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PMID: 1657897 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cloning and functional expression of a novel endoprotease involved in prohormone processing at dibasic sites.

Journal of biochemistry ·Vol. 109 ·No. 6 ·1991-06-00 ·Pages 803-6

Nakayama K, Hosaka M, Hatsuzawa K, Murakami K

Abstract

We cloned and sequenced a cDNA from a library of mouse pituitary AtT-20 cells which are known to cleave an endogenous and various foreign prohormones at dibasic sites. This cDNA encodes a novel 753-residue protein, named PC3, which is structurally related to the yeast Kex2 protease involved in precursor cleavage at dibasic sites and to recently identified mammalian Kex2-like proteins, furin and PC2. Among examined cell lines and tissues, PC3 mRNA was only detected in AtT-20 cells. The substrate specificity of PC3 expressed in mammalian cells was similar to that observed in AtT-20 cells. We conclude that PC3 is a resident prohormone processing endoprotease in AtT-20 cells.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Blotting, Northern Cell Line Cloning, Molecular DNA/genetics Gene Expression Regulation, Enzymologic Hormones/metabolism Mice Molecular Sequence Data Pro-Opiomelanocortin/biosynthesis,genetics Proprotein Convertases Receptors, Cell Surface/metabolism Serine Endopeptidases/genetics,metabolism Substrate Specificity
Chemicals
Hormones Receptors, Cell Surface Pro-Opiomelanocortin DNA Proprotein Convertases Serine Endopeptidases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Nakayama K
Institute of Biological Sciences, University of Tsukuba, Ibaraki.
Hosaka M
Hatsuzawa K
Murakami K
Article Info
Journal
Journal of biochemistry
Abbr.
J Biochem
ISSN
0021-924X
Published
1991-06-00
Pages
803-6
Language
English
Region
England
NLM ID
0376600
Subset
IM
Databases
GENBANK
M63255, M64332, S57661, S57664, S64490, S69601, S69604, S69828, S69830, X57088
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