Abstract
A hybrid plasmid was constructed from pSV2-Ecogpt (Mulligan and Berg, 1981) and the cloned 1.8 kilobase chromosomal DNA segment which contains the human interferon (HIFN-beta 1) gene and its flanking sequences. Cultured mouse FM3A cells were transfected by the hybrid plasmid and several Ecogpt+ clones were selected. Southern blot analysis of the DNA from these mouse cell clones showed that two of them contained a few copies of the 1.8 kilobase human DNA. Synthesis of mRNA characteristic of the HIFN-beta 1 mRNA increased as measured by RNA blot analysis when those clones were treated with Newcastle disease virus or with poly(I):poly(C). In addition, the induced mouse cell clones gave rise to the synthesis of human IFN-beta 1. These results suggest the presence of a unique nucleotide sequence in the 1.8 kilobase DNA which is sufficient for the inducer-responsive expression of the human IFN-beta 1 gene.
MeSH Terms
Animals
Base Sequence
Cell Line
Cloning, Molecular
DNA Restriction Enzymes
Female
Genes
Humans
Interferons/genetics
Mammary Neoplasms, Experimental/immunology
Mice
Newcastle disease virus/immunology
Nucleic Acid Hybridization
Plasmids
Poly I-C/pharmacology
Protein Biosynthesis
RNA, Messenger/genetics
Transcription, Genetic
Chemicals
RNA, Messenger
Interferons
DNA Restriction Enzymes
Poly I-C
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ohno S
Taniguchi T
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