Abstract
The cloning of cDNAs encoding murine 2-5A synthetase has identified three related transcripts, represented by a previously described cDNA clone, L3 and two novel cDNAs, L1 and L2. L1 contains an open reading frame coding for a protein that shows 70% conservation at the amino acid level when compared to the protein predicted to be encoded by L3. L2 recognizes an IFN-induced transcript 600-bp larger than the L3 transcript. These three cDNAs map to a cosmid, cII, containing two murine 2-5A synthetase genes, ME12 and ME5/ME8, situated in a head-to-tail orientation separated by approximately 8 kb. Southern analyses of ME12 and ME5/ME8 using L3, L1-specific and L2-specific probes indicate that these genes have a similar organization. cII was transiently and stably transfected into CV-1 cells. When treated with interferon, the transfected cells produced mature, murine 2-5A synthetase transcripts identified using L3 and L2-specific probes. Thus all transcripts present in IFN-treated mouse cells which are recognized by the available murine 2-5A synthetase cDNA probes map to an approximately 40 kb region of the mouse genome containing two 2-5A synthetase genes.
MeSH Terms
2',5'-Oligoadenylate Synthetase/genetics,metabolism
Amino Acid Sequence
Animals
Base Sequence
Blotting, Northern
Blotting, Southern
Cell Line
DNA
Genetic Linkage
Genomic Library
Interferons/pharmacology
Mice
Molecular Sequence Data
Open Reading Frames
Restriction Mapping
Sequence Homology, Nucleic Acid
Transcription, Genetic
Transfection
Chemicals
DNA
Interferons
2',5'-Oligoadenylate Synthetase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Rutherford M N
Research Institute, Hospital for Sick Children, Toronto, Canada.
Kumar A
Nissim A
Chebath J
Williams B R
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