Concurrent mutations in two different ras genes in acute myelocytic leukemias
Open Access
- 24 July 1987
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 15 (14) , 5669-5680
- https://doi.org/10.1093/nar/15.14.5669
Abstract
DNA transfection analyses (tumorigenicity assay) and hybridization to mutation specific oligonucleotide probes established point mutations in codon 61 of both, N-ras and Ki-ras genes in fresh leukemic cells of an AML patient. Concurrent activation of N-ras and Ki-ras sequences by point mutations in codons 12 were demonstrated for AML cell line Rc2a. Moreover, using a rapid and sensitive dot-blot screening procedure based on the combination of in vitro amplification of ras specific sequences and oligonucleotide hybridization we could show that ras gene activation was not present in primary leukemic cells of the patient this cell line had been derived from, but rather occurred during later passages of Rc2a.Keywords
This publication has 31 references indexed in Scilit:
- Ras p21 proteins with high or low GTPase activity can efficiently transform NIH3T3 cellsCell, 1986
- Biological and biochemical properties of human rasH genes mutated at codon 61Cell, 1986
- High Efficiency DNA-Mediated Transformation of Primate CellsScience, 1983
- Structure and organization of the human Ki-ras proto-oncogene and a related processed pseudogeneNature, 1983
- Identification of transforming gene in two human sarcoma cell lines as a new member of the ras gene family located on chromosome 1Nature, 1983
- Characterization of a human colon/lung carcinoma oncogeneNature, 1983
- Cellular Transforming GenesScience, 1982
- Cell lines derived from a human myelomonocytic leukaemiaBritish Journal of Haematology, 1982
- Tumorigenic transformation of mammalian cells induced by a normal human gene homologous to the oncogene of Harvey murine sarcoma virusNature, 1982
- Isolation and preliminary characterization of a human transforming gene from T24 bladder carcinoma cellsNature, 1982