Chou Chiang-Hung, Lee Ru-Shuo, Yang-Yen Hsin-Fang
Graduate Institute of Life Sciences, National Defense Medical Center, Taipei 114, Taiwan.
Mol Biol Cell. 2006 Sep;17(9):3952-63. doi: 10.1091/mbc.e06-04-0319. Epub 2006 Jul 5.
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.
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。