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Structure of the human and murine R-ras genes, novel genes closely related to ras proto-oncogenes
Authors:D G Lowe  D J Capon  E Delwart  A Y Sakaguchi  S L Naylor  D V Goeddel
Institution:3. Department of Cellular and Structural Biology University of Texas Health Sciences Center San Antonio, Texas 78284 USA;1. Department of Pediatric Surgery, Tianjin Children''s Hospital, Tianjin, PR China;2. Department of Lung Cancer Surgery, Tianjin Medical University General Hospital, Heping District, Tianjin, China;1. Cancer Risk Factors and Lifestyle Epidemiology, Cancer Research and Prevention Institute (ISPO), Florence, Italy;2. Emergency Department, Gastroenterology, SOD2, AOU Careggi, Florence, Italy
Abstract:The human R-ras gene was isolated by low-stringency hybridization with a v-H-ras probe. The predicted 218 amino acid R-ras protein has an amino-terminal extension of 26 residues compared with H-ras p21, and shows 55% amino acid identity; conserved domains include the p21 GTP-binding site and the carboxy-terminal membrane localization sequence. R-ras has at least six exons, with the position of the first intron conserved relative to the Drosophila ras64B and Dictyostelium ras genes; there is no similarity in the exon-intron structure of the R-ras gene and of the mammalian H-, K-, and N-ras proto-oncogenes. Cloned mouse R-ras cDNAs exhibit 88% nucleotide and 94.5% predicted amino acid identity to human R-ras. Human R-ras was localized to chromosome 19, a site different from ras p21 genes. Mouse R-ras is syntenic with c-H-ras on chromosome 7.
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