Molecular cloning of a novel mouse aspartic protease-like protein that is expressed abundantly in the kidney

被引:30
作者
Mori, K
Ogawa, Y
Tamura, N
Ebihara, K
Aoki, T
Muro, S
Ozaki, S
Tanaka, I
Tashiro, K
Nakao, K
机构
[1] KYOTO UNIV,GRAD SCH MED,DEPT MED & CLIN SCI,KYOTO 606,JAPAN
[2] KYOTO UNIV,GRAD SCH MED,DEPT MED CHEM,KYOTO 606,JAPAN
关键词
aspartic protease; cathepsin; signal sequence trap; (mouse kidney);
D O I
10.1016/S0014-5793(96)01473-1
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
By use of the signal sequence trap method, we isolated a cDNA encoding a novel aspartic protease-like protein from the mouse kidney, and termed it 'kidney-derived aspartic protease-like protein (KAP).' The protein, a 419-amino-acid polypeptide with a 16-amino-acid signal sequence, had 47% identity with mouse cathepsin D, and its overall structure was closely related to known aspartic proteases, Northern blot analysis revealed that KAP mRNA is expressed at the highest level in the kidney, at a moderate level in the lung, and at low levels in the spleen and adipose tissue, In situ hybridization analysis demonstrated that the mRNA is expressed abundantly in the proximal straight tubule and slightly, but significantly, in the proximal convoluted tubule in the kidney, This intra-renal distribution differs distinctly from those of previously reported proteases such as cathepsins B, D, and H.
引用
收藏
页码:218 / 222
页数:5
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