大
  • 起止时间:
    2022-01-01 至 2023-12-31
  • 项目状态:
    已结题

项目摘要

The long-term objective of our research program is to study the maturation pathways of essential RNA-protein complexes in different organisms. The expression of our genes is tightly regulated both during the reading and copying of our DNA into messenger RNA (mRNA), the encoding template, and during translation, when the information in this template is converted into proteins. However, transcription and translation are not the only steps where regulation and alteration of our genetic material can occur. mRNA itself is bound by many proteins that further process, fold and inspect the molecule to ensure its correctness and hence the correct transmission of genetic code into proteins for diverse processes in the cell. While it has been assumed that all mRNA molecules are uniformly processed, or matured, by the same set of proteins, recent data from our lab suggests that there may be variation in these maturation steps that are defined by the variance in proteins associating with different mRNAs during these steps. This project proposes to further explore these suggested variances in mRNA maturation, by investigating the mRNAs involved, the underlying mechanisms that lead to variances, and their consequences, as any misstep in this process could lead to the introduction of errors resulting in disease. Overall, a more detailed basic knowledge of any additional regulatory steps during the expression of our genetic material will provide us with better fundamental understanding of gene regulation as well as why certain diseases may develop and potential new entry points for treatment in the future.
我们研究计划的长期目标是研究不同生物体中必需RNA-蛋白质复合物的成熟途径。我们基因的表达在阅读DNA并将其复制为信使RNA(mRNA)(编码模板)的过程中,以及在翻译过程中(模板中的信息转化为蛋白质)受到严格的调控。然而,转录和翻译并不是调节和改变我们遗传物质的唯一步骤。mRNA本身被许多蛋白质结合,这些蛋白质进一步加工、折叠和检查分子以确保其正确性,从而将遗传密码正确地传递到蛋白质中以用于细胞中的不同过程。虽然已经假设所有mRNA分子都是由同一组蛋白质统一加工或成熟的,但我们实验室的最新数据表明,这些成熟步骤中可能存在变化,这些变化是由这些步骤中与不同mRNA相关的蛋白质的差异所定义的。该项目建议通过调查所涉及的mRNA,导致差异的潜在机制及其后果来进一步探索这些mRNA成熟的差异,因为这个过程中的任何失误都可能导致引入导致疾病的错误。总的来说,对我们遗传物质表达过程中任何额外调控步骤的更详细的基本知识将为我们提供对基因调控的更好的基本理解,以及为什么某些疾病可能发展和未来治疗的潜在新切入点。

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)

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Oeffinger, Marlene其他文献

Differential affinity purification and mass spectrometry analysis of two nuclear pore complex isoforms in yeast S. cerevisiae.
  • DOI:
    10.1016/j.xpro.2023.102359
  • 发表时间:
    2023-09-15
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Bensidoun, Pierre;Zenklusen, Daniel;Oeffinger, Marlene
  • 通讯作者:
    Oeffinger, Marlene
To the pore and through the pore: a story of mRNA export kinetics.
Nuclear mRNA metabolism drives selective basket assembly on a subset of nuclear pore complexes in budding yeast.
  • DOI:
    10.1016/j.molcel.2022.09.019
  • 发表时间:
    2022-10-20
  • 期刊:
  • 影响因子:
    16
  • 作者:
    Bensidoun, Pierre;Reiter, Taylor;Montpetit, Ben;Zenklusen, Daniel;Oeffinger, Marlene
  • 通讯作者:
    Oeffinger, Marlene
A robust pipeline for rapid production of versatile nanobody repertoires.
  • DOI:
    10.1038/nmeth.3170
  • 发表时间:
    2014-12
  • 期刊:
  • 影响因子:
    48
  • 作者:
    Fridy, Peter C.;Li, Yinyin;Keegan, Sarah;Thompson, Mary K.;Nudelman, Ilona;Scheid, Johannes F.;Oeffinger, Marlene;Nussenzweig, Michel C.;Fenyo, David;Chait, Brian T.;Rout, Michael P.
  • 通讯作者:
    Rout, Michael P.
Adaptive partitioning of a gene locus to the nuclear envelope in Saccharomyces cerevisiae is driven by polymer-polymer phase separation.
酿酒酵母中基因基因座对核神庙的自适应分配是由聚合物聚合物相分离驱动的。
  • DOI:
    10.1038/s41467-023-36391-6
  • 发表时间:
    2023-02-28
  • 期刊:
  • 影响因子:
    16.6
  • 作者:
    Gonzalez, Lidice;Kolbin, Daniel;Trahan, Christian;Jeronimo, Celia;Robert, Francois;Oeffinger, Marlene;Bloom, Kerry;Michnick, Stephen W.
  • 通讯作者:
    Michnick, Stephen W.

Oeffinger, Marlene的其他文献

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{{ truncateString('Oeffinger, Marlene', 18)}}的其他基金

Determining spatial arrangement, stoichiometry, and substrate specificity of messenger RNA-binding proteins along the gene expression pathway.
确定基因表达途径中信使 RNA 结合蛋白的空间排列、化学计量和底物特异性。
  • 批准号:
    RGPAS-2020-00019
  • 财政年份:
    2022
  • 资助金额:
    $ 3.06万
  • 项目类别:
    Discovery Grants Program - Accelerator Supplements
Determining spatial arrangement, stoichiometry, and substrate specificity of messenger RNA-binding proteins along the gene expression pathway.
确定基因表达途径中信使 RNA 结合蛋白的空间排列、化学计量和底物特异性。
  • 批准号:
    RGPAS-2020-00019
  • 财政年份:
    2021
  • 资助金额:
    $ 3.06万
  • 项目类别:
    Discovery Grants Program - Accelerator Supplements
Determining spatial arrangement, stoichiometry, and substrate specificity of messenger RNA-binding proteins along the gene expression pathway.
确定基因表达途径中信使 RNA 结合蛋白的空间排列、化学计量和底物特异性。
  • 批准号:
    RGPIN-2020-06924
  • 财政年份:
    2021
  • 资助金额:
    $ 3.06万
  • 项目类别:
    Discovery Grants Program - Individual
Determining spatial arrangement, stoichiometry, and substrate specificity of messenger RNA-binding proteins along the gene expression pathway.
确定基因表达途径中信使 RNA 结合蛋白的空间排列、化学计量和底物特异性。
  • 批准号:
    RGPIN-2020-06924
  • 财政年份:
    2020
  • 资助金额:
    $ 3.06万
  • 项目类别:
    Discovery Grants Program - Individual
Determining spatial arrangement, stoichiometry, and substrate specificity of messenger RNA-binding proteins along the gene expression pathway.
确定基因表达途径中信使 RNA 结合蛋白的空间排列、化学计量和底物特异性。
  • 批准号:
    RGPAS-2020-00019
  • 财政年份:
    2020
  • 资助金额:
    $ 3.06万
  • 项目类别:
    Discovery Grants Program - Accelerator Supplements
Determining the molecular mechanisms of ribosomal export through the nuclear pore.
确定核糖体通过核孔输出的分子机制。
  • 批准号:
    RGPIN-2015-06586
  • 财政年份:
    2019
  • 资助金额:
    $ 3.06万
  • 项目类别:
    Discovery Grants Program - Individual
Determining the molecular mechanisms of ribosomal export through the nuclear pore.
确定核糖体通过核孔输出的分子机制。
  • 批准号:
    RGPIN-2015-06586
  • 财政年份:
    2018
  • 资助金额:
    $ 3.06万
  • 项目类别:
    Discovery Grants Program - Individual
Determining the molecular mechanisms of ribosomal export through the nuclear pore.
确定核糖体通过核孔输出的分子机制。
  • 批准号:
    RGPIN-2015-06586
  • 财政年份:
    2017
  • 资助金额:
    $ 3.06万
  • 项目类别:
    Discovery Grants Program - Individual
Determining the molecular mechanisms of ribosomal export through the nuclear pore.
确定核糖体通过核孔输出的分子机制。
  • 批准号:
    RGPIN-2015-06586
  • 财政年份:
    2016
  • 资助金额:
    $ 3.06万
  • 项目类别:
    Discovery Grants Program - Individual
Determining the molecular mechanisms of ribosomal export through the nuclear pore.
确定核糖体通过核孔输出的分子机制。
  • 批准号:
    RGPIN-2015-06586
  • 财政年份:
    2015
  • 资助金额:
    $ 3.06万
  • 项目类别:
    Discovery Grants Program - Individual

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Determining spatial arrangement, stoichiometry, and substrate specificity of messenger RNA-binding proteins along the gene expression pathway.
确定基因表达途径中信使 RNA 结合蛋白的空间排列、化学计量和底物特异性。
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    RGPAS-2020-00019
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    $ 3.06万
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Determining spatial arrangement, stoichiometry, and substrate specificity of messenger RNA-binding proteins along the gene expression pathway.
确定基因表达途径中信使 RNA 结合蛋白的空间排列、化学计量和底物特异性。
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Determining spatial arrangement, stoichiometry, and substrate specificity of messenger RNA-binding proteins along the gene expression pathway.
确定基因表达途径中信使 RNA 结合蛋白的空间排列、化学计量和底物特异性。
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    $ 3.06万
  • 项目类别:
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Determining spatial arrangement, stoichiometry, and substrate specificity of messenger RNA-binding proteins along the gene expression pathway.
确定基因表达途径中信使 RNA 结合蛋白的空间排列、化学计量和底物特异性。
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    Discovery Grants Program - Individual
Determining spatial arrangement, stoichiometry, and substrate specificity of messenger RNA-binding proteins along the gene expression pathway.
确定基因表达途径中信使 RNA 结合蛋白的空间排列、化学计量和底物特异性。
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