| Literature DB >> 9573381 |
E Dosch1, B Zöller, I Redmann-Müller, I Nanda, M Schmid, A Viciano-Gofferge, C Jungwirth.
Abstract
The chicken interferon consensus sequence binding protein (ChICSBP) gene spans over 9 kb of DNA and consists, as its murine homolog, of nine exons. The first untranslated exon was identified by 5'-RACE technology. The second exon contains the translation initiation codon. Canonical consensus splice sites are found on every exon/intron junction. The introns are generally smaller than their mammalian counterparts. The ChICSBP and ChIRF-1 genes have been mapped by fluorescence in situ hybridization to different microchromosomes. The transcription start site has been mapped by primer extension. Inspection of the DNA sequence of a genomic clone containing the first exon and the region 1700-bp upstream revealed several potential cisregulatory elements of transcription. The ChICSBP mRNA is induced by recombinant ChIFN type I and ChIFN-gamma. A palindromic IFN regulatory element (pIRE) with high sequence homology to gamma activation site (GAS) sequences was functionally required in transient transfection assays for the induction of transcription by ChIFN-gamma.Entities:
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Year: 1998 PMID: 9573381 DOI: 10.1016/s0378-1119(98)00063-8
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688