Literature DB >> 3096566

The ras gene family.

D R Lowy, B M Willumsen.   

Abstract

Members of the ras multigene family have been found in virtually all eukaryotes, from yeast to mammals. ras is required for normal cell growth in the yeast Saccharomyces cerevisiae and in at least some mammalian cells. These genes induce tumorigenic transformation of established NIH 3T3 cells by increased expression of a normal ras gene, certain point mutations or amino acid deletion. In tumours, point mutation appears to be the most common mechanism of activation. The ras proteins are found at the plasma membrane, bind guanine nucleotides GDP and GTP and possess a GTPase activity. At least some ras proteins that have been activated by single amino acid substitutions possess a GTPase activity that is lower than that of the normal version. These results are consistent with the hypothesis that ras protein stimulates its putative target(s) when GTP is bound to it, as is true for the G regulatory proteins or elongation factor Tu. In Saccharomyces cerevisiae, ras has been shown to stimulate adenylate cyclase. However, there does not appear to be a direct interaction between ras and adenylate cyclase in mammalian cells.

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Year:  1986        PMID: 3096566

Source DB:  PubMed          Journal:  Cancer Surv        ISSN: 0261-2429


  11 in total

1.  The structure of the carboxyl terminus of the p21 protein. Structural relationship to the nucleotide-binding/transforming regions of the protein.

Authors:  P W Brandt-Rauf; R P Carty; J M Chen; G Lee; S Rackovsky; M R Pincus
Journal:  J Protein Chem       Date:  1990-04

Review 2.  Acylation of viral and eukaryotic proteins.

Authors:  R J Grand
Journal:  Biochem J       Date:  1989-03-15       Impact factor: 3.857

3.  Structure of the carboxyl terminus of the RAS gene-encoded P21 proteins.

Authors:  P W Brandt-Rauf; R P Carty; J Chen; M Avitable; J Lubowsky; M R Pincus
Journal:  Proc Natl Acad Sci U S A       Date:  1988-08       Impact factor: 11.205

4.  p21-ras effector domain mutants constructed by "cassette" mutagenesis.

Authors:  J C Stone; W C Vass; B M Willumsen; D R Lowy
Journal:  Mol Cell Biol       Date:  1988-08       Impact factor: 4.272

Review 5.  Cancer genes generated by rare chromosomal rearrangements rather than activation of oncogenes.

Authors:  P H Duesberg
Journal:  Med Oncol Tumor Pharmacother       Date:  1987

6.  Harvey murine sarcoma virus: influences of coding and noncoding sequences on cell transformation in vitro and oncogenicity in vivo.

Authors:  T J Velu; W C Vass; D R Lowy; P E Tambourin
Journal:  J Virol       Date:  1989-03       Impact factor: 5.103

Review 7.  Cancer genes: rare recombinants instead of activated oncogenes (a review).

Authors:  P H Duesberg
Journal:  Proc Natl Acad Sci U S A       Date:  1987-04       Impact factor: 11.205

8.  The Ras-GRF1 exchange factor coordinates activation of H-Ras and Rac1 to control neuronal morphology.

Authors:  Huibin Yang; Raymond R Mattingly
Journal:  Mol Biol Cell       Date:  2006-02-15       Impact factor: 4.138

9.  Characterization of mutagen-activated cellular oncogenes that confer anchorage independence to human fibroblasts and tumorigenicity to NIH 3T3 cells: sequence analysis of an enzymatically amplified mutant HRAS allele.

Authors:  C W Stevens; T H Manoharan; W E Fahl
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

10.  Schizosaccharomyces pombe ras1 and byr1 are functionally related genes of the ste family that affect starvation-induced transcription of mating-type genes.

Authors:  S A Nadin-Davis; A Nasim
Journal:  Mol Cell Biol       Date:  1990-02       Impact factor: 4.272

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