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Structure and nucleotide sequence of the 5' region of the human and feline c-sis proto-oncogenes

1986; Oxford University Press; Volume: 14; Issue: 2 Linguagem: Inglês

10.1093/nar/14.2.765

1362-4962

A. M.W. Van den Ouwcland, Anton Roebroek, Jack A. Schalken, C. A. A. Claesen, Henri P.J. Bloemers, Wim J.M. Van de Ven,

Genomics and Chromatin Dynamics

Comparative analysis of coamid clones containing the human and feline c- sis genetic regions revealed the similar structural organization of these areas in the two species. The areas shared seven different genetic regions in and around the c- sis locus and one of these was related to v- sis . Another region, 1.9 kbp in size and located about 8 kbp upstream of the v- sis homologous region in the human genome, also hybridized to the main c- sis transcriptional product of 3.5 kb. Comparison with a recently described c- sis cDNA clone (Collins et al ., Nature 316, 748–750 (1985)) revealed that the 1.9 kbp DNA region contained a large 5′ c- sis exon of at least 1050 bp. In this exon, the presumed initiation site of the predicted PDGF-2 containing precursor protein was located and appeared to be preceded by a large untranslated region. In the region Immediately upstream of this exon, a TATA box and a consensus sequence for a potential Sp1 binding site were found at similar positions in both species. This region also exhibited promoter activity when tested in an assay in which coding sequences of bacterial chloramphenicol acetyltransferase (CAT; acetyl-CoA: chloramphenicol 3-0-acetyltransferase, EC 2.3.1.28) were placed under its control. The five other DNA regions were found upstream and downstream of the human c- sis transcription unit and also in an intron. Four of them contained repetitive sequences. Hybridization analysis of human and feline c- sis containing cosmid clones with a mixed synthetic nucleotide probe, which corresponded to sequences encoding amino acid residues 2–7 of chain 1 of platelet-derived growth factor (PDGF-1), suggested that the c- sis cosmld clones did not include PDGF-1-specific genetic sequences.