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PMID: 2424441 Published · ppublish English Journal Article

Cloning and expression in Escherichia coli of cDNA for arginase of rat liver.

Biochemical and biophysical research communications ·Vol. 136 ·No. 3 ·1986-05-14 ·Pages 955-61

Kawamoto S, Amaya Y, Oda T, Kuzumi T, Saheki T, Kimura S, Mori M

Abstract

A cDNA expression library constructed in a plasmid pUC8 from poly(A)+ RNA of rat liver was screened immunologically, using an antibody against arginase of rat liver. A cDNA clone was isolated and identified by hybrid-selected translation. The clone contained an insert approximately 1.35 kilobase pairs in length. In the bacterial clone, we detected a specific protein of Mr = about 43,000 that is slightly larger than the purified arginase (Mr = about 40,000) and a high activity of arginase was expressed. The arginase mRNA species of about 1600 bases long was detected in the liver, but not in the small intestine, kidney, spleen and heart of the rats.

MeSH Terms
Animals Cloning, Molecular DNA/metabolism DNA Restriction Enzymes/metabolism Electrophoresis, Polyacrylamide Gel Escherichia coli/enzymology,genetics Gene Expression Regulation Liver/enzymology Molecular Weight Nucleic Acid Hybridization Poly A/analysis RNA/analysis RNA, Messenger Rats
Chemicals
RNA, Messenger Poly A RNA DNA DNA Restriction Enzymes
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Kawamoto S
Amaya Y
Oda T
Kuzumi T
Saheki T
Kimura S
Mori M
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1986-05-14
Pages
955-61
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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