Investigating the function of a ClpC/Hsp100-type chaperone in chloroplast preprotein import
研究 ClpC/Hsp100 型伴侣在叶绿体前蛋白输入中的功能
基本信息
- 批准号:BB/J017256/2
- 负责人:
- 金额:$ 33.87万
- 依托单位:
- 依托单位国家:英国
- 项目类别:Research Grant
- 财政年份:2013
- 资助国家:英国
- 起止时间:2013 至 无数据
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Chloroplasts and mitochondria are normal components of many cells - they are sub-cellular structures called organelles. Interestingly, these two organelles evolved from bacteria that were engulfed by other cells more than a billion years ago, and in many ways they still resemble free-living bacteria. Chloroplasts are found in plant cells, contain the green pigment chlorophyll, and are exclusively responsible for the reactions of photosynthesis (the process that captures sunlight energy and uses it to power the activities of the cell). Since photosynthesis is the only significant mechanism of energy-input into the living world, chloroplasts are of inestimable importance, not just to plants but to all life on Earth. Chloroplasts are also important in many other ways, since they play essential roles in the biosynthesis of oils, proteins and starch. Although chloroplasts do contain DNA (which is a relic from their ancient, evolutionary past as free-living photosynthetic bacteria), and are therefore able to make some of their own proteins, over 90% of the 3000 or so proteins required to build a fully functional chloroplast are encoded on DNA within the cell nucleus. The majority of chloroplast proteins are therefore made outside of the chloroplast, in the cellular matrix known as the cytosol. Since chloroplasts are each surrounded by a double membrane, or envelope, that is impervious to the passive movement of proteins, this presents a significant problem. To overcome the problem, chloroplasts have evolved a sophisticated protein import apparatus, which uses energy (in the form of ATP) to drive the import of proteins from the cytosol, across the envelope, and into the chloroplast interior. This protein import apparatus comprises two molecular machines: one in the outer envelope membrane called TOC (an abbreviation of "Translocon at the outer envelope membrane of chloroplasts"), and another in the inner envelope membrane called TIC. This project is focused on the TIC machine, and in particular on a protein called Hsp93 which is associated with the TIC complex. This Hsp93 protein is an ATPase (i.e. it hydrolyses ATP to release energy), and is a member of a family of proteins called the "molecular chaperones". Such chaperone proteins are able to bind to other proteins, particularly when they are in an unfolded state. In doing this, some chaperones can exert a "pulling force" on the target protein, to facilitate its passage from one location to another. Based on several lines of evidence, Hsp93 is thought to provide the driving force for chloroplast protein import, and to act by pulling on those proteins that need to be imported (i.e. it is believed to be a core part of the so-called "chloroplast protein import motor"). Thus, much of the ATP consumption that occurs during the import mechanism is tentatively attributed to Hsp93. However, direct proof of these hypotheses is still lacking. We propose to test these ideas directly, by manipulating the activities of the Hsp93 protein in intact plants, and assessing the consequences of such manipulations on chloroplast protein import efficiency. Because chloroplasts carry out essential functions, and because protein import is essential for chloroplast development, it should come as no surprise to learn that plants without a functional chloroplast protein import machinery are unable to survive (in fact, they die at the embryo stage). Thus, chloroplast protein import is an essential process for plants. Similarly, since we are all ultimately dependent upon plant products for survival, it follows that chloroplast protein import is essential on a global scale. What is more, since chloroplasts play a major role in the synthesis of many economically important products (such as oils and starch), a more complete understanding of how these organelles develop may enable us to enhance the productivity of crop plants, or otherwise manipulate their products.
叶绿体和线粒体是许多细胞的正常组成部分 - 它们是称为细胞器的亚细胞结构。有趣的是,这两种细胞器是从十亿多年前被其他细胞吞噬的细菌进化而来的,并且在许多方面它们仍然类似于自由生活的细菌。叶绿体存在于植物细胞中,含有绿色色素叶绿素,专门负责光合作用反应(捕获阳光能量并利用其为细胞活动提供动力的过程)。由于光合作用是向生命世界输入能量的唯一重要机制,因此叶绿体不仅对植物而且对地球上的所有生命都具有不可估量的重要性。叶绿体在许多其他方面也很重要,因为它们在油、蛋白质和淀粉的生物合成中发挥着重要作用。尽管叶绿体确实含有 DNA(这是它们作为自由生活的光合细菌的古老进化过程中的遗物),因此能够制造一些自己的蛋白质,但在构建完整的叶绿体所需的 3000 种左右蛋白质中,90% 以上是叶绿体中的 DNA。功能性叶绿体由细胞核内的 DNA 编码。因此,大多数叶绿体蛋白是在叶绿体外部、称为胞质溶胶的细胞基质中产生的。由于叶绿体均被双层膜或包膜包围,而蛋白质的被动运动不受其影响,因此这提出了一个重大问题。为了克服这个问题,叶绿体进化出了一种复杂的蛋白质输入装置,它使用能量(以 ATP 的形式)驱动蛋白质从细胞质输入,穿过包膜,进入叶绿体内部。这种蛋白质输入装置由两个分子机器组成:一个位于外膜,称为 TOC(“叶绿体外膜转运蛋白”的缩写),另一个位于内膜,称为 TIC。该项目的重点是 TIC 机器,特别是与 TIC 复合物相关的一种名为 Hsp93 的蛋白质。这种 Hsp93 蛋白是一种 ATP 酶(即它水解 ATP 以释放能量),并且是称为“分子伴侣”的蛋白质家族的成员。这种伴侣蛋白能够与其他蛋白结合,特别是当它们处于未折叠状态时。在此过程中,一些伴侣可以对目标蛋白施加“拉力”,以促进其从一个位置到另一个位置的传递。基于多项证据,Hsp93被认为为叶绿体蛋白质输入提供驱动力,并通过拉动那些需要输入的蛋白质来发挥作用(即,它被认为是所谓的“叶绿体蛋白质的核心部分”)蛋白质输入马达”)。因此,导入机制期间发生的大部分 ATP 消耗暂时归因于 Hsp93。然而,这些假设仍然缺乏直接证据。我们建议通过操纵完整植物中 Hsp93 蛋白的活性来直接测试这些想法,并评估此类操作对叶绿体蛋白输入效率的影响。由于叶绿体执行基本功能,并且蛋白质输入对于叶绿体发育至关重要,因此,没有功能性叶绿体蛋白质输入机制的植物无法生存(事实上,它们在胚胎阶段就死亡)也就不足为奇了。因此,叶绿体蛋白的输入是植物的一个重要过程。同样,由于我们最终都依赖植物产品生存,因此叶绿体蛋白的进口在全球范围内至关重要。更重要的是,由于叶绿体在许多重要经济产品(例如油和淀粉)的合成中发挥着重要作用,因此更全面地了解这些细胞器的发育方式可能使我们能够提高农作物的生产力,或以其他方式操纵它们产品。
项目成果
期刊论文数量(7)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Evolutionary, molecular and genetic analyses of Tic22 homologues in Arabidopsis thaliana chloroplasts.
拟南芥叶绿体中 Tic22 同源物的进化、分子和遗传分析。
- DOI:http://dx.10.1371/journal.pone.0063863
- 发表时间:2013
- 期刊:
- 影响因子:3.7
- 作者:Kasmati AR
- 通讯作者:Kasmati AR
Genetic and Physical Interaction Studies Reveal Functional Similarities between ALBINO3 and ALBINO4 in Arabidopsis.
遗传和物理相互作用研究揭示了拟南芥中 ALBINO3 和 ALBINO4 之间的功能相似性。
- DOI:http://dx.10.1104/pp.15.00376
- 发表时间:2015
- 期刊:
- 影响因子:7.4
- 作者:Trösch R
- 通讯作者:Trösch R
Suppressors of the Chloroplast Protein Import Mutant tic40 Reveal a Genetic Link between Protein Import and Thylakoid Biogenesis.
叶绿体蛋白输入突变体 tic40 的抑制剂揭示了蛋白输入和类囊体生物发生之间的遗传联系。
- DOI:http://dx.10.1105/tpc.16.00962
- 发表时间:2017
- 期刊:
- 影响因子:0
- 作者:Bédard J
- 通讯作者:Bédard J
Biogenesis and homeostasis of chloroplasts and other plastids.
叶绿体和其他质体的生物发生和稳态。
- DOI:http://dx.10.1038/nrm3702
- 发表时间:2013
- 期刊:
- 影响因子:0
- 作者:Jarvis P
- 通讯作者:Jarvis P
Molecular chaperone involvement in chloroplast protein import.
分子伴侣参与叶绿体蛋白输入。
- DOI:http://dx.10.1016/j.bbamcr.2012.03.019
- 发表时间:2013
- 期刊:
- 影响因子:0
- 作者:Flores
- 通讯作者:Flores
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Paul Jarvis其他文献
The Association Between Interlimb Asymmetry and Athletic Performance Tasks: A Season-Long Study in Elite Academy Soccer Players
肢间不对称性与运动表现任务之间的关联:针对精英学院足球运动员的长达一个赛季的研究
- DOI:
10.1519/jsc.0000000000003526 - 发表时间:
2020-02-27 - 期刊:
- 影响因子:3.2
- 作者:
C. Bishop;P. Read;Tom Bromley;J. Brazier;Paul Jarvis;Shyam Chavda;A. Turner - 通讯作者:
A. Turner
葉緑体オートファジー誘導に関わる葉緑体包膜修飾因子の探索:ユビキチンリガーゼの関与について
寻找参与叶绿体自噬诱导的叶绿体包膜修饰剂:泛素连接酶的参与
- DOI:
- 发表时间:
2017 - 期刊:
- 影响因子:0
- 作者:
菊池悠太;中村咲耶;Qihua Ling;Paul Jarvis;日出間純;泉正範 - 通讯作者:
泉正範
Supporting Creativity and Appreciation of Uncertainty in Exploring Geo-coded Public Health Data
支持探索地理编码公共卫生数据时的创造力和对不确定性的认识
- DOI:
- 发表时间:
2009 - 期刊:
- 影响因子:1.7
- 作者:
S. Thew;Alistair Sutcliffe;O. Bruijn;John McNaught;Rob Procter;Paul Jarvis;Iain Buchan - 通讯作者:
Iain Buchan
Student nurses perceptions of spirituality and competence in delivering spiritual care: a European pilot study.
学生护士对灵性和提供精神护理能力的看法:一项欧洲试点研究。
- DOI:
10.1016/j.nedt.2013.09.014 - 发表时间:
2014-05-01 - 期刊:
- 影响因子:3.9
- 作者:
L. Ross;R. van Leeuwen;Donia R. Baldacchino;T. Giske;W. Mcsherry;Dr Aru Narayanasamy;C. Downes;Paul Jarvis;Annemiek Schep - 通讯作者:
Annemiek Schep
Intracellular signalling: The chloroplast talks!
细胞内信号传导:叶绿体会说话!
- DOI:
10.1016/s0960-9822(01)00171-3 - 发表时间:
2001-04-17 - 期刊:
- 影响因子:9.2
- 作者:
Paul Jarvis - 通讯作者:
Paul Jarvis
Paul Jarvis的其他文献
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{{ truncateString('Paul Jarvis', 18)}}的其他基金
Defining the role of SUMO in regulating chloroplast biogenesis and functions
定义 SUMO 在调节叶绿体生物发生和功能中的作用
- 批准号:
BB/W015021/1 - 财政年份:2023
- 资助金额:
$ 33.87万 - 项目类别:
Research Grant
Uncovering how plant pathogens take control of chloroplast protein import to limit chloroplast-mediated immunity
揭示植物病原体如何控制叶绿体蛋白输入以限制叶绿体介导的免疫
- 批准号:
BB/X000192/1 - 财政年份:2023
- 资助金额:
$ 33.87万 - 项目类别:
Research Grant
Defining the scope and components of ubiquitin-dependent chloroplast-associated protein degradation
定义泛素依赖性叶绿体相关蛋白降解的范围和组成部分
- 批准号:
BB/V007300/1 - 财政年份:2021
- 资助金额:
$ 33.87万 - 项目类别:
Research Grant
Application of the plastidic E3 ligase SP1 in crop improvement, using tomato and rice as models
质体E3连接酶SP1在作物改良中的应用(以番茄和水稻为模型)
- 批准号:
BB/R005591/1 - 财政年份:2018
- 资助金额:
$ 33.87万 - 项目类别:
Research Grant
Elucidating the role of SP2 and the SP1-SP2 machinery in chloroplast protein degradation
阐明 SP2 和 SP1-SP2 机制在叶绿体蛋白质降解中的作用
- 批准号:
BB/R016984/1 - 财政年份:2018
- 资助金额:
$ 33.87万 - 项目类别:
Research Grant
Chloroplast-Associated Degradation (CHLORAD): Molecular definition of a ubiquitin-dependent system for plastid protein removal in plants
叶绿体相关降解 (CHLORAD):植物中质体蛋白去除泛素依赖性系统的分子定义
- 批准号:
BB/R009333/1 - 财政年份:2018
- 资助金额:
$ 33.87万 - 项目类别:
Research Grant
Role of the chloroplast ubiquitin E3 ligase SP1 in abiotic stress tolerance in plants
叶绿体泛素 E3 连接酶 SP1 在植物非生物胁迫耐受中的作用
- 批准号:
BB/N006372/1 - 财政年份:2016
- 资助金额:
$ 33.87万 - 项目类别:
Research Grant
Control of plastid biogenesis by the ubiquitin-proteasome system
泛素-蛋白酶体系统对质体生物发生的控制
- 批准号:
BB/K018442/1 - 财政年份:2013
- 资助金额:
$ 33.87万 - 项目类别:
Research Grant
Investigating the roles of Arabidopsis STIC1 and STIC2 in chloroplast protein transport
研究拟南芥 STIC1 和 STIC2 在叶绿体蛋白转运中的作用
- 批准号:
BB/J009369/2 - 财政年份:2013
- 资助金额:
$ 33.87万 - 项目类别:
Research Grant
Investigating the roles of Arabidopsis STIC1 and STIC2 in chloroplast protein transport
研究拟南芥 STIC1 和 STIC2 在叶绿体蛋白转运中的作用
- 批准号:
BB/J009369/1 - 财政年份:2012
- 资助金额:
$ 33.87万 - 项目类别:
Research Grant
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