Cryo-EM structures of tau filaments from the brains of mice transgenic for human mutant P301S Tau.

IF 6.2 2区 医学 Q1 NEUROSCIENCES Acta Neuropathologica Communications Pub Date : 2023-10-05 DOI:10.1186/s40478-023-01658-y
Manuel Schweighauser, Alexey G Murzin, Jennifer Macdonald, Isabelle Lavenir, R Anthony Crowther, Sjors H W Scheres, Michel Goedert
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Abstract

Mice transgenic for human mutant P301S tau are widely used as models for human tauopathies. They develop neurodegeneration and abundant filamentous inclusions made of human mutant four-repeat tau. Here we used electron cryo-microscopy (cryo-EM) to determine the structures of tau filaments from the brains of Tg2541 and PS19 mice. Both lines express human P301S tau (0N4R for Tg2541 and 1N4R for PS19) on mixed genetic backgrounds and downstream of different promoters (murine Thy1 for Tg2541 and murine Prnp for PS19). The structures of tau filaments from Tg2541 and PS19 mice differ from each other and those of wild-type tau filaments from human brains. The structures of tau filaments from the brains of humans with mutations P301L, P301S or P301T in MAPT are not known. Filaments from the brains of Tg2541 and PS19 mice share a substructure at the junction of repeats 2 and 3, which comprises residues I297-V312 of tau and includes the P301S mutation. The filament core from the brainstem of Tg2541 mice consists of residues K274-H329 of tau and two disconnected protein densities. Two non-proteinaceous densities are also in evidence. The filament core from the cerebral cortex of line PS19 extends from residues G271-P364 of tau. One strong non-proteinaceous density is also present. Unlike the tau filaments from human brains, the sequences following repeat 4 are missing from the cores of tau filaments from the brains of Tg2541 and PS19 mice.

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来自转基因人类突变体P301S-tau的小鼠大脑的tau丝的冷冻EM结构。
转基因人类突变体P301S-tau的小鼠被广泛用作人类tau病的模型。它们发展为神经退行性变,并由人类突变的四重复tau组成大量丝状内含物。在这里,我们使用电子冷冻显微镜(cryo-EM)来确定Tg2541和PS19小鼠大脑中tau丝的结构。两个系在混合遗传背景和不同启动子的下游表达人P301S-tau(Tg2541为0N4R,PS19为1N4R)(Tg25421为鼠Thy1,PS19则为鼠Prnp)。来自Tg2541和PS19小鼠的tau丝的结构与来自人脑的野生型tau丝不同。来自MAPT中具有P301L、P301S或P301T突变的人类大脑的tau丝的结构尚不清楚。来自Tg2541和PS19小鼠大脑的细丝在重复序列2和3的连接处共享一个亚结构,该亚结构包括tau的残基I297-V312,并包括P301S突变。来自Tg2541小鼠脑干的丝核由tau的残基K274-H329和两个断开的蛋白质密度组成。两种非蛋白质密度也很明显。线PS19的来自大脑皮层的丝核从tau的残基G271-P364延伸。还存在一种强的非蛋白质密度。与人类大脑中的tau丝不同,重复序列4之后的序列在Tg2541和PS19小鼠大脑中的tau丝核心中缺失。
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来源期刊
Acta Neuropathologica Communications
Acta Neuropathologica Communications Medicine-Pathology and Forensic Medicine
CiteScore
11.20
自引率
2.80%
发文量
162
审稿时长
8 weeks
期刊介绍: "Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders. ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.
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