Ivatt Rachael M, Whitworth Alexander J
MRC Centre for Developmental and Biomedical Genetics; Sheffield, UK; Department of Biomedical Science; University of Sheffield; Sheffield, UK.
Autophagy. 2014 Aug;10(8):1476-7. doi: 10.4161/auto.29642. Epub 2014 Jun 27.
Mitochondrial quality control has an impact on many diseases, but intense research has focused on the action of 2 genes linked to heritable forms of Parkinson disease (PD), PINK1 and PARK2/parkin, which act in a common pathway to promote mitophagy. However, criticism has been raised that little evidence links this mechanism to sporadic PD. To gain a greater insight into the mechanisms of PINK1-PARK2 mediated mitophagy, we undertook a genome-wide RNAi screen in Drosophila and human cell models. Strikingly, we discovered several components of the lipogenesis pathway, including SREBF1, playing a conserved role in mitophagy. Our results suggest that lipids influence the stabilization of PINK1 during the initiation of mitophagy. Importantly, SREBF1 has previously been identified as a risk locus for sporadic PD, and thus implicates aberrant mitophagy as contributing to sporadic PD. Our findings suggest a role for lipid synthesis in PINK1-PARK2 mediated mitophagy, and propose a mechanistic link between familial and sporadic PD, supporting a common etiology.
线粒体质量控制对多种疾病都有影响,但大量研究集中在与帕金森病(PD)遗传形式相关的两个基因——PINK1和PARK2/parkin的作用上,它们在促进线粒体自噬的共同途径中发挥作用。然而,有人提出批评,认为几乎没有证据将这种机制与散发性PD联系起来。为了更深入了解PINK1 - PARK2介导的线粒体自噬机制,我们在果蝇和人类细胞模型中进行了全基因组RNA干扰筛选。令人惊讶的是,我们发现了脂肪生成途径的几个成分,包括SREBF1,它们在线粒体自噬中发挥着保守作用。我们的结果表明,脂质在自噬起始过程中影响PINK1的稳定性。重要的是,SREBF1此前已被确定为散发性PD的一个风险位点,因此表明异常的线粒体自噬导致散发性PD。我们的研究结果表明脂质合成在PINK1 - PARK2介导的线粒体自噬中发挥作用,并提出了家族性和散发性PD之间的机制联系,支持共同的病因学。