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人源与鼠源tau蛋白N端的差异

Differences Between Human and Murine Tau at the N-terminal End.

作者信息

Hernández Félix, Merchán-Rubira Jesús, Vallés-Saiz Laura, Rodríguez-Matellán Alberto, Avila Jesús

机构信息

Network Center for Biomedical Research in Neurodegenerative Diseases (CIBERNED), Carlos III Institute of Health, Madrid, Spain.

Centro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas (CSIC), Universidad Autonoma de Madrid (UAM), Madrid, Spain.

出版信息

Front Aging Neurosci. 2020 Jan 28;12:11. doi: 10.3389/fnagi.2020.00011. eCollection 2020.

Abstract

Human tauopathies, such as Alzheimer's disease (AD), have been widely studied in transgenic mice overexpressing human tau in the brain. The longest brain isoforms of Tau in mice and humans show 89% amino acid identity; however, the expression of the isoforms of this protein in the adult brain of the two species differs. Tau 3R isoforms are not present in adult mice. In contrast, the adult human brain contains Tau 3R and also Tau 4R isoforms. In addition, the N-terminal sequence of Tau protein in mice and humans differs, a Tau peptide (residues 17-28) being present in the latter but absent in the former. Here we review the main published data on this N-terminal sequence that suggests that human and mouse Tau proteins interact with different endogenous proteins and also show distinct secretion patterns.

摘要

人类tau蛋白病,如阿尔茨海默病(AD),已在大脑中过表达人类tau蛋白的转基因小鼠中得到广泛研究。小鼠和人类大脑中最长的tau蛋白异构体显示出89%的氨基酸同一性;然而,该蛋白异构体在这两个物种成年大脑中的表达有所不同。tau 3R异构体在成年小鼠中不存在。相比之下,成年人类大脑中含有tau 3R以及tau 4R异构体。此外,小鼠和人类tau蛋白的N端序列不同,后者存在一个tau肽(第17 - 28位氨基酸残基),而前者不存在。在此,我们综述了关于该N端序列的主要已发表数据,这些数据表明人类和小鼠tau蛋白与不同的内源性蛋白相互作用,并且还表现出不同的分泌模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef85/6999090/ca3ab79d7989/fnagi-12-00011-g0001.jpg

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