TY - JOUR
T1 - Genetic analysis of yeast RAS1 and RAS2 genes
AU - Kataoka, T.
AU - Powers, S.
AU - McGill, C.
AU - Fasano, O.
AU - Strathern, J.
AU - Broach, J.
AU - Wigler, M.
N1 - Funding Information:
This work was supported by grants from the National Institutes of Health and the American Business for Cancer Research Foundation, S. P. is a postdoctoral fellow of the Leukemia Society of America; T. K. is on leave from the Department of Genetics, Osaka University Medical School: J. B. is an Established Investigator of the American Heart Association; 0. F. is on leave from I lstituto di Chimica Biologica, II Facolta di Medicina, Universita di Napoli, Italy. We would like to thank J. Hicks, A. Klar, J. Ivy, M. Kelly, C. Stephens, and M. Zoller for useful discussions. We thank F. Tamanoi for preparation of the oligonucleotide.
PY - 1984/6
Y1 - 1984/6
N2 - We present a genetic analysis of RAS1 and RAS2 of S. cerevisiae, two genes that are highly homologous to mammalian ras genes. By constructing in vitro ras genes disrupted by selectable genes and introducing these by gene replacement into the respective ras loci, we have determined that neither RAS1 nor RAS2 are by themselves essential genes. However, rasl- ras2- spores of doubly heterozygous diploids are incapable of resuming vegetative growth. We have determined that RAS1 is located on chromosome XV, 7 cM from ade2 and 63 cM from his3; and RAS2 is located on chromosome XIV, 2 cM from met4. We have also constructed by site-directed mutagenesis a missense mutant, RAS2val19, which encodes valine in place of glycine at the nineteenth amino acid position, the same sort of missense mutation that is found in some transforming alleles of mammalian ras genes. Diploid yeast cells that contain this mutation are incapable of sporulating efficiently, even when they contain wild-type alleles.
AB - We present a genetic analysis of RAS1 and RAS2 of S. cerevisiae, two genes that are highly homologous to mammalian ras genes. By constructing in vitro ras genes disrupted by selectable genes and introducing these by gene replacement into the respective ras loci, we have determined that neither RAS1 nor RAS2 are by themselves essential genes. However, rasl- ras2- spores of doubly heterozygous diploids are incapable of resuming vegetative growth. We have determined that RAS1 is located on chromosome XV, 7 cM from ade2 and 63 cM from his3; and RAS2 is located on chromosome XIV, 2 cM from met4. We have also constructed by site-directed mutagenesis a missense mutant, RAS2val19, which encodes valine in place of glycine at the nineteenth amino acid position, the same sort of missense mutation that is found in some transforming alleles of mammalian ras genes. Diploid yeast cells that contain this mutation are incapable of sporulating efficiently, even when they contain wild-type alleles.
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U2 - 10.1016/0092-8674(84)90374-X
DO - 10.1016/0092-8674(84)90374-X
M3 - Article
C2 - 6327067
AN - SCOPUS:0021140814
VL - 37
SP - 437
EP - 445
JO - Cell
JF - Cell
SN - 0092-8674
IS - 2
ER -