Markham Briana N, Ramnarine Chloe, Kim Songeun, Grever William E, Soto-Beasley Alexandra I, Heckman Michael, Ren Yingxue, Osborne Andrew C, Bhagwate Aditya V, Liu Yuanhang, Wang Chen, Kim Jungsu, Wszolek Zbigniew K, Ross Owen A, Springer Wolfdieter, Fiesel Fabienne C
Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA.
Revvity, Waltham, MA 02451, USA.
bioRxiv. 2024 Jan 19:2024.01.17.576122. doi: 10.1101/2024.01.17.576122.
Loss-of-function mutations in the genes encoding PINK1 and PRKN result in early-onset Parkinson disease (EOPD). Together the encoded enzymes direct a neuroprotective pathway that ensures the elimination of damaged mitochondria via autophagy. We performed a genome-wide high content imaging miRNA screen for inhibitors of the PINK1-PRKN pathway and identified all three members of the miRNA family 29 (miR-29). Using RNAseq we identified target genes and found that siRNA against ATG9A phenocopied the effects of miR-29 and inhibited the initiation of PINK1-PRKN mitophagy. Furthermore, we discovered two rare, potentially deleterious, missense variants (p.R631W and p.S828L) in our EOPD cohort and tested them experimentally in cells. While expression of wild-type ATG9A was able to rescue the effects of miR-29a, the EOPD-associated variants behaved like loss-of-function mutations. Together, our study validates miR-29 and its target gene ATG9A as novel regulators of mitophagy initiation. It further serves as proof-of-concept of finding novel, potentially disease-causing EOPD-linked variants specifically in mitophagy regulating genes. The nomination of genetic variants and biological pathways is important for the stratification and treatment of patients that suffer from devastating diseases, such as EOPD.
编码PINK1和PRKN的基因功能丧失突变会导致早发性帕金森病(EOPD)。这两种编码酶共同指导一条神经保护途径,通过自噬确保清除受损的线粒体。我们针对PINK1-PRKN途径的抑制剂进行了全基因组高内涵成像miRNA筛选,并鉴定出miRNA家族29(miR-29)的所有三个成员。通过RNA测序,我们确定了靶基因,发现针对ATG9A的小干扰RNA(siRNA)模拟了miR-29的作用,并抑制了PINK1-PRKN线粒体自噬的启动。此外,我们在EOPD队列中发现了两个罕见的、可能有害的错义变体(p.R631W和p.S828L),并在细胞中进行了实验测试。虽然野生型ATG9A的表达能够挽救miR-29a的作用,但与EOPD相关的变体表现得像功能丧失突变。总之,我们的研究验证了miR-29及其靶基因ATG9A是线粒体自噬启动的新型调节因子。它进一步证明了在调节线粒体自噬的基因中寻找新的、可能导致疾病的EOPD相关变体的概念。确定遗传变体和生物学途径对于患有诸如EOPD等毁灭性疾病的患者的分层和治疗非常重要。