The mitochondrial nucleoid protein, Mgm101p, of Saccharomyces cerevisiae is involved in the maintenance of rho(+) and ori/rep-devoid petite genomes but is not required for hypersuppressive rho(-) mtDNA

Genetics. 2002 Apr;160(4):1389-400. doi: 10.1093/genetics/160.4.1389.

Abstract

The Saccharomyces cerevisiae MGM101 gene encodes a DNA-binding protein targeted to mitochondrial nucleoids. MGM101 is essential for maintenance of a functional rho(+) genome because meiotic segregants, with a disrupted mgm101 allele, cannot undergo more than 10 divisions on glycerol medium. Quantitative analysis of mtDNA copy number in a rho(+) strain carrying a temperature-sensitive allele, mgm101-1, revealed that the amount of mtDNA is halved each cell division upon a shift to the restrictive temperature. These data suggest that mtDNA replication is rapidly blocked in cells lacking MGM101. However, a small proportion of meiotic segregants, disrupted in MGM101, have rho(-) genomes that are stably maintained. Interestingly, all surviving rho(-) mtDNAs contain an ori/rep sequence. Disruption of MGM101 in hypersuppressive (HS) strains does not have a significant effect on the propagation of HS rho(-) mtDNA. However, in petites lacking an ori/rep, disruption of MGM101 leads to either a complete loss or a dramatically decreased stability of mtDNA. This discriminatory effect of MGM101 suggests that replication of rho(+) and ori/rep-devoid rho(-) mtDNAs is carried out by the same process. By contrast, the persistence of ori/rep-containing mtDNA in HS petites lacking MGM101 identifies a distinct replication pathway. The alternative mtDNA replication mechanism provided by ori/rep is independent of mitochondrial RNA polymerase encoded by RPO41 as a HS rho(-) genome is stably maintained in a mgm101, rpo41 double mutant.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Replication*
  • DNA, Mitochondrial / biosynthesis*
  • DNA-Binding Proteins
  • Fungal Proteins / physiology*
  • Hot Temperature
  • Mitochondria / genetics
  • Mitochondrial Proteins
  • Mutation
  • Nuclear Proteins / physiology*
  • Replication Origin
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae Proteins / physiology*

Substances

  • DNA, Mitochondrial
  • DNA-Binding Proteins
  • Fungal Proteins
  • MGM101 protein, S cerevisiae
  • Mitochondrial Proteins
  • Nuclear Proteins
  • Saccharomyces cerevisiae Proteins