Genetics, Vol. 151, 1353-1363, April 1999, Copyright © 1999
Suppression of a Nuclear aep2 Mutation in Saccharomyces cerevisiae by a Base Substitution in the 5'-Untranslated Region of the Mitochondrial oli1 Gene Encoding Subunit 9 of ATP Synthase
Timothy P. Ellisa,
H. Bruce Lukinsa,
Phillip Nagleya, and
Brian E. Cornera
a Department of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria 3168, Australia
Corresponding author:
Phillip Nagley, Department of Biochemistry and Molecular Biology, Monash University, Clayton, VIC 3168, Australia., phillip.nagley{at}med.monash.edu.au (E-mail)
Communicating editor: A. G. HINNEBUSCH
Mutations in the nuclear AEP2 gene of Saccharomyces generate greatly reduced levels of the mature form of mitochondrial oli1 mRNA, encoding subunit 9 of mitochondrial ATP synthase. A series of mutants was isolated in which the temperature-sensitive phenotype resulting from the aep2-ts1 mutation was suppressed. Three strains were classified as containing a mitochondrial suppressor: these lost the ability to suppress aep2-ts1 when their mitochondrial genome was replaced with wild-type mitochondrial DNA (mtDNA). Many other isolates were classified as containing dominant nuclear suppressors. The three mitochondrion-encoded suppressors were localized to the oli1 region of mtDNA using rho- genetic mapping techniques coupled with PCR analysis; DNA sequencing revealed, in each case, a T-to-C nucleotide transition in mtDNA 16 nucleotides upstream of the oli1 reading frame. It is inferred that the suppressing mutation in the 5' untranslated region of oli1 mRNA restores subunit 9 biosynthesis by accommodating the modified structure of Aep2p generated by the aep2-ts1 mutation (shown here to cause the substitution of proline for leucine at residue 413 of Aep2p). This mode of mitochondrial suppression is contrasted with that mediated by heteroplasmic rearranged rho- mtDNA genomes bypassing the participation of a nuclear gene product in expression of a particular mitochondrial gene. In the present study, direct RNA-protein interactions are likely to form the basis of suppression.
