Abstract

BackgroundMitochondria contain small genomes that are physically separate from those of nuclei. Their comparison serves as a model system for understanding the processes of genome evolution. Although complete mitochondrial genome sequences have been reported for more than 600 animals, the taxonomic sampling is highly biased toward vertebrates and arthropods, leaving much of the diversity yet uncharacterized.ResultsThe mitochondrial genome of the bellybutton nautilus, Nautilus macromphalus, a cephalopod mollusk, is 16,258 nts in length and 59.5% A+T, both values that are typical of animal mitochondrial genomes. It contains the 37 genes that are almost universally found in animal mtDNAs, with 15 on one DNA strand and 22 on the other. The arrangement of these genes can be derived from that of the distantly related Katharina tunicata (Mollusca: Polyplacophora) by a switch in position of two large blocks of genes and transpositions of four tRNA genes. There is strong skew in the distribution of nucleotides between the two strands, and analysis of this yields insight into modes of transcription and replication. There is an unusual number of non-coding regions and their function, if any, is not known; however, several of these demark abrupt shifts in nucleotide skew, and there are several identical sequence elements at these junctions, suggesting that they may play roles in transcription and/or replication. One of the non-coding regions contains multiple repeats of a tRNA-like sequence. Some of the tRNA genes appear to overlap on the same strand, but this could be resolved if the polycistron were cleaved at the beginning of the downstream gene, followed by polyadenylation of the product of the upstream gene to form a fully paired structure.ConclusionNautilus macromphalus mtDNA contains an expected gene content that has experienced few rearrangements since the evolutionary split between cephalopods and polyplacophorans. It contains an unusual number of non-coding regions, especially considering that these otherwise often are generated by the same processes that produce gene rearrangements. The skew in nucleotide composition between the two strands is strong and associated with the direction of transcription in various parts of the genomes, but a comparison with K. tunicata implies that mutational bias during replication also plays a role. This appears to be yet another case where polyadenylation of mitochondrial tRNAs restores what would otherwise be an incomplete structure.

Highlights

  • Mitochondria contain small genomes that are physically separate from those of nuclei

  • The Nautilus macromphalus mitochondrial genome is 16,258 bp in length (GenBank accession number DQ472026) and contains the set of 37 genes most commonly found for animal mitochondrial DNA (mtDNA) [5]

  • In order to determine which of these differences were caused by changes in the lineage leading to Polyphacophora versus those leading to the cephalopods, it is useful to identify more distantly related animals that share one or the other arrangement; since it seems very unlikely that identical rearrangements would occur in different lineages, one can reasonably infer that any gene arrangement shared by this outgroup taxon with either the polyplacophoran or a cephalopod is the ancestral condition for the common ancestor of the latter two groups

Read more

Summary

Introduction

Mitochondria contain small genomes that are physically separate from those of nuclei Their comparison serves as a model system for understanding the processes of genome evolution. [1,2,3,4]], contains the same 37 genes, specifying 13 proteins, two ribosomal RNAs, and 22 tRNAs [5]. Sequences of these diminutive genomes have been broadly used to address phylogenetic questions ranging from the population [6,7] to the interphylum [8,9,10,11] levels and to model many processes of genome evolution [12,13]. Post-transcriptional modification of nucleotides has been observed for tRNAs [21,22]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call