Assessment of phylogenetic approaches to study the timing of recombination cessation on sex chromosomes

Research output: Contribution to journalArticlepeer-review

Abstract

The evolution of sex chromosomes is hypothesized to be punctuated by consecutive recombination cessation events, forming “evolutionary strata” that ceased to recombine at different time points. The demarcation of evolutionary strata is often assessed by estimates of the timing of recombination cessation (tRC) along the sex chromosomes, commonly inferred from the level of synonymous divergence or with species phylogenies at gametologous (X-Y or Z-W) sequence data. However, drift and selection affect sequences unpredictably and introduce uncertainty when inferring tRC. Here, we assess two alternative phylogenetic approaches to estimate tRC; (i) the expected likelihood weight (ELW) approach that finds the most likely topology among a set of hypothetical topologies and (ii) the BEAST approach that estimates tRC with specified calibration priors on a reference species topology. By using Z and W gametologs of an old and a young evolutionary stratum on the neo-sex chromosome of Sylvioidea songbirds, we show that the ELW and BEAST approaches yield similar tRC estimates, and that both outperform two frequently applied approaches utilizing synonymous substitution rates (dS) and maximum likelihood (ML) trees, respectively. Moreover, we demonstrate that both ELW and BEAST provide more precise tRC estimates when sequences of multiple species are included in the analyses.

Original languageEnglish
Pages (from-to)1721-1733
JournalJournal of evolutionary biology
Volume35
Issue number12
Early online date2022
DOIs
Publication statusPublished - 2022

Subject classification (UKÄ)

  • Biological Systematics

Free keywords

  • evolutionary strata
  • phylogenetic approaches
  • sex chromosome
  • timing of recombination cessation

Fingerprint

Dive into the research topics of 'Assessment of phylogenetic approaches to study the timing of recombination cessation on sex chromosomes'. Together they form a unique fingerprint.

Cite this