Characterization of a new class of nuclear localization signals
Characterization of a new class of nuclear localization signals
批准号:
RGPIN-2019-05222
负责人:
Kapus, Andras
金额:
$4.23万
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
项目状态:
已结题
起止时间:
2022-01-01 至 2023-12-31
中文摘要
动物和人类细胞的细胞核是一个至关重要的细胞器,它包含了我们所有的基因和调节它们的机制。控制基因表达,即从我们的基因蓝图DNA到构建我们蛋白质的分子“装配线”的信息的调节转移,对于所有细胞功能,包括生长、增殖、代谢和运动,都是必不可少的。细胞核和细胞其他部分之间的信息传递需要蛋白质连续而微妙地进出细胞核。近似的。人体两万种不同的蛋白质,几乎三分之一(约6000种)有能力定位到细胞核。核的进出,也称为核的进出口,是通过核孔(NP)这一特殊的通道进行的。这种大的蛋白质复合物既是向导又是屏障,从而控制蛋白质在核膜上的穿梭。了解这种对所有正常细胞功能至关重要的交通,是细胞生物学的一个基本重要方面。NP如何识别哪些分子要运输(即哪些是“货物”)以及它们应该往哪个方向(进口或出口)?货物分子包含“分子邮政编码”或所谓的核定位和核出口信号(NLS和NES)。这些分子片段与运输机械的元件相互作用。然而,令人惊讶的是,这些邮政编码在60%的穿梭蛋白中是未知的。在我们之前关于生长促进蛋白调控的工作中,我们发现了一个新的序列,它具有介导核输入的能力。这是一个独特的邮政编码,与所有已知的国家邮政编码大不相同。我们还发现,这种新信号的输入是由机械因素调节的,通过细胞骨架起作用。重要的是,我们还在一整套其他不相关的蛋白质中发现了类似的分子特征(序列的变体),这些蛋白质都是已知控制基因表达的。这些蛋白在脂质代谢、细胞生长和免疫防御等多种功能中发挥关键作用。然而,我们不知道这些发现序列的变异是否会带来输入和影响蛋白质的功能。根据我们的研究结果,我们假设这个分子特征代表了一类新的NLS。我们研究项目的目的是表征这种NLS。我们希望确定其有效进入核所需的关键特征,其进口的机制和调节以及它在包含它的蛋白质的定位和功能中的作用。我们已经开始建立一个全新的分子工具包,这将使我们能够监测核交通和新的NLS的功能。因此,这些研究有能力揭示一类全新的核定位信号,这是理解核传输的重要一步,核传输是所有重要功能的基本过程。
英文摘要
The nucleus of animal and human cells is a vitally important cellular organelle that contains all our genes and the machinery that regulates them. Controlled gene expression, i.e. the regulated transfer of information from our genetic blueprint, the DNA, to the molecular "assembly lines" that build up our proteins is indispensable for all cellular function, including, growth, proliferation, metabolism and movement. Information transfer between the nucleus and other parts of the cells requires the continuous and subtly controlled entry and exit of proteins into and out of the nucleus. Of the approx. 20,000 different proteins of the human body, almost one third (>6000) has the capacity to localize to the nucleus. Entry and exit - also called nuclear import and export - occurs via specialized gates, the nuclear pore (NP). This large protein complex acts both as a guide and a barrier, thereby controlling the shuttling of proteins across the nuclear membrane. Understanding this traffic, which is essential for all normal cell functions, is a fundamentally important aspect of cell biology. How does the NP recognize which molecules are to be transported (i.e. which is the "cargo") and which direction they should go (import or export)? Cargo molecules contain "molecular postal codes" or so called nuclear localization and nuclear export signals (NLS and NES). These molecular segments interact with elements of the transport machinery. Surprisingly, however, such postal codes are unknown in 60% of shuttling proteins. During our previous work on the regulation of a growth-promoting protein, we identified a new sequence, which has the capacity to mediate nuclear import. This is a unique postal code, which vastly differs from all the known NLS. We also discovered that import of this new signal is regulated by mechanical factors, acting via the cell's skeleton. Importantly, we also found similar molecular signatures (variant of the sequence) in a whole set of other, unrelated proteins, which are all known to control gene expression. These proteins play key role in variety of functions, including lipid metabolism, cell growth and immune defense. However we do not know if these variants of the discovered sequence can bring about import and affect protein function. Based on our results, we hypothesize that this molecular signature represents a new class of NLS. The objective of our research program is to characterize this NLS. We wish to identify the critical features necessary for its efficient nuclear entry, the mechanism and regulation of its import and its role in the localization and function of the proteins that contain it. We have started building a whole new molecular toolkit, which will allow us to monitor the nuclear traffic and function of the new NLS. These studies therefore have the capacity to unravel an entirely new class of nuclear localization signals, major step in understanding nuclear traffic, a fundamental process in all vital functions.
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Characterization of a new class of nuclear localization signals
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批准号:RGPIN-2019-05222
-
项目类别:Discovery Grants Program - Individual
-
资助金额:$4.23万
-
财政年份:2021
-
负责人:Kapus, Andras
-
依托单位:
Characterization of a new class of nuclear localization signals
-
批准号:RGPIN-2019-05222
-
项目类别:Discovery Grants Program - Individual
-
资助金额:$4.23万
-
财政年份:2020
-
负责人:Kapus, Andras
-
依托单位:
Characterization of a new class of nuclear localization signals
-
批准号:RGPIN-2019-05222
-
项目类别:Discovery Grants Program - Individual
-
资助金额:$4.23万
-
财政年份:2019
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负责人:Kapus, Andras
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依托单位:
Cytoskeleton-mitochondrion interactions during cellular stress
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批准号:227908-2013
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项目类别:Discovery Grants Program - Individual
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资助金额:$2.62万
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财政年份:2017
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负责人:Kapus, Andras
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依托单位:
Cytoskeleton-mitochondrion interactions during cellular stress
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批准号:227908-2013
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项目类别:Discovery Grants Program - Individual
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资助金额:$2.62万
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财政年份:2015
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依托单位:
Cytoskeleton-mitochondrion interactions during cellular stress
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批准号:227908-2013
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项目类别:Discovery Grants Program - Individual
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资助金额:$2.62万
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财政年份:2014
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负责人:Kapus, Andras
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依托单位:
Cytoskeleton-mitochondrion interactions during cellular stress
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批准号:227908-2013
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项目类别:Discovery Grants Program - Individual
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资助金额:$2.62万
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Long-term live fluorescent imaging system for monitoring site-specific functions in epithelia
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批准号:458801-2014
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Expression, localization and function of epithelial ion transporters under physiological and pathological conditions
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批准号:227908-2005
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项目类别:Discovery Grants Program - Individual
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资助金额:$2.4万
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财政年份:2010
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Expression, localization and function of epithelial ion transporters under physiological and pathological conditions
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批准号:227908-2005
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依托单位:
Expression, localization and function of epithelial ion transporters under physiological and pathological conditions
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批准号:227908-2005
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资助金额:$2.4万
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依托单位:
Expression, localization and function of epithelial ion transporters under physiological and pathological conditions
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批准号:227908-2005
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项目类别:Discovery Grants Program - Individual
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资助金额:$2.4万
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财政年份:2006
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负责人:Kapus, Andras
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依托单位:
Expression, localization and function of epithelial ion transporters under physiological and pathological conditions
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批准号:227908-2005
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项目类别:Discovery Grants Program - Individual
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资助金额:$2.4万
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财政年份:2005
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负责人:Kapus, Andras
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Osmotic regulation of the Na+-K+2Cl- cotransporter
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批准号:227908-2004
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项目类别:Discovery Grants Program - Individual
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负责人:Kapus, Andras
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依托单位:
Volume-dependent reorganization of the cytoskeleton
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批准号:227908-2000
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项目类别:Discovery Grants Program - Individual
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负责人:Kapus, Andras
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依托单位:
Volume-dependent reorganization of the cytoskeleton
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批准号:227908-2000
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项目类别:Discovery Grants Program - Individual
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资助金额:$2.19万
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依托单位:
Volume-dependent reorganization of the cytoskeleton
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批准号:227908-2000
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项目类别:Discovery Grants Program - Individual
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资助金额:$2.19万
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财政年份:2001
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依托单位:
Volume-dependent reorganization of the cytoskeleton
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批准号:227908-2000
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项目类别:Discovery Grants Program - Individual
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资助金额:$2.19万
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财政年份:2000
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负责人:Kapus, Andras
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