A Single Tyrosine Residue in the Amyloid Precursor Protein Intracellular Domain Is Essential for Developmental Function

被引:40
作者
Barbagallo, Alessia P. M. [1 ]
Wang, Zilai [2 ]
Zheng, Hui [2 ]
D'Adamio, Luciano [1 ,3 ]
机构
[1] Albert Einstein Coll Med, Dept Microbiol & Immunol, Bronx, NY 10461 USA
[2] Baylor Coll Med, Huffington Ctr Aging, Houston, TX 77030 USA
[3] Inst Cellular Biol & Neurobiol, Natl Res Council Italy, I-00143 Rome, Italy
基金
美国国家卫生研究院;
关键词
JNK-INTERACTING PROTEIN-1; NEURAL STEM-CELLS; FAMILY-MEMBERS; DEFICIENT MICE; APP; PHOSPHORYLATION; GENE; FE65; PROLIFERATION; GENERATION;
D O I
10.1074/jbc.C111.219873
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The A beta-precursor protein (APP) intracellular domain is highly conserved and contains many potentially important residues, in particular the (YENPTY687)-Y-682 motif. To dissect the functions of this sequence in vivo, we created an APP knock-in allele mutating Tyr(682) to Gly (Y682G). Crossing this allele to APP-like protein 2 (APLP2) knock-out background showed that mutation of Tyr(682) results in postnatal lethality and neuromuscular synapse defects similar to doubly deficient APP/APLP2 mice. Our results demonstrate that a single residue in the APP intracellular region, Tyr(682), is indispensable for the essential function of APP in developmental regulation.
引用
收藏
页码:8717 / 8721
页数:5
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