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Mitochondrial protein import: isolation and characterization of the Saccharomyces cerevisiae MFT1 gene
Authors:Jinnie M. Garrett   Keshav K. Singh   R. A. Vonder Haar  Scott D. Emr
Affiliation:(1) Department of Biology, Hamilton College, 13323 Clinton, NY, USA;(2) Department of Biology, Texas A&M University, 77843 College Station, TX, USA;(3) Division of Biology, 147-75, California Institute of Technology, 91125 Pasadena, CA, USA;(4) Present address: Department of Immunology and Medical Microbiology, University of Florida College of Medicine, Box J-266 JHMHC, 32610 Gainesville, FL, USA
Abstract:Summary 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 3prime of the SIR3 gene. Evidence is presented that these two closely related genes could represent a recent gene duplication.The sequence reported here has been listed in the EMBL Data Library with Accession Number X55360.
Keywords:Yeast Saccharomyces cerevisiae  Mitochondrial protein import  MFT1  Gene fusions  Hybrid protein targeting
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