Suppr超能文献

一个内部的EELD结构域通过一条依赖Tom70的途径促进Mcl-1定位于线粒体。

An internal EELD domain facilitates mitochondrial targeting of Mcl-1 via a Tom70-dependent pathway.

作者信息

Chou Chiang-Hung, Lee Ru-Shuo, Yang-Yen Hsin-Fang

机构信息

Graduate Institute of Life Sciences, National Defense Medical Center, Taipei 114, Taiwan.

出版信息

Mol Biol Cell. 2006 Sep;17(9):3952-63. doi: 10.1091/mbc.e06-04-0319. Epub 2006 Jul 5.

Abstract

Mcl-1 functions at an apical step in many regulatory programs that control cell death. Although the mitochondrion is one major subcellular organelle where Mcl-1 functions, the molecular mechanism by which Mcl-1 is targeted to mitochondria remains unclear. Here, we demonstrate that Mcl-1 is loosely associated with the outer membrane of mitochondria. Furthermore, we demonstrate that Mcl-1 interacts with the mitochondrial import receptor Tom70, and such interaction requires an internal domain of Mcl-1 that contains an EELD motif. A Tom70 antibody that blocks Mcl-1-Tom70 interaction blocks mitochondrial import of Mcl-1 in vitro. Furthermore, Mcl-1 is significantly less targeted to mitochondria in Tom70 knockdown than in the control cells. Similar targeting preference is also observed for the DM mutant of Mcl-1 whose mutation at the EELD motif markedly attenuates its Tom70 binding activity. Together, our results indicate that the internal EELD domain facilitates mitochondrial targeting of Mcl-1 via a Tom70-dependent pathway.

摘要

Mcl-1在许多控制细胞死亡的调控程序的顶端步骤发挥作用。虽然线粒体是Mcl-1发挥功能的一个主要亚细胞器,但Mcl-1靶向线粒体的分子机制仍不清楚。在这里,我们证明Mcl-1与线粒体外膜松散结合。此外,我们证明Mcl-1与线粒体输入受体Tom70相互作用,这种相互作用需要Mcl-1的一个包含EELD基序的内部结构域。一种阻断Mcl-1-Tom70相互作用的Tom70抗体在体外阻断了Mcl-1的线粒体输入。此外,与对照细胞相比,在Tom70敲低的细胞中,Mcl-1靶向线粒体的能力显著降低。对于Mcl-1的DM突变体也观察到类似的靶向偏好,其EELD基序的突变显著减弱了其与Tom70的结合活性。总之,我们的结果表明,内部的EELD结构域通过Tom70依赖的途径促进Mcl-1靶向线粒体。

相似文献

1
An internal EELD domain facilitates mitochondrial targeting of Mcl-1 via a Tom70-dependent pathway.
Mol Biol Cell. 2006 Sep;17(9):3952-63. doi: 10.1091/mbc.e06-04-0319. Epub 2006 Jul 5.
2
Interaction between the human mitochondrial import receptors Tom20 and Tom70 in vitro suggests a chaperone displacement mechanism.
J Biol Chem. 2011 Sep 16;286(37):32208-19. doi: 10.1074/jbc.M111.280446. Epub 2011 Jul 19.
3
The fast-mobility isoform of mouse Mcl-1 is a mitochondrial matrix-localized protein with attenuated anti-apoptotic activity.
FEBS Lett. 2010 Aug 4;584(15):3323-30. doi: 10.1016/j.febslet.2010.07.013. Epub 2010 Jul 11.
4
Hsp90 functions in the targeting and outer membrane translocation steps of Tom70-mediated mitochondrial import.
J Biol Chem. 2006 Nov 3;281(44):33313-24. doi: 10.1074/jbc.M605250200. Epub 2006 Sep 12.
5
The C-terminal TPR domain of Tom70 defines a family of mitochondrial protein import receptors found only in animals and fungi.
J Mol Biol. 2006 May 12;358(4):1010-22. doi: 10.1016/j.jmb.2006.02.062. Epub 2006 Mar 20.
6
The N terminus of the anti-apoptotic BCL-2 homologue MCL-1 regulates its localization and function.
J Biol Chem. 2007 Nov 2;282(44):32233-42. doi: 10.1074/jbc.M706408200. Epub 2007 Sep 6.
7
Puma(*)Mcl-1 interaction is not sufficient to prevent rapid degradation of Mcl-1.
Oncogene. 2005 Nov 3;24(48):7224-37. doi: 10.1038/sj.onc.1208873.
8
Tetratricopeptide repeat proteins Tom70 and Tom71 mediate yeast mitochondrial morphogenesis.
EMBO Rep. 2008 Jan;9(1):63-9. doi: 10.1038/sj.embor.7401113. Epub 2007 Nov 16.
9
TOM70 Sustains Cell Bioenergetics by Promoting IP3R3-Mediated ER to Mitochondria Ca Transfer.
Curr Biol. 2018 Feb 5;28(3):369-382.e6. doi: 10.1016/j.cub.2017.12.047. Epub 2018 Jan 27.
10
Mouse Noxa uses only the C-terminal BH3-domain to inactivate Mcl-1.
Apoptosis. 2013 Sep;18(9):1093-105. doi: 10.1007/s10495-013-0868-9.

引用本文的文献

1
Chaperone-dependent and chaperone-independent functions of carboxylate clamp tetratricopeptide repeat (CC-TPR) proteins.
Trends Biochem Sci. 2025 Feb;50(2):121-133. doi: 10.1016/j.tibs.2024.11.004. Epub 2024 Dec 19.
2
Bcl-2 Family Members and the Mitochondrial Import Machineries: The Roads to Death.
Biomolecules. 2022 Jan 19;12(2):162. doi: 10.3390/biom12020162.
4
Contribution of Yeast Studies to the Understanding of BCL-2 Family Intracellular Trafficking.
Int J Mol Sci. 2021 Apr 15;22(8):4086. doi: 10.3390/ijms22084086.
7
identification and biochemical characterization of the human dicarboxylate clamp TPR protein interaction network.
FEBS Open Bio. 2018 Oct 9;8(11):1830-1843. doi: 10.1002/2211-5463.12521. eCollection 2018 Nov.
8
Leishmania donovani Exploits Myeloid Cell Leukemia 1 (MCL-1) Protein to Prevent Mitochondria-dependent Host Cell Apoptosis.
J Biol Chem. 2016 Feb 12;291(7):3496-507. doi: 10.1074/jbc.M115.672873. Epub 2015 Dec 15.
9
Calcium trafficking integrates endoplasmic reticulum function with mitochondrial bioenergetics.
Biochim Biophys Acta. 2014 Oct;1843(10):2233-9. doi: 10.1016/j.bbamcr.2014.03.022. Epub 2014 Mar 30.
10
Bcl-2 family in inter-organelle modulation of calcium signaling; roles in bioenergetics and cell survival.
J Bioenerg Biomembr. 2014 Feb;46(1):1-15. doi: 10.1007/s10863-013-9527-7.

本文引用的文献

1
Crystal structure of yeast mitochondrial outer membrane translocon member Tom70p.
Nat Struct Mol Biol. 2006 Jul;13(7):589-93. doi: 10.1038/nsmb1106. Epub 2006 Jun 11.
2
The C-terminal TPR domain of Tom70 defines a family of mitochondrial protein import receptors found only in animals and fungi.
J Mol Biol. 2006 May 12;358(4):1010-22. doi: 10.1016/j.jmb.2006.02.062. Epub 2006 Mar 20.
3
Proapoptotic Bak is sequestered by Mcl-1 and Bcl-xL, but not Bcl-2, until displaced by BH3-only proteins.
Genes Dev. 2005 Jun 1;19(11):1294-305. doi: 10.1101/gad.1304105. Epub 2005 May 18.
4
Stabilization and enhancement of the antiapoptotic activity of mcl-1 by TCTP.
Mol Cell Biol. 2005 Apr;25(8):3117-26. doi: 10.1128/MCB.25.8.3117-3126.2005.
7
Obligate role of anti-apoptotic MCL-1 in the survival of hematopoietic stem cells.
Science. 2005 Feb 18;307(5712):1101-4. doi: 10.1126/science.1106114.
9
Bcl-x(L) sequesters its C-terminal membrane anchor in soluble, cytosolic homodimers.
EMBO J. 2004 May 19;23(10):2146-55. doi: 10.1038/sj.emboj.7600225. Epub 2004 May 6.
10
Development and maintenance of B and T lymphocytes requires antiapoptotic MCL-1.
Nature. 2003 Dec 11;426(6967):671-6. doi: 10.1038/nature02067.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验