Abstract

Genome size varies widely among organisms and is known to affect vertebrate development, morphology, and physiology. In amphibians, genome size is hypothesized to contribute to loss of late-forming structures, although this hypothesis has mainly been discussed in salamanders. Here we estimated genome size for 22 anuran species and combined this novel data set with existing genome size data for an additional 234 anuran species to determine whether larger genome size is associated with loss of a late-forming anuran sensory structure, the tympanic middle ear. We established that genome size is negatively correlated with development rate across 90 anuran species and found that genome size evolution is correlated with evolutionary loss of the middle ear bone (columella) among 241 species (224 eared and 17 earless). We further tested whether the development of the tympanic middle ear could be constrained by large cell sizes and small body sizes during key stages of tympanic middle ear development (metamorphosis). Together, our evidence suggests that larger genomes, slower development rate, and smaller body sizes at metamorphosis may contribute to the loss of the anuran tympanic middle ear. We conclude that increases in anuran genome size, although less drastic than those in salamanders, may affect development of late-forming traits.

Highlights

  • Genome size evolution alters development, morphology, and physiology across vertebrates

  • We estimated genome size for 22 anuran species and combined this novel data set with existing genome size data for an additional 234 anuran species to determine whether larger genome size is associated with loss of a late-forming anuran sensory structure, the tympanic middle ear

  • We established that genome size is negatively correlated with development rate across 90 anuran species and found that genome size evolution is correlated with evolutionary loss of the middle ear bone among 241 species (224 eared and 17 earless)

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Summary

Introduction

Genome size evolution alters development, morphology, and physiology across vertebrates. Larger cells take longer to proliferate (Shuter et al 1983; Vinogradov 1999), which is thought to contribute to slower embryonic development (Bachmann 1972; Oeldorf et al 1978; Horner and Macgregor 1983; Chipman et al 2001), larval development (Goin et al 1968; Camper et al 1993), and limb regeneration (Sessions and Larson 1987) in amphibians with larger genomes This slowing of development rate (neoteny) can lead to paedomorphosis, a form of heterochrony (change in developmental timing) in which organisms become sexually mature before all traits have reached their adult phenotype (Wake 1966; Gould 1977; Alberch et al 1979; McNamara 1986). The relationship between larger genome size and evolutionary lability of late-forming traits has limited empirical support

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