A mutation of furin causes the lack of precursor-processing activity in human colon carcinoma LoVo cells

S Takahashi, K Kasai, K Hatsuzawa, N Kitamura… - Biochemical and …, 1993 - Elsevier
S Takahashi, K Kasai, K Hatsuzawa, N Kitamura, Y Misumi, Y Ikehara, K Murakami…
Biochemical and biophysical research communications, 1993Elsevier
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 …
Abstract
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 precursor cleavage at RXK/RR sites within the constitutive secretory pathway.
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