Institute of Neurogenetics, University of Lübeck, Lübeck.
Molecular Cellular and Developmental Biology Program, Division of Biology, Kansas State University, Manhattan, Kansas, USA.
Mov Disord. 2022 Nov;37(11):2284-2289. doi: 10.1002/mds.29183. Epub 2022 Aug 16.
X-linked dystonia-parkinsonism (XDP) is a neurodegenerative disorder caused by the intronic insertion of a SINE-VNTR-Alu (SVA) retrotransposon carrying an (AGAGGG) repeat expansion in the TAF1 gene. The molecular mechanisms by which this mutation causes neurodegeneration remain elusive.
We investigated whether (AGAGGG) repeats undergo repeat-associated non-AUG (RAN) translation, a pathogenic mechanism common among repeat expansion diseases.
XDP-specific RAN translation reporter plasmids were generated, transfected in HEK293 cells, and putative dipeptide repeat proteins (DPRs) were detected by Western blotting. Immunocytochemistry was performed in COS-7 cells to determine the subcellular localization of one DPR.
We detected putative DPRs from two reading frames, supporting the translation of poly-(Glu-Gly) and poly-(Arg-Glu) species. XDP RAN translation initiates within the (AGAGGG) sequence and poly-(Glu-Gly) DPRs formed nuclear inclusions in transfected cells.
In summary, our work provides the first in-vitro proof of principle that the XDP-linked (AGAGGG) repeat expansions can undergo RAN translation. © 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
X 连锁型肌张力障碍-帕金森病(XDP)是一种神经退行性疾病,由 TAF1 基因中 SINE-VNTR-Alu(SVA)反转座子的内含子插入携带(AGAGGG)重复扩展的序列引起。这种突变导致神经退行性变的分子机制仍不清楚。
我们研究了(AGAGGG)重复序列是否会发生重复相关的非 AUG(RAN)翻译,这是一种常见于重复扩展疾病的致病机制。
生成了 XDP 特异性 RAN 翻译报告质粒,转染 HEK293 细胞,并通过 Western blot 检测潜在的二肽重复蛋白(DPR)。在 COS-7 细胞中进行免疫细胞化学,以确定一种 DPR 的亚细胞定位。
我们从两个阅读框中检测到了潜在的 DPR,支持多(Glu-Gly)和多(Arg-Glu)物种的翻译。XDP RAN 翻译起始于(AGAGGG)序列内,并且在转染细胞中形成了核内包涵体的多(Glu-Gly)DPR。
总之,我们的工作首次提供了体外原理的证据,证明 XDP 相关的(AGAGGG)重复扩展可以进行 RAN 翻译。© 2022 作者。运动障碍协会代表国际帕金森病和运动障碍协会出版的《运动障碍》。