Kotzbauer Paul T, Truax Adam C, Trojanowski John Q, Lee Virginia M-Y
Department of Neurology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
J Neurosci. 2005 Jan 19;25(3):689-98. doi: 10.1523/JNEUROSCI.4265-04.2005.
Mutations in the pantothenate kinase 2 (PANK2) gene have been identified in patients with neurodegeneration with brain iron accumulation (NBIA; formerly Hallervorden-Spatz disease). However, the mechanisms by which these mutations cause neurodegeneration are unclear, especially given the existence of multiple pantothenate kinase genes in humans and multiple PanK2 transcripts with potentially different subcellular localizations. We demonstrate that PanK2 protein is localized to mitochondria of neurons in human brain, distinguishing it from other pantothenate kinases that do not possess mitochondrial-targeting sequences. PanK2 protein translated from the most 5' start site is sequentially cleaved at two sites by the mitochondrial processing peptidase, generating a long-lived 48 kDa mature protein identical to that found in human brain extracts. The mature protein catalyzes the initial step in coenzyme A (CoA) synthesis but displays feedback inhibition in response to species of acyl CoA rather than CoA itself. Some, but not all disease-associated point mutations result in significantly reduced catalytic activity. The most common mutation, G521R, results in marked instability of the intermediate PanK2 isoform and reduced production of the mature isoform. These results suggest that NBIA is caused by altered neuronal mitochondrial lipid metabolism caused by mutations disrupting PanK2 protein levels and catalytic activity.
泛酸激酶2(PANK2)基因突变已在患有脑铁沉积神经退行性疾病(NBIA;原哈勒沃登-施帕茨病)的患者中被发现。然而,这些突变导致神经退行性变的机制尚不清楚,特别是考虑到人类中存在多个泛酸激酶基因以及多个具有潜在不同亚细胞定位的PanK2转录本。我们证明,PanK2蛋白定位于人类大脑神经元的线粒体中,这使其与其他不具有线粒体靶向序列的泛酸激酶区分开来。从最5'端起始位点翻译的PanK2蛋白被线粒体加工肽酶在两个位点依次切割,产生一种与在人类脑提取物中发现的相同的长寿命48 kDa成熟蛋白。该成熟蛋白催化辅酶A(CoA)合成的第一步,但对酰基辅酶A而非CoA本身的种类表现出反馈抑制。一些但并非所有与疾病相关的点突变会导致催化活性显著降低。最常见的突变G521R导致中间型PanK2异构体明显不稳定,并减少成熟异构体的产生。这些结果表明,NBIA是由突变破坏PanK2蛋白水平和催化活性导致的神经元线粒体脂质代谢改变所引起的。