The mitochondrial rough-ER (mt-rER), a new type of endoplasmic reticulum: from structure to function

线粒体粗面-ER(mt-rER),一种新型内质网:从结构到功能

基本信息

  • 批准号:
    RGPIN-2017-06130
  • 负责人:
  • 金额:
    $ 2.04万
  • 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:
    2019
  • 资助国家:
    加拿大
  • 起止时间:
    2019-01-01 至 2020-12-31
  • 项目状态:
    已结题

项目摘要

Inter-organellar contact sites exist between nearly all the compartments of the cell, and their study has become very topical because more and more physiological and metabolic processes are coordinated by physical interactions between organelles. One of the best characterized type of inter-organellar contact is the one that occurs between mitochondria and the smoothER, which serves to exchange calcium and regulate respiration, Ca2+ homeostasis and signalling, phospholipid biosynthesis, and more. However, mitochondria can be found associated also to the ribosome-containing roughER, but the function of this association is unknown, and whether or not this mitochondria-associated roughER (mt-rER) is a specialized type of ER remains to be determined. ******Here, we share a wealth of compelling preliminary data to propose a research program that has the objective to show that the mt-rER is a structurally distinct type of ER that controls cholesterol and fatty acids synthesis by translating and compartmentalizing the enzymes of their pathway and the lipoproteins that traffic them.******To this goal, we will capitalize on an ad-hoc developed protocol allowing the purification of mouse liver mt-rER and on our experience in cryo-electron microscopy, cryo-electron tomography, 3D imaging, transcriptomics and proteomics to show that:******1: the mt-rER is not connected to the ER network of the cell ***2: the mt-rER has a proteome that is different from that of the ER***3: the contact site between the smoothER and the mitochondrion (known as MAM or MERC) is a subdomain of the mt-rER***4: proteins of the lipids and cholesterol pathway are translated directly at the mt-rER***5: proteins of the lipids and cholesterol pathway are localized at the interface between the mt-rER and the mitochondrion***6: the mt-rER contains an active cholesterol biosynthetic pathway.******Ultimately, this research will show that the juxtaposition between the mt-rER and the mitochondrion serves to compartmentalize substrates, enzymes and precursors of the lipid and cholesterol pathway, thereby explaining how the cell can efficiently synthesize, handle and transport huge amounts of these molecules.******These discoveries will have a major impact for many. For cell biologists, because they will establish the mt-rER as a novel, structurally and functionally distinct type of ER; for cell physiologists, because they will assigning to the mt-rER a key role in putting lipids and cholesterol in circulation through the synthesis of lipoproteins; and for researchers in the MAM/MERC field because they will provide a framework for studying the mechanisms regulating the biogenesis and remodelling of this important sub-cellular compartment.**
细胞的几乎所有隔室之间都存在组织间接触位点,并且它们的研究变得非常局部,因为越来越多的生理和代谢过程通过细胞器之间的物理相互作用协调。最佳特征类型的器官间接触之一是在线粒体和平滑范围之间发生的类型,它可以交换钙并调节呼吸,Ca2+稳态和信号传导,磷脂生物合成等。但是,线粒体也可以与含核糖体更粗糙相关联,但是该关联的功能尚不清楚,并且该线粒体相关的粗糙剂(MT-RER)是否是一种专业的ER类型,仍然有待确定。 ******在这里,我们共享大量引人注目的初步数据,以提出一项研究计划,其目标表明MT率是一种在结构上不同的ER类型,它可以控制胆固醇和脂肪酸通过翻译和划分其路径的酶和将其启动的启发素来构成的固定酶来构成和划分的鼠标。 MT率以及我们在冷冻电子显微镜,冷冻电子层析成像,3D成像,转录组学和蛋白质组学方面的经验表明:****** 1:MT-RER与细胞网络无关。是MT速率*** 4:脂质和胆固醇途径的蛋白质的子域,直接在MT-RER *** 5:脂质和胆固醇途径的蛋白质上平移位于MT率和MITOCHRION的界面上,MT-RERSTIENT the MT-RERSINGITION AIRVITICTIONT the MT-RES*表明MT-RER和线粒体之间的并置可以使脂质和胆固醇途径的底物,酶和前体分裂,从而解释细胞如何有效地合成,处理和运输这些分子的大量这些发现。对于细胞生物学家而言,因为它们将在结构和功能上不同的ER类型上建立MT-RER。对于细胞生理学家而言,因为他们将通过合成脂蛋白将脂质和胆固醇分配给将脂质和胆固醇循环中的关键作用。对于MAM/MERC领域的研究人员,他们将提供一个框架,用于研究调节这一重要的亚细胞室的生物发生和重塑的机制。**

项目成果

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Pellegrini, Luca其他文献

Structural basis for inhibition of homologous recombination by the RecX protein.
  • DOI:
    10.1038/emboj.2008.145
  • 发表时间:
    2008-08-20
  • 期刊:
  • 影响因子:
    11.4
  • 作者:
    Ragone, Stefania;Maman, Joseph D.;Furnham, Nicholas;Pellegrini, Luca
  • 通讯作者:
    Pellegrini, Luca
Dual Roles of Ctf18-RFC: Loading the Clamp and Angling for the Polymerase
  • DOI:
    10.1016/j.str.2017.12.009
  • 发表时间:
    2018-01-02
  • 期刊:
  • 影响因子:
    5.7
  • 作者:
    Pellegrini, Luca
  • 通讯作者:
    Pellegrini, Luca
The dynamin GTPase OPA1: More than mitochondria?
Prevalence and correlates of current suicide risk in an international sample of OCD adults: A report from the International College of Obsessive-Compulsive Spectrum Disorders (ICOCS) network and Obsessive Compulsive and Related Disorders Network (OCRN) of the European College of Neuropsychopharmacology.
  • DOI:
    10.1016/j.jpsychires.2021.05.054
  • 发表时间:
    2021-08
  • 期刊:
  • 影响因子:
    4.8
  • 作者:
    Benatti, Beatrice;Dell'Osso, Bernardo;Shen, Hanyang;Filippou-Frye, Maria;Varias, Andrea;Sanchez, Catherine;Jo, Booil;Hollander, Eric;Fineberg, Naomi A.;Stein, Dan J.;Nicolini, Humberto;Lanzagorta, Nuria;Marazziti, Donatella;Pallanti, Stefano;Van Ameringen, Michael;Lochner, Christine;Karamustafalioglu, Oguz;Hranov, Luchezar;Figee, Martin;Drummond, Lynne;Grant, Jon E.;Denys, Damiaan;Fontenelle, Leonardo F.;Menchon, Jose M.;Zohar, Joseph;Pellegrini, Luca;Rodriguez, Carolyn I.
  • 通讯作者:
    Rodriguez, Carolyn I.
Meta-analysis of cognitive behaviour therapy and selective serotonin reuptake inhibitors for the treatment of hypochondriasis: Implications for trial design
  • DOI:
    10.1016/j.comppsych.2022.152334
  • 发表时间:
    2022-10-01
  • 期刊:
  • 影响因子:
    7.3
  • 作者:
    Fineberg, Naomi A.;Pellegrini, Luca;Laws, Keith R.
  • 通讯作者:
    Laws, Keith R.

Pellegrini, Luca的其他文献

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{{ truncateString('Pellegrini, Luca', 18)}}的其他基金

Micropeptides as a tool for intracellular signalling and regulation in higher eukaryotes
微肽作为高等真核生物细胞内信号传导和调节的工具
  • 批准号:
    238940-2006
  • 财政年份:
    2007
  • 资助金额:
    $ 2.04万
  • 项目类别:
    Discovery Grants Program - Individual
Micropeptides as a tool for intracellular signalling and regulation in higher eukaryotes
微肽作为高等真核生物细胞内信号传导和调节的工具
  • 批准号:
    238940-2006
  • 财政年份:
    2006
  • 资助金额:
    $ 2.04万
  • 项目类别:
    Discovery Grants Program - Individual
Biochemical characterization of a newly discovered family of highly conserved membrane proteins
新发现的高度保守膜蛋白家族的生化特征
  • 批准号:
    238940-2002
  • 财政年份:
    2005
  • 资助金额:
    $ 2.04万
  • 项目类别:
    Discovery Grants Program - Individual
Biochemical characterization of a newly discovered family of highly conserved membrane proteins
新发现的高度保守膜蛋白家族的生化特征
  • 批准号:
    238940-2002
  • 财政年份:
    2004
  • 资助金额:
    $ 2.04万
  • 项目类别:
    Discovery Grants Program - Individual
Biochemical characterization of a newly discovered family of highly conserved membrane proteins
新发现的高度保守膜蛋白家族的生化特征
  • 批准号:
    238940-2002
  • 财政年份:
    2003
  • 资助金额:
    $ 2.04万
  • 项目类别:
    Discovery Grants Program - Individual
Biochemical characterization of a newly discovered family of highly conserved membrane proteins
新发现的高度保守膜蛋白家族的生化特征
  • 批准号:
    238940-2002
  • 财政年份:
    2002
  • 资助金额:
    $ 2.04万
  • 项目类别:
    Discovery Grants Program - Individual

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Targeting ER-mitochondrial calcium signaling to promote healthier aging
靶向 ER 线粒体钙信号传导以促进更健康的衰老
  • 批准号:
    10443143
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    2022
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The mitochondrial rough-ER (mt-rER), a new type of endoplasmic reticulum: from structure to function
线粒体粗面-ER(mt-rER),一种新型内质网:从结构到功能
  • 批准号:
    RGPIN-2017-06130
  • 财政年份:
    2021
  • 资助金额:
    $ 2.04万
  • 项目类别:
    Discovery Grants Program - Individual
The mitochondrial rough-ER (mt-rER), a new type of endoplasmic reticulum: from structure to function
线粒体粗面-ER(mt-rER),一种新型内质网:从结构到功能
  • 批准号:
    RGPIN-2017-06130
  • 财政年份:
    2020
  • 资助金额:
    $ 2.04万
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    Discovery Grants Program - Individual
The mitochondrial rough-ER (mt-rER), a new type of endoplasmic reticulum: from structure to function
线粒体粗面-ER(mt-rER),一种新型内质网:从结构到功能
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