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ATAD3A 寡聚化通过耦联线粒体片段化和生物能缺陷导致神经退行性变。

ATAD3A oligomerization causes neurodegeneration by coupling mitochondrial fragmentation and bioenergetics defects.

机构信息

Department of Physiology and Biophysics, Case Western Reserve University School of Medicine, Cleveland, OH, 44106, USA.

Case Cardiovascular Research Institute and Harrington Heart and Vascular Institute, Case Western Reserve University School of Medicine, Cleveland, OH, 44106, USA.

出版信息

Nat Commun. 2019 Mar 26;10(1):1371. doi: 10.1038/s41467-019-09291-x.

Abstract

Mitochondrial fragmentation and bioenergetic failure manifest in Huntington's disease (HD), a fatal neurodegenerative disease. The factors that couple mitochondrial fusion/fission with bioenergetics and their impacts on neurodegeneration however remain poorly understood. Our proteomic analysis identifies mitochondrial protein ATAD3A as an interactor of mitochondrial fission GTPase, Drp1, in HD. Here we show that, in HD, ATAD3A dimerization due to deacetylation at K135 residue is required for Drp1-mediated mitochondrial fragmentation. Disturbance of ATAD3A steady state impairs mtDNA maintenance by disrupting TFAM/mtDNA binding. Blocking Drp1/ATAD3A interaction with a peptide, DA1, abolishes ATAD3A oligomerization, suppresses mitochondrial fragmentation and mtDNA lesion, and reduces bioenergetic deficits and cell death in HD mouse- and patient-derived cells. DA1 treatment reduces behavioral and neuropathological phenotypes in HD transgenic mice. Our findings demonstrate that ATAD3A plays a key role in neurodegeneration by linking Drp1-induced mitochondrial fragmentation to defective mtDNA maintenance, suggesting that DA1 might be useful for developing HD therapeutics.

摘要

线粒体碎片化和生物能量衰竭表现在亨廷顿病(HD)中,这是一种致命的神经退行性疾病。然而,将线粒体融合/裂变与生物能量联系起来的因素及其对神经退行性变的影响仍知之甚少。我们的蛋白质组分析确定线粒体蛋白 ATAD3A 是 HD 中线粒体分裂 GTP 酶 Drp1 的相互作用蛋白。在这里,我们表明,在 HD 中,由于 K135 残基的去乙酰化,ATAD3A 二聚化是 Drp1 介导的线粒体碎片化所必需的。ATAD3A 稳态的破坏通过破坏 TFAM/mtDNA 结合来破坏 mtDNA 的维持。用肽 DA1 阻断 Drp1/ATAD3A 相互作用会使 ATAD3A 寡聚化,抑制线粒体碎片化和 mtDNA 损伤,并减少 HD 小鼠和患者来源细胞中的生物能量缺陷和细胞死亡。DA1 治疗可减少 HD 转基因小鼠的行为和神经病理学表型。我们的研究结果表明,ATAD3A 通过将 Drp1 诱导的线粒体碎片化与 mtDNA 维持缺陷联系起来,在神经退行性变中发挥关键作用,这表明 DA1 可能有助于开发 HD 治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac8/6435701/766dcd4297d0/41467_2019_9291_Fig1_HTML.jpg

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