Abstract
Mitochondrial targeting of an Atp2-LacZ fusion protein confers a respiration-defective phenotype on yeast cells. This effect has been utilized to select strains that grow on nonfermentable carbon sources, some of which have decreased levels of hybrid protein localized to the organelle. Many of the mutants obtained were also temperature-sensitive for growth on all media. The recessive mft (mitochondrial fusion targeting) mutants have been assigned to three complementation groups. MFT1 was cloned and sequenced: it encodes a 255 amino acid protein that is highly basic and has no predicted membrane-spanning domains or organelle-targeting sequences. The MFT1 gene is 91% identical to an open reading frame 3' of the SIR3 gene. Evidence is presented that these two closely related genes could represent a recent gene duplication.
MeSH Terms
Amino Acid Sequence
Base Sequence
Cloning, Molecular
DNA, Fungal
DNA-Binding Proteins
Ethyl Methanesulfonate
Fungal Proteins/genetics,metabolism
Genes, Fungal
Genetic Complementation Test
Mitochondria/metabolism
Molecular Sequence Data
Mutation
Open Reading Frames
Oxygen Consumption/genetics
Phenotype
Recombinant Fusion Proteins/genetics,metabolism
Restriction Mapping
Saccharomyces cerevisiae/genetics,metabolism
Saccharomyces cerevisiae Proteins
Sequence Homology, Nucleic Acid
Temperature
Chemicals
DNA, Fungal
DNA-Binding Proteins
Fungal Proteins
Recombinant Fusion Proteins
Saccharomyces cerevisiae Proteins
MFT1 protein, S cerevisiae
Ethyl Methanesulfonate
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Garrett J M
Department of Biology, Hamilton College, Clinton, NY 13323.
Singh K K
Vonder Haar R A
Emr S D
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