A DNA Helicase Required for Maintenance of the Functional Mitochondrial Genome in Saccharomyces cerevisiae

ABSTRACT A novel DNA helicase, a homolog of several prokaryotic helicases, including Escherichia coli Rep and UvrD proteins, is encoded by the Saccharomyces cerevisiae nuclear genome open reading frame YOL095c on the chromosome XV. Our data demonstrate that the helicase is localized in the yeast mitochondria and is loosely associated with the mitochondrial inner membrane during biochemical fractionation. The sequence of the C-terminal end of the 80-kDa helicase protein is similar to a typical N-terminal mitochondrial targeting signal; deletions and point mutations in this region abolish transport of the protein into mitochondria. The C-terminal signal sequence of the helicase targets a heterologous carrier protein into mitochondria in vivo. The purified recombinant protein can unwind duplex DNA molecules in an ATP-dependent manner. The helicase is required for the maintenance of the functional ([rho+]) mitochondrial genome on both fermentable and nonfermentable carbon sources. However, the helicase is not essential for the maintenance of several defective ([rho −]) mitochondrial genomes. We also demonstrate that the helicase is not required for transcription in mitochondria.

[1]  D. Lockshon,et al.  A role for recombination junctions in the segregation of mitochondrial DNA in yeast , 1995, Cell.

[2]  D. Denhardt,et al.  The single-stranded DNA phages. , 1975, CRC critical reviews in microbiology.

[3]  M. Lunt Single-stranded DNA phages , 1980, Nature.

[4]  J. Bargonetti,et al.  Staphylococcus aureus chromosomal mutations that decrease efficiency of Rep utilization in replication of pT181 and related plasmids , 1989, Journal of bacteriology.

[5]  J. Diffley,et al.  A close relative of the nuclear, chromosomal high-mobility group protein HMG1 in yeast mitochondria. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[6]  W. L. Fangman,et al.  A nuclear mutation reversing a biased transmission of yeast mitochondrial DNA. , 1991, Genetics.

[7]  Eugene V. Koonin,et al.  Helicases: amino acid sequence comparisons and structure-function relationships , 1993 .

[8]  F. Foury,et al.  PIF1 DNA helicase from Saccharomyces cerevisiae. Biochemical characterization of the enzyme. , 1993, The Journal of biological chemistry.

[9]  R. Rothstein,et al.  The genetic control of direct-repeat recombination in Saccharomyces: the effect of rad52 and rad1 on mitotic recombination at GAL10, a transcriptionally regulated gene. , 1989, Genetics.

[10]  A. Bardwell,et al.  Dual roles of a multiprotein complex from S. cerevisiae in transcription and DNA repair , 1993, Cell.

[11]  M. Roberti,et al.  DNA-helicase activity from sea urchin mitochondria. , 1996, Biochemical and biophysical research communications.

[12]  D. Denhardt,et al.  The Escherichia coli rep Gene , 1978 .

[13]  F. Foury,et al.  PIF1: a DNA helicase in yeast mitochondria. , 1991, The EMBO journal.

[14]  F. Foury,et al.  A PIF‐dependent recombinogenic signal in the mitochondrial DNA of yeast , 1985, The EMBO journal.

[15]  K. Bjornson,et al.  Mechanisms of helicase-catalyzed DNA unwinding. , 1996, Annual review of biochemistry.

[16]  B. Haarer,et al.  Immunofluorescence methods for yeast. , 1991, Methods in enzymology.

[17]  P. Perlman,et al.  Functions of the high mobility group protein, Abf2p, in mitochondrial DNA segregation, recombination and copy number in Saccharomyces cerevisiae. , 1998, Genetics.

[18]  G. Heijne Mitochondrial targeting sequences may form amphiphilic helices. , 1986 .

[19]  G. Bernardi,et al.  Replication origins are associated with transcription initiation sequences in the mitochondrial genome of yeast. , 1982, The EMBO journal.

[20]  U. Stahl,et al.  The protein family of RNA helicases. , 1998, Critical reviews in biochemistry and molecular biology.

[21]  F. Foury,et al.  pif mutation blocks recombination between mitochondrial rho+ and rho- genomes having tandemly arrayed repeat units in Saccharomyces cerevisiae. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[22]  W. Hauswirth,et al.  DNA helicase from mammalian mitochondria. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[23]  W. Neupert,et al.  The DNA Helicase, Hmi1p, Is Transported into Mitochondria by a C-terminal Cleavable Targeting Signal* , 1999, The Journal of Biological Chemistry.

[24]  A. Sancar DNA excision repair. , 1996, Annual review of biochemistry.

[25]  M. Costanzo,et al.  Analysis and manipulation of yeast mitochondrial genes. , 1991, Methods in enzymology.

[26]  J. Duffus,et al.  Yeast : a practical approach , 1988 .

[27]  P. Modrich,et al.  Mismatch repair, genetic stability, and cancer. , 1994, Science.

[28]  R. Sikorski,et al.  A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae. , 1989, Genetics.

[29]  M. Eilers,et al.  Import of proteins into mitochondria. , 1988, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[30]  F. Foury,et al.  Cloning and sequencing of the PIF gene involved in repair and recombination of yeast mitochondrial DNA. , 1987, The EMBO journal.

[31]  D. Grueneberg,et al.  Studying Heterologous Transcription Factors in Yeast , 1993 .

[32]  A. Myers,et al.  Mitochondrial protein synthesis is required for maintenance of intact mitochondrial genomes in Saccharomyces cerevisiae. , 1985, The EMBO journal.

[33]  G. Fink,et al.  Methods in yeast genetics , 1979 .

[34]  S. W. Matson,et al.  DNA helicases: Enzymes with essential roles in all aspects of DNA metabolism , 1994, BioEssays : news and reviews in molecular, cellular and developmental biology.

[35]  G. Daum,et al.  Import of proteins into mitochondria. Cytochrome b2 and cytochrome c peroxidase are located in the intermembrane space of yeast mitochondria. , 1982, The Journal of biological chemistry.

[36]  K. Köhrer,et al.  Preparation of high molecular weight RNA. , 1991, Methods in enzymology.

[37]  G. von Heijne Mitochondrial targeting sequences may form amphiphilic helices. , 1986, The EMBO journal.

[38]  W. L. Fangman,et al.  RPO41-independent maintenance of [rho-] mitochondrial DNA in Saccharomyces cerevisiae , 1990, Molecular and cellular biology.

[39]  R. Rothstein One-step gene disruption in yeast. , 1983, Methods in enzymology.