Nucleic Acids Research, 1984, Vol. 12, No. 18 6979-6993
© 1984
MOLECULAR BIOLOGY |
A human IFN-ß1, gene deleted of promoter sequences upstream from the TATA box is controlled post-transcriptionally by dsRNA
Department of Virology, Weizmann Institute of Science Rehovot, Israel
Received July 17, 1984. Revised September 10, 1984. Accepted September 10, 1984.
Induction of IFN-ß1 RNA was studied in the mouse cell line SR117-21E transformed by a BPV episome containing the human IFN-ß1 gene deleted of promoter sequences upstream from position 40. Nuclei isolated from these cells synthesize constitutively IFN-ß1 RNA from the partially deleted promoter. The IFN-ß1 RNA synthesized by nuclei of uninduced SR117-21E cells is similar to that made by nuclei of poly(rI):(rC)-induced cells, but does not accumulate and hence no IFN is produced unless the cells have been treated either by ds RNA or by cycloheximide. We conclude that the IFN-ß1 gene has, in addition to the transcription control due to upstream promoter sequences, an additional post-transcriptional control acting on mRNA accumulation and linked to sequences close to the TATA box and RNA start site. Both controls are relieved by ds RNA.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
D. Xu, K. Brumm, and L. Zhang The Latent Membrane Protein 1 of Epstein-Barr Virus (EBV) Primes EBV Latency Cells for Type I Interferon Production J. Biol. Chem., April 7, 2006; 281(14): 9163 - 9169. [Abstract] [Full Text] [PDF] |
||||
