A MUTATION OF FURIN CAUSES THE LACK OF PRECURSOR-PROCESSING ACTIVITY IN HUMAN COLON-CARCINOMA LOVO CELLS

被引:123
作者
TAKAHASHI, S
KASAI, K
HATSUZAWA, K
KITAMURA, N
MISUMI, Y
IKEHARA, Y
MURAKAMI, K
NAKAYAMA, K
机构
[1] UNIV TSUKUBA,INST BIOL SCI,TSUKUBA,IBARAKI 305,JAPAN
[2] UNIV TSUKUBA,INST APPL BIOCHEM,TSUKUBA,IBARAKI 305,JAPAN
[3] UNIV TSUKUBA,CTR GENE EXPT,TSUKUBA,IBARAKI 305,JAPAN
[4] KANSAI MED UNIV,INST LIVER RES,MORIGUCHI,OSAKA 570,JAPAN
[5] FUKUOKA UNIV,SCH MED,DEPT BIOCHEM,JONAN KU,FUKUOKA 81401,JAPAN
关键词
D O I
10.1006/bbrc.1993.2146
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
Furin has been proposed to be the endoprotease responsible for precursor cleavage at Arg-X-Lys/Arg-Arg (RXK/RR) sites within the constitutive secretory pathway. However, there was a possibility that other protease(s) is involved in this cleavage. We here characterized furin in human colon carcinoma LoVo cells, since these cells lacked the endogenous processing activity toward RXK/RR sites and recovered the activity by transfection of furin cDNA. Furin cDNA cloned from LoVo cells had one nucleotide deletion in the region covering the homo B domain which is essential for the endoproteolytic activity. LoVo cells transfected with a furin construct with the mutation showed no activity. Based on these data, we conclude that furin is the endoprotease that is involved in the cursor cleavage at RXK/RR sites within the constitutive secretory pathway. © 1993 Academic Press, Inc.
引用
收藏
页码:1019 / 1026
页数:8
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