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PINK1抑制局部蛋白质合成以限制有害线粒体DNA突变的传播。

PINK1 Inhibits Local Protein Synthesis to Limit Transmission of Deleterious Mitochondrial DNA Mutations.

作者信息

Zhang Yi, Wang Zong-Heng, Liu Yi, Chen Yong, Sun Nuo, Gucek Marjan, Zhang Fan, Xu Hong

机构信息

National Heart, Lung, and Blood Institute, NIH, Bethesda, MD 20892, USA.

National Heart, Lung, and Blood Institute, NIH, Bethesda, MD 20892, USA.

出版信息

Mol Cell. 2019 Mar 21;73(6):1127-1137.e5. doi: 10.1016/j.molcel.2019.01.013. Epub 2019 Feb 13.

Abstract

We have previously proposed that selective inheritance, the limited transmission of damaging mtDNA mutations from mother to offspring, is based on replication competition in Drosophila melanogaster. This model, which stems from our observation that wild-type mitochondria propagate much more vigorously in the fly ovary than mitochondria carrying fitness-impairing mutations, implies that germ cells recognize the fitness of individual mitochondria and selectively boost the propagation of healthy ones. Here, we demonstrate that the protein kinase PINK1 preferentially accumulates on mitochondria enriched for a deleterious mtDNA mutation. PINK1 phosphorylates Larp to inhibit protein synthesis on the mitochondrial outer membrane. Impaired local translation on defective mitochondria in turn limits the replication of their mtDNA and hence the transmission of deleterious mutations to the offspring. Our work confirms that selective inheritance occurs at the organelle level during Drosophila oogenesis and provides molecular entry points to test this model in other systems.

摘要

我们之前提出,选择性遗传,即有害的线粒体DNA(mtDNA)突变从母亲到后代的有限传递,是基于果蝇中的复制竞争。该模型源于我们的观察,即野生型线粒体在果蝇卵巢中的增殖比携带影响适应性突变的线粒体更为活跃,这意味着生殖细胞能够识别单个线粒体的适应性,并选择性地促进健康线粒体的增殖。在这里,我们证明蛋白激酶PINK1优先积累在富含有害mtDNA突变的线粒体上。PINK1使Larp磷酸化,以抑制线粒体外膜上的蛋白质合成。有缺陷的线粒体上局部翻译受损,进而限制了其mtDNA的复制,从而限制了有害突变向后代的传递。我们的工作证实了果蝇卵子发生过程中在细胞器水平上发生了选择性遗传,并提供了分子切入点,以便在其他系统中测试该模型。

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