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PMID: 3754863 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Structure and expression of a cloned cDNA for human (2'-5')oligoadenylate synthetase.

Journal of biochemistry ·Vol. 99 ·No. 5 ·1986-05-00 ·Pages 1455-64

Shiojiri S, Fukunaga R, Ichii Y, Sokawa Y

Abstract

17S poly(A)+RNA, which hybridized to an oligonucleotide complementary to a part of the partial cDNA (E1cDNA) (Merlin et al. (1983) Proc. Natl. Acad. Sci. U.S. 80, 4904) for 2-5A synthetase, was isolated from interferon-treated human KB cells and used for cDNA cloning. Several overlapping cDNAs were cloned by using the oligonucleotide as a probe. Two of them were joined at their overlapping region, resulting in a cDNA (22-1 cDNA) of 1.4 kb containing a long open reading frame. When the cDNA was expressed in COS-7 cells with an eukaryotic promoter, active 2-5A synthetase was produced and localized mainly in the cytoplasm. The 5'-proximal ATG in 22-1 cDNA is followed immediately by another ATG. This second ATG was assumed to work as the initiator codon. If so, this enzyme comprises 363 amino acids.

MeSH Terms
2',5'-Oligoadenylate Synthetase/biosynthesis,genetics Amino Acid Sequence Base Sequence Cell Line Cloning, Molecular Codon/metabolism DNA Humans Nucleic Acid Hybridization Plasmids RNA, Messenger/metabolism
Chemicals
Codon RNA, Messenger DNA 2',5'-Oligoadenylate Synthetase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Shiojiri S
Fukunaga R
Ichii Y
Sokawa Y
Article Info
Journal
Journal of biochemistry
Abbr.
J Biochem
ISSN
0021-924X
Published
1986-05-00
Pages
1455-64
Language
English
Region
England
NLM ID
0376600
Subset
IM
Databases
GENBANK
D00068, N00068
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