- THIS ARTICLE
- Full Text (PDF)
- Alert me when this article is cited
- Alert me if a correction is posted
- SERVICES
- Similar articles in this journal
- Similar articles in PubMed
- Alert me to new issues of the journal
- Download to citation manager
- Reprints & Permissions
- CITING ARTICLES
- Citing Articles via Google Scholar
- GOOGLE SCHOLAR
- Articles by Barra, J. L.
- Articles by Rosa, A. L.
- Search for Related Content
- PUBMED
- PubMed Citation
- Articles by Barra, J. L.
- Articles by Rosa, A. L.
Genetics, Vol 144, 1455-1462, Copyright © 1996
INVESTIGATIONS |
A Dominant Negative Effect of eth-1(r), a Mutant Allele of the Neurospora crassa S-Adenosylmethionine Synthetase-Encoding Gene Conferring Resistance to the Methionine Toxic Analogue Ethionine
J. L. Barra, M. R. Mautino and A. L. Rosa
Present address: Institute de Genetique et Microbiologie, C.N.R.S., Universite de Paris-Sud, Bat. 400, 91405 Orsay Cedex, France.
eth-1(r), a thermosensitive allele of the Neurospora crassa S-adenosylmethionine (AdoMet) synthetase gene that confers ethionine resistance, has been cloned and sequenced. Replacement of an aspartic amino acid residue (D(48) -> N(48)), perfectly conserved in prokaryotic, fungal and higher eukaryotic AdoMet synthetases, was found responsible for both thermosensitivity and ethionine resistance conferred by eth-1(r). Gene fusion constructs, designed to overexpress eth-1(r) in vivo, render transformant cells resistant to ethionine. Dominance of ethionine resistance was further demonstrated in eth-1(+)/eth-1(r) partial diploids carrying identical gene doses of both alleles. Heterozygous eth-1(+)/eth-1(r) cells have, at the same time, both the thermotolerance conferred by eth-1(+) and the ethionine-resistant phenotype conferred by eth-1(r). AdoMet levels and AdoMet synthetase activities were dramatically decreased in heterozygous eth-1(+)/eth-1(r) cells. We propose that this negative effect exerted by eth-1(r) results from the in vivo formation of heteromeric eth-1(+)/eth-1(r) AdoMet synthetase molecules.