McLaughlin Research Institute, 1520 23rd St S, Great Falls, MT, USA.
Mamm Genome. 2019 Jun;30(5-6):151-165. doi: 10.1007/s00335-019-09802-7. Epub 2019 May 14.
Spongiform encephalopathy is an intriguing yet poorly understood neuropathology characterized by vacuoles, demyelination, and gliosis. It is observed in patients with prion disease, primary mitochondrial disease, HIV-1 infection of the brain, and some inherited disorders, but the underlying mechanism of disease remains unclear. The brains of mice lacking the MGRN1 E3 ubiquitin ligase develop vacuoles by 9 months of age. MGRN1-dependent ubiquitination has been reported to regulate mitofusin 1 and GP78, suggesting MGRN1 may have a direct effect on mitochondrial homeostasis. Here, we demonstrate that some MGRN1 localizes to mitochondria, most likely due to N-myristoylation, and mitochondria in cells from Mgrn1 null mutant mice display fragmentation and depolarization without recruitment of the parkin E3 ubiquitin ligase. The late onset of pathology in the brains of Mgrn1 null mutant mice suggests that a further, age-dependent effect on mitochondrial homeostasis may be required to trigger vacuolation. Parkin protein and mRNA levels showed a significant decline in the brains of Mgrn1 null mutant mice by 12 months of age. To test whether loss of parkin triggers vacuolation through a synergistic effect, we generated Mgrn1; parkin double mutant mice. By 1 month of age, their brains demonstrated more severe mitochondrial dysfunction than Mgrn1 null mutants, but there was no effect on the age-of-onset of spongiform neurodegeneration. Expression of the ATF4 transcription factor, a key regulator of the mitochondrial stress response, also declined in the brains of aged Mgrn1 null mutant mice. Together, the data presented here indicate that loss of MGRN1 has early, direct effects on mitochondrial homeostasis and late, indirect effects on the ability of cells to respond to mitochondrial stress.
海绵状脑病是一种有趣但尚未被充分理解的神经病理学,其特征是有空泡、脱髓鞘和神经胶质增生。它发生在朊病毒病、原发性线粒体疾病、HIV-1 感染大脑和一些遗传性疾病患者中,但疾病的潜在机制仍不清楚。缺乏 MGRN1 E3 泛素连接酶的小鼠大脑在 9 个月大时就会出现空泡。据报道,MGRN1 依赖性泛素化可以调节线粒体融合蛋白 1 和 GP78,这表明 MGRN1 可能对线粒体稳态有直接影响。在这里,我们证明了一些 MGRN1 定位于线粒体,这很可能是由于 N-豆蔻酰化,而 Mgrn1 缺失突变小鼠细胞中的线粒体显示出碎片化和去极化,而没有募集 parkin E3 泛素连接酶。在 Mgrn1 缺失突变小鼠的大脑中,病理学的迟发性发作表明,可能需要进一步的、与年龄相关的对线粒体稳态的影响才能引发空泡化。Parkin 蛋白和 mRNA 水平在 Mgrn1 缺失突变小鼠的大脑中在 12 个月大时显著下降。为了测试 parkin 的缺失是否通过协同作用引发空泡化,我们生成了 Mgrn1; parkin 双突变小鼠。在 1 个月大时,它们的大脑表现出比 Mgrn1 缺失突变体更严重的线粒体功能障碍,但对海绵状神经退行性变的发病年龄没有影响。ATF4 转录因子的表达,一种线粒体应激反应的关键调节剂,也在年老的 Mgrn1 缺失突变小鼠的大脑中下降。总之,这里呈现的数据表明,MGRN1 的缺失对线粒体稳态有早期的直接影响,对细胞应对线粒体应激的能力有晚期的间接影响。