James Cotton:

Abstract

An unusual genetic system has allowed recombination to be recognized in an animal mitochondrial genome. Significance and context Maternal transmission of mitochondria is the rule-of-thumb across all eukaryotes, but important exceptions have long been known. Plants, for example, show the whole range of mitochondrial inheritance, from fully maternal through biparental to paternal inheritance. Closer to home, paternal leakage has been reported in a fungus, in Drosophila and even in mice, and a particularly exotic pattern of inheritance has been demonstrated in mussels. The ruling paradigm of purely maternal inheritance came hand-in-hand with the assumption that mitochondrial DNA (mtDNA) did not recombine, but there is now direct evidence of homologous recombination in plant, fungus and protist mtDNA. The belief that animal mtDNA does not undergo homologous recombination has proved harder to shake. This is rather surprising, as this paradigm is based on indirect evidence and is challenged by a growing body of data. The original observation that paternal mitochondria do not penetrate the egg is now known to be in error, with paternal organelles persisting for several hours after fertilization. It is also known that mammalian mitochondria contain the necessary enzymatic machinery for homologous recombination, and mitochondrial fusion is well known in Drosophila. Non-homologous recombination (unequal crossing-over) has been held responsible for variation in the number of tandem repeats in a number of animal mitochondrial genomes, and has been directly observed in a nematode. Two recent population studies have also suggested that recombination has occurred in human mtDNA. With all this evidence, it would seem likely that homologous recombination does occur in animal mitochondria, but the publication of human population studies last year provoked considerable debate, emphasizing that there is much interest in whether animal mtDNA does show homologous recombination, and considerable skepticism. Many authors will no doubt remain skeptical, despite the results of this paper, in which Ladoukakis and Zouros have exploited the unusual genetic system of the mussel to uncover direct evidence for homologous recombination within animal mitochondria. The unusual biparental inheritance of mitochondria in mussels of the families Unionidea and Mytilidaehas been known for about a decade, and is an interesting exception to the otherwise universal rule of maternal inheritance for animal mtDNA. Normally, female (F) and male (M) mitochondrial sequences differ by 20% too great an amount to expect to observe homologous recombination. Luckily, a quirk of the Mytilus system allows a unique opportunity to observe mtDNA recombination in action. Occasionally, F genomes become 'masculinized', invading the M transmission route in sperm (see Figure 1). These MF genomes can now diverge from the ancestral F form, so we can find in a single cell mitochondrial genomes that have sufficient sequence difference to allow homologous recombination to be detected, but not so much that recombination would be suppressed. The authors report a number of sequences from the gene for cytochrome oxidase subunit III, where it seems clear that short pieces of DNA have been exchanged between F and MF mtDNA. Out of thirteen different sequences, six appear to be recombinants between the two most common alleles in the population, with recombinant fragments ranging in length from 24 bases to over 200. Figure 1 The unusual mitochondrial inheritance sy Key results Methodological innovations The molecular techniques used in this work are standard, but I was impressed by the thoroughness with which Ladoukakis and Zouros ensured that their results were due to genuine in vivo recombination and not to 'in vitro recombination' in the formation of PCR chimeras.