Binding of APC to the human homolog of the Drosophila discs large tumor suppressor protein

被引:393
作者
Matsumine, A
Ogai, A
Senda, T
Okumura, N
Satoh, K
Baeg, GH
Kawahara, T
Kobayashi, S
Okada, M
Toyoshima, K
Akiyama, T
机构
[1] OSAKA UNIV,MICROBIAL DIS RES INST,DEPT ONCOGENE RES,SUITA,OSAKA 565,JAPAN
[2] NAGOYA UNIV,SCH MED,DEPT ANAT 1,NAGOYA,AICHI 466,JAPAN
[3] OSAKA UNIV,INST PROT RES,DIV PROT METAB,SUITA,OSAKA 565,JAPAN
[4] CTR ADULT DIS,OSAKA 537,JAPAN
关键词
D O I
10.1126/science.272.5264.1020
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The adenomatous polyposis coli gene (APC) is mutated in familial adenomatous polyposis and in sporadic colorectal tumors, and its product binds to the adherens junction protein beta-catenin. Overexpression of APC blocks cell cycle progression, The APC-beta-catenin complex was shown to bind to DLG, the human homolog of the Drosophila discs large tumor suppressor protein, This interaction required the carboxyl-terminal region of APC and the DLG homology repeat region of DLG. APC colocalized with DLG at the lateral cytoplasm in rat colon epithelial cells and at the synapse in cultured hippocampal neurons. These results suggest that the APC-DLG complex may participate in regulation of both cell cycle progression and neuronal function.
引用
收藏
页码:1020 / 1023
页数:4
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