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斑马鱼(Danio rerio)早老素促进异常的β淀粉样肽生成,且其在淀粉样蛋白生成中的功能需要一个关键的天冬氨酸残基。

Zebrafish (Danio rerio) presenilin promotes aberrant amyloid beta-peptide production and requires a critical aspartate residue for its function in amyloidogenesis.

作者信息

Leimer U, Lun K, Romig H, Walter J, Grünberg J, Brand M, Haass C

机构信息

Department of Molecular Biology, Central Institute of Mental Health, Mannheim, Germany.

出版信息

Biochemistry. 1999 Oct 12;38(41):13602-9. doi: 10.1021/bi991453n.

Abstract

Alzheimer's disease (AD) is characterized by the invariable accumulation of senile plaques composed of amyloid beta-peptide (Abeta). Mutations in three genes are known to cause familial Alzheimer's disease (FAD). The mutations occur in the genes encoding the beta-amyloid precursor protein (betaAPP) and presenilin (PS1) and PS2 and cause the increased secretion of the pathologically relevant 42 amino acid Abeta42. We have now cloned the zebrafish (Danio rerio) PS1 homologue (zf-PS1) to study its function in amyloidogenesis and to prove the critical requirement of an unusual aspartate residue within the seventh putative transmembrane domain. In situ hybridization and reverse PCR reveal that zf-PS1 is maternally inherited and ubiquitously expressed during embryogenesis, suggesting an essential housekeeping function. zf-PS1 is proteolytically processed to produce a C-terminal fragment (CTF) of approximately 24 kDa similar to human PS proteins. Surprisingly, wt zf-PS1 promotes aberrant Abeta42 secretion like FAD associated human PS1 mutations. The unexpected pathologic activity of wt zf-PS1 may be due to several amino acid exchanges at positions where FAD-associated mutations have been observed. The amyloidogenic function of zf-PS1 depends on the conserved aspartate residue 374 within the seventh putative transmembrane domain. Mutagenizing this critical aspartate residue abolishes endoproteolysis of zf-PS1 and inhibits Abeta secretion in human cells. Inhibition of Abeta secretion is accompanied by the accumulation of C-terminal fragments of betaAPP, suggesting a defect in gamma-secretase activity. These data provide further evidence that PS proteins are directly involved in the proteolytic cleavage of betaAPP and demonstrate that this function is evolutionarily conserved.

摘要

阿尔茨海默病(AD)的特征是由β-淀粉样肽(Aβ)组成的老年斑不断积累。已知三个基因的突变会导致家族性阿尔茨海默病(FAD)。这些突变发生在编码β-淀粉样前体蛋白(βAPP)、早老素(PS1)和PS2的基因中,并导致具有病理相关性的42个氨基酸的Aβ42分泌增加。我们现已克隆了斑马鱼(Danio rerio)的PS1同源物(zf-PS1),以研究其在淀粉样蛋白生成中的功能,并证明第七个假定跨膜结构域内一个不寻常天冬氨酸残基的关键需求。原位杂交和逆转录PCR显示,zf-PS1是母系遗传的,在胚胎发育过程中广泛表达,提示其具有重要的管家功能。zf-PS1经过蛋白水解加工产生一个约24 kDa的C末端片段(CTF),类似于人类PS蛋白。令人惊讶的是,野生型zf-PS1像与FAD相关的人类PS1突变一样促进异常的Aβ42分泌。野生型zf-PS1意外的病理活性可能是由于在已观察到FAD相关突变的位置发生了几个氨基酸交换。zf-PS1的淀粉样蛋白生成功能取决于第七个假定跨膜结构域内保守的天冬氨酸残基374。诱变这个关键的天冬氨酸残基可消除zf-PS1的内蛋白水解作用,并抑制人类细胞中的Aβ分泌。Aβ分泌的抑制伴随着βAPP C末端片段的积累,提示γ-分泌酶活性存在缺陷。这些数据进一步证明PS蛋白直接参与βAPP的蛋白水解切割,并表明该功能在进化上是保守的。

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