Abstract

Mitochondrial DNA (mtDNA) and Y chromosome (NRY) genetic markers have been often contrasted to investigate sex-specific dynamics. Traditionally, isolation by distance, intrapopulation genetic diversity and population differentiation are estimated from both markers and compared. Two possible sources of bias are often neglected. First, kilometric distances are frequently used as predictor of the connectivity between groups, hiding the role played by environmental features at a microgeographic scale. Second, the comparison of intrapopulation diversity and population differentiation between mtDNA and NRY is hampered by their different mutational mechanisms and rates. Here, we show how to account for these biases by analyzing from a different perspective a published dataset of eight West New Guinea (WNG) populations for which mtDNA control region sequences and seven linked NRY microsatellites had been typed. First, we modeled the connectivity among sampled populations by computing the number of days required to travel between groups. Then, we investigated the differences between the two sexes accounting for the molecular characteristics of the markers examined to obtain estimates on the product of the effective population size and the migration rate among demes (Nm). We achieved this goal by studying the shape of the gene genealogy at several sampling levels and using spatial explicit simulations. Both the direction and the rate of migration differ between male and females, with an Nm estimated to be >6 times higher in the latter under many evolutionary scenarios. We finally highlight the importance of applying metapopulation models when analyzing the genetic diversity of a species.We have applied the prediction of the sampling theory in a meta-population and we have corroborated our finding using spatial explicit simulations. Both approaches are fundamentally meant to deal with structured populations: we strongly believe in the importance of tacking structure into account when inferring the demographic history of a species.

Highlights

  • Sex-specific demographic patterns are traditionally investigated in humans by using uniparentally inherited markers, namely mitochondrial DNA for females and Y chromosome (NRY) for males

  • Ecology and Evolution published by John Wiley & Sons Ltd

  • Uniparental markers, namely mitochondrial DNA (mtDNA) and NRY, have been used for a long time to characterize the influence of sex-specific behaviors on the genetic structure and diversity of human populations (Heyer et al 2012)

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Summary

Introduction

Sex-specific demographic patterns are traditionally investigated in humans by using uniparentally inherited markers, namely mitochondrial DNA (mtDNA) for females and Y chromosome (NRY) for males. Different conclusions have been drawn depending on the region investigated (Seielstad et al 1998; Oota et al 2001; Fuselli et al 2003; Kayser et al 2003; Nasidze et al 2004; Kemp et al 2012), on the geographic scale of the study (Wilder et al 2004; Wilkins and Marlowe 2006) and on the specific locus ascertained on both mtDNA and NRY (Wilder et al 2004; Gunnarsdottir et al 2012).

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