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人类朊病毒蛋白(PrP)219K可转化为PrPSc,但在变异型克雅氏病感染中表现出杂合抑制作用。

Human prion protein (PrP) 219K is converted to PrPSc but shows heterozygous inhibition in variant Creutzfeldt-Jakob disease infection.

作者信息

Hizume Masaki, Kobayashi Atsushi, Teruya Kenta, Ohashi Hiroaki, Ironside James W, Mohri Shirou, Kitamoto Tetsuyuki

机构信息

Division of CJD Science and Technology, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan.

出版信息

J Biol Chem. 2009 Feb 6;284(6):3603-9. doi: 10.1074/jbc.M809254200. Epub 2008 Dec 10.

Abstract

Prion protein gene (PRNP) E219K is a human polymorphism commonly occurring in Asian populations but is rarely found in patients with sporadic Creutzfeldt-Jakob disease (CJD). Thus the polymorphism E219K has been considered protective against sporadic CJD. The corresponding mouse prion protein (PrP) polymorphism variant (mouse PrP 218K) is not converted to the abnormal isoform (PrP(Sc)) and shows a dominant negative effect on wild-type PrP conversion. To define the conversion activity of this human molecule, we herein established knock-in mice with human PrP 219K and performed a series of transmission experiments with human prions. Surprisingly, the human PrP 219K molecule was converted to PrP(Sc) in variant CJD infection, and the conversion occurred more efficiently than PrP 219E molecule. Notably the knock-in mice with PRNP codon 219E/K showed the least efficient conversion compared with their hemizygotes with PRNP codon 219E/0 or codon 219K/0, or homozygotes with PRNP codon 219E/E or codon 219K/K. This phenomenon indicated heterozygous inhibition. This heterozygous inhibition was observed also in knock-in mice with PRNP codon 129M/V genotype. In addition to variant CJD infection, the human PrP 219K molecule is conversion-competent in transmission experiments with sporadic CJD prions. Therefore, the protective effect of PRNP E219K against sporadic CJD might be due to heterozygous inhibition.

摘要

朊病毒蛋白基因(PRNP)E219K是一种常见于亚洲人群的人类多态性,但在散发性克雅氏病(CJD)患者中很少见。因此,E219K多态性被认为对散发性CJD具有保护作用。相应的小鼠朊病毒蛋白(PrP)多态性变体(小鼠PrP 218K)不会转化为异常异构体(PrP(Sc)),并对野生型PrP转化表现出显性负效应。为了确定这种人类分子的转化活性,我们在此建立了携带人类PrP 219K的基因敲入小鼠,并用人朊病毒进行了一系列传播实验。令人惊讶的是,人类PrP 219K分子在变异型CJD感染中转化为PrP(Sc),并且转化比PrP 219E分子更有效。值得注意的是,与携带PRNP密码子219E/0或密码子219K/0的半合子,或携带PRNP密码子219E/E或密码子219K/K的纯合子相比,携带PRNP密码子219E/K的基因敲入小鼠的转化效率最低。这种现象表明存在杂合抑制。在携带PRNP密码子129M/V基因型的基因敲入小鼠中也观察到了这种杂合抑制。除了变异型CJD感染外,人类PrP 219K分子在散发性CJD朊病毒的传播实验中也具有转化能力。因此,PRNP E219K对散发性CJD的保护作用可能是由于杂合抑制。

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