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
- 来源:
- 关键词:
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.**
细胞器间接触位点几乎存在于细胞的所有区室之间,由于越来越多的生理和代谢过程是通过细胞器之间的物理相互作用来协调的,因此对细胞器间接触位点的研究已成为非常热门的话题。最具特征的细胞器间接触类型之一是发生在线粒体和光滑体之间的接触,它用于交换钙和调节呼吸,Ca2+稳态和信号传导,磷脂生物合成等。然而,可以发现线粒体也与含有核糖体的rough相关,但这种关联的功能尚不清楚,并且这种线粒体相关的rough (mt-rER)是否是一种特殊类型的ER仍有待确定。******在这里,我们分享了大量令人信服的初步数据,提出了一项研究计划,其目的是表明mt-内质网是一种结构独特的内质网,通过翻译和划分其途径的酶和运输它们的脂蛋白来控制胆固醇和脂肪酸的合成。******为了实现这一目标,我们将利用一项特别开发的协议,允许小鼠肝脏mt-rER的纯化,并利用我们在低温电子显微镜,低温电子断层扫描,3D成像,转录组学和蛋白质组学方面的经验来显示:******1:mt-rER不连接到细胞的ER网络***2:mt-rER具有与ER不同的蛋白质组***3。平滑体和线粒体之间的接触部位(称为MAM或MERC)是mt-rER***4的一个亚结构域;脂质和胆固醇途径的蛋白质直接在mt-rER***5上翻译;脂质和胆固醇途径的蛋白质定位在mt-rER和线粒体之间的界面上***6:mt-rER含有活性的胆固醇生物合成途径。******最终,这项研究将表明mt-rER和线粒体之间的并列作用于划分底物、酶和脂质和胆固醇途径的前体,从而解释细胞如何有效地合成、处理和运输大量这些分子。******这些发现将对许多人产生重大影响。对于细胞生物学家来说,因为他们将建立mt-rER作为一种新的,结构和功能独特的ER类型;对于细胞生理学家来说,因为他们认为mt-rER在通过脂蛋白的合成使脂质和胆固醇进入循环中起着关键作用;以及MAM/MERC领域的研究人员,因为他们将为研究调节这一重要亚细胞区室的生物发生和重塑的机制提供一个框架
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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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
Insights into Fanconi Anaemia from the structure of human FANCE
- DOI:
10.1093/nar/gkm033 - 发表时间:
2007-01-01 - 期刊:
- 影响因子:14.9
- 作者:
Nookala, Ravi K.;Hussain, Shobbir;Pellegrini, Luca - 通讯作者:
Pellegrini, Luca
A Mitofusin-2-dependent inactivating cleavage of Opa1 links changes in mitochondria cristae and ER contacts in the postprandial liver
- DOI:
10.1073/pnas.1408061111 - 发表时间:
2014-11-11 - 期刊:
- 影响因子:11.1
- 作者:
Sood, Aditi;Jeyaraju, Danny Vijey;Pellegrini, Luca - 通讯作者:
Pellegrini, Luca
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.
Phosphorylation and cleavage of presenilin-associated rhomboid-like protein (PARL) promotes changes in mitochondrial morphology
- DOI:
10.1073/pnas.0604983103 - 发表时间:
2006-12-05 - 期刊:
- 影响因子:11.1
- 作者:
Jeyaraju, Danny V.;Xu, Liqun;Pellegrini, Luca - 通讯作者:
Pellegrini, Luca
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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