共 52 条
A NOVEL SPECIES-SPECIFIC RNA RELATED TO ALTERNATIVELY SPLICED AMYLOID PRECURSOR PROTEIN MESSENGER-RNAS
被引:40
作者:

JACOBSEN, JS
论文数: 0 引用数: 0
h-index: 0
机构: Molecular Neurobiology Group, Central Nervous System Biological Research Department, Medical Research Division Lederle Laboratories Division, Pearl River

MUENKEL, HA
论文数: 0 引用数: 0
h-index: 0
机构: Molecular Neurobiology Group, Central Nervous System Biological Research Department, Medical Research Division Lederle Laboratories Division, Pearl River

BLUME, AJ
论文数: 0 引用数: 0
h-index: 0
机构: Molecular Neurobiology Group, Central Nervous System Biological Research Department, Medical Research Division Lederle Laboratories Division, Pearl River

VITEK, MP
论文数: 0 引用数: 0
h-index: 0
机构: Molecular Neurobiology Group, Central Nervous System Biological Research Department, Medical Research Division Lederle Laboratories Division, Pearl River
机构:
[1] Molecular Neurobiology Group, Central Nervous System Biological Research Department, Medical Research Division Lederle Laboratories Division, Pearl River
关键词:
ALZHEIMERS DISEASE;
ALTERNATIVE MESSENGER RNA SPLICING;
AMYLOID;
AMYLOID PRECURSOR PROTEIN;
AMYLOID PRECURSOR-RELATED PROTEIN;
BETA-AMYLOID PEPTIDE;
TRANSCRIPT QUANTITATION;
S1-PROTECTION ANALYSIS;
D O I:
10.1016/0197-4580(91)90089-3
中图分类号:
R592 [老年病学];
C [社会科学总论];
学科分类号:
03 ;
0303 ;
100203 ;
摘要:
Using an S1 nuclease protection assay, we have identified a novel "variant" Amyloid Precursor Protein (APP) RNA in human brain which is 3-6-fold more abundant than APP-770, but less abundant than APP-751 or APP-695. This variant, referred to as amyloid precursor-related protein 365 (APRP-365), is not detected in mouse and rat brain RNAs. A 1.6 kilo-basepair cDNA clone corresponding to this variant APP RNA predicts the existence of a 365 amino acid protein that is similar to the amino-terminal end of APP-770 but lacks the beta-amyloid peptide and any hydrophobic transmembrane spanning domains. In a modified polymerase chain reaction (PCR), we used amplification of reverse transcribed mRNA to confirm and extend our S1 observations. Together, the features of APRP-365 suggest that the human variant is a soluble protein containing a Kunitz protease inhibitor domain.
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页码:575 / 583
页数:9
相关论文
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