Abstract

Numerous ancient whole-genome duplications (WGD) have occurred during eukaryote evolution. In vertebrates, duplicated developmental genes and their functional divergence have had important consequences for morphological evolution. Although two vertebrate WGD events (1R/2R) occurred over 525 Ma, we have focused on the more recent 3R or TGD (teleost genome duplication) event which occurred approximately 350 Ma in a common ancestor of over 26,000 species of teleost fishes. Through a combination of whole genome and bacterial artificial chromosome clone sequencing we characterized all Hox gene clusters of Pantodon buchholzi, a member of the early branching teleost subdivision Osteoglossomorpha. We find 45 Hox genes organized in only five clusters indicating that Pantodon has suffered more Hox cluster loss than other known species. Despite strong evidence for homology of the five Pantodon clusters to the four canonical pre-TGD vertebrate clusters (one HoxA, two HoxB, one HoxC, and one HoxD), we were unable to confidently resolve 1:1 orthology relationships between four of the Pantodon clusters and the eight post-TGD clusters of other teleosts. Phylogenetic analysis revealed that many Pantodon genes segregate outside the conventional “a” and “b” post-TGD orthology groups, that extensive topological incongruence exists between genes physically linked on a single cluster, and that signal divergence causes ambivalence in assigning 1:1 orthology in concatenated Hox cluster analyses. Out of several possible explanations for this phenomenon we favor a model which keeps with the prevailing view of a single TGD prior to teleost radiation, but which also considers the timing of diploidization after duplication, relative to speciation events. We suggest that although the duplicated hoxa clusters diploidized prior to divergence of osteoglossomorphs, the duplicated hoxb, hoxc, and hoxd clusters concluded diploidization independently in osteoglossomorphs and other teleosts. We use the term “tetralogy” to describe the homology relationship which exists between duplicated sequences which originate through a shared WGD, but which diploidize into distinct paralogs from a common allelic pool independently in two lineages following speciation.

Highlights

  • The vast majority of protein-coding genes can be organized into multigene families whose history has been shaped by duplication, loss, and speciation events (Dayhoff 1976; Nei and Rooney 2005; Demuth and Hahn 2009)

  • We have demonstrated that the Hox gene clusters of P. buchholzi represent a unique departure from the situation seen in other teleost fishes

  • We observe that phylogenetic analysis of the Hox clusters of P. buchholzi fails to support a shared TGD hypothesis unless a model accounting for diploidization after duplication is considered

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Summary

Introduction

The vast majority of protein-coding genes can be organized into multigene families whose history has been shaped by duplication, loss, and speciation events (Dayhoff 1976; Nei and Rooney 2005; Demuth and Hahn 2009). When comparing genes between species, sequences are classified by categories of molecular sequence homology first introduced by Fitch (1970) over 40 years ago: Orthology (the relationship between genes present in a common ancestor and separated through a speciation event) or paralogy (the relationship between sister genes generated through a gene duplication event). With the explosion in the availability of genome sequence data, largely facilitated by the advent of “Next-Generation” sequencing technologies (Metzker 2009), the importance of accurate homology assessment has grown. This is especially true in lineages where whole-genome duplication (WGD) has occurred, resulting in the simultaneous duplication of all genes

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