Abstract

The relative female and male contributions to demography are of great importance to better understand the history and dynamics of populations. While earlier studies relied on uniparental markers to investigate sex-specific questions, the increasing amount of sequence data now enables us to take advantage of tens to hundreds of thousands of independent loci from autosomes and the X chromosome. Here, we develop a novel method to estimate effective sex ratios or ESR (defined as the female proportion of the effective population) from allele count data for each branch of a rooted tree topology that summarizes the history of the populations of interest. Our method relies on Kimura’s time-dependent diffusion approximation for genetic drift, and is based on a hierarchical Bayesian model to integrate over the allele frequencies along the branches. We show via simulations that parameters are inferred robustly, even under scenarios that violate some of the model assumptions. Analyzing bovine SNP data, we infer a strongly female-biased ESR in both dairy and beef cattle, as expected from the underlying breeding scheme. Conversely, we observe a strongly male-biased ESR in early domestication times, consistent with an easier taming and management of cows, and/or introgression from wild auroch males, that would both cause a relative increase in male effective population size. In humans, analyzing a subsample of non-African populations, we find a male-biased ESR in Oceanians that may reflect complex marriage patterns in Aboriginal Australians. Because our approach relies on allele count data, it may be applied on a wide range of species.

Highlights

  • In dioecious species, contrasting patterns of genetic differentiation between males and females provide important information on social organization [1], dispersal and mating patterns [2, 3], and demographic history [4]

  • Estimation of the female proportion of the effective population is important to better understand this underlying social structure and dynamics. This question has been mainly investigated so far by comparing genetic variation of mitochondrial DNA and the Y chromosome, two uniparentally inherited markers that reflect the demographic history of females and males, respectively

  • The characterization of sex-specific genetic variation has mainly been based on uniparentally inherited markers: mitochondrial DNA, which is transmitted by females to their offspring, and the non-recombining portion of the Y chromosome (NRY), which is inherited through the male line only [8,9,10,11,12,13,14]

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Summary

Introduction

In dioecious species, contrasting patterns of genetic differentiation between males and females provide important information on social organization [1], dispersal and mating patterns [2, 3], and demographic history [4]. Due to the lack of recombination in both mtDNA and NRY, the potential influence of other evolutionary forces, in particular selection, challenge the interpretation of the observed patterns of genetic diversity [15,16,17]. To circumvent this problem, an alternative approach has been proposed, which consists in comparing the amount of genetic variation at both autosomal and X-linked markers [18]. Such markers are highly informative about demographic differences between males and females [15], as was shown from the inference of sex-specific processes from the analysis of microsatellite markers [1, 3, 18], single nucleotide polymorphisms (SNPs) [19,20,21] and sequence data [22, 23]

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