Abstract

Chromosome number change (polyploidy and dysploidy) plays an important role in plant diversification and speciation. Investigating chromosome number evolution commonly entails ancestral state reconstruction performed within a phylogenetic framework, which is, however, prone to uncertainty, whose effects on evolutionary inferences are insufficiently understood. Using the chromosomally diverse plant genus Melampodium (Asteraceae) as model group, we assess the impact of reconstruction method (maximum parsimony, maximum likelihood, Bayesian methods), branch length model (phylograms versus chronograms) and phylogenetic uncertainty (topological and branch length uncertainty) on the inference of chromosome number evolution. We also address the suitability of the maximum clade credibility (MCC) tree as single representative topology for chromosome number reconstruction. Each of the listed factors causes considerable incongruence among chromosome number reconstructions. Discrepancies between inferences on the MCC tree from those made by integrating over a set of trees are moderate for ancestral chromosome numbers, but severe for the difference of chromosome gains and losses, a measure of the directionality of dysploidy. Therefore, reliance on single trees, such as the MCC tree, is strongly discouraged and model averaging, taking both phylogenetic and model uncertainty into account, is recommended. For studying chromosome number evolution, dedicated models implemented in the program ChromEvol and ordered maximum parsimony may be most appropriate. Chromosome number evolution in Melampodium follows a pattern of bidirectional dysploidy (starting from x = 11 to x = 9 and x = 14, respectively) with no prevailing direction.

Highlights

  • Chromosome number change plays an important role in eukaryotic evolution in general and in plant diversification and speciation in particular [1, 2]

  • We address the suitability of the maximum clade credibility (MCC) tree as single representative topology for chromosome number reconstruction

  • Variances of gains minus chromosome losses (G-L) distributions were smallest in the Maximum Parsimony (MP) analysis, largest in the Bayesian analysis (BI) analysis, and intermediate in the Maximum Likelihood (ML)-CE and models tested in BAYESTRAITS (ML-BT) analyses

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Summary

Introduction

Chromosome number change plays an important role in eukaryotic evolution in general and in plant diversification and speciation in particular [1, 2]. Dysploidy is the homoploid change of the chromosome base number via chromosomal rearrangements without significant loss of genetic material [3]. Polyploidy is the multiplication of entire chromosome sets. It has become a major focus in plant evolutionary biology due to the recognition of the ubiquity of polyploidy in angiosperms via identification of several rounds of whole genome duplication affecting even small angiosperm genomes [9, 10]. Aneuploidy refers to the loss or gain of entire chromosomes and of genetic material, which is rarely tolerated by plants [3]. Like the presence of accessory chromosomes (B-chromosomes), aneuploidy is usually transitory and plays only a minor role in evolutionary terms [1]

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