DNA Recombination-Initiation Plays a Role in the Extremely Biased Inheritance of Yeast [ rho − ] Mitochondrial DNA That Contains the Replication Origin ori5

Abstract

ABSTRACT Hypersuppressiveness, as observed in Saccharomyces cerevisiae , is an extremely biased inheritance of a small mitochondrial DNA (mtDNA) fragment that contains a replication origin (HS [ rho − ] mtDNA). Our previous studies showed that concatemers (linear head-to-tail multimers) are obligatory intermediates for mtDNA partitioning and are primarily formed by rolling-circle replication mediated by Mhr1, a protein required for homologous mtDNA recombination. In this study, we found that Mhr1 is required for the hypersuppressiveness of HS [ ori5 ] [ rho − ] mtDNA harboring ori5 , one of the replication origins of normal ([ rho + ]) mtDNA. In addition, we detected an Ntg1-stimulated double-strand break at the ori5 locus. Purified Ntg1, a base excision repair enzyme, introduced a double-stranded break by itself into HS [ ori5 ] [ rho − ] mtDNA at ori5 isolated from yeast cells. Both hypersuppressiveness and concatemer formation of HS [ ori5 ] [ rho − ] mtDNA are simultaneously suppressed by the ntg1 null mutation. These results support a model in which, like homologous recombination, rolling-circle HS [ ori5 ] [ rho − ] mtDNA replication is initiated by double-stranded breakage in ori5 , followed by Mhr1-mediated homologous pairing of the processed nascent DNA ends with circular mtDNA. The hypersuppressiveness of HS [ ori5 ] [ rho − ] mtDNA depends on a replication advantage furnished by the higher density of ori5 sequences and on a segregation advantage furnished by the higher genome copy number on transmitted concatemers.