Abstract

Postzygotic reproductive isolation is characterized by two striking empirical patterns. The first is Haldane's rule—the preferential inviability or sterility of species hybrids of the heterogametic (XY) sex. The second is the so-called large X effect—substitution of one species's X chromosome for another's has a disproportionately large effect on hybrid fitness compared to similar substitution of an autosome. Although the first rule has been well-established, the second rule remains controversial. Here, we dissect the genetic causes of these two rules using a genome-wide introgression analysis of Drosophila mauritiana chromosome segments in an otherwise D. sechellia genetic background. We find that recessive hybrid incompatibilities outnumber dominant ones and that hybrid male steriles outnumber all other types of incompatibility, consistent with the dominance and faster-male theories of Haldane's rule, respectively. We also find that, although X-linked and autosomal introgressions are of similar size, most X-linked introgressions cause hybrid male sterility (60%) whereas few autosomal introgressions do (18%). Our results thus confirm the large X effect and identify its proximate cause: incompatibilities causing hybrid male sterility have a higher density on the X chromosome than on the autosomes. We evaluate several hypotheses for the evolutionary cause of this excess of X-linked hybrid male sterility.

Highlights

  • Speciation occurs when two populations become reproductively isolated from each other through the evolution of one or more barriers to gene flow [1,2]

  • The evolution of reproductive isolation is a fundamental step in the origin of species

  • We dissected the genetic causes of these two rules of speciation by replacing many small chromosomal segments of the fruit fly Drosophila sechellia with those of a closely related species, D. mauritiana

Read more

Summary

Introduction

Speciation occurs when two populations become reproductively isolated from each other through the evolution of one or more barriers to gene flow [1,2]. A model describing the evolution of hybrid inviability and hybrid sterility was proposed independently by Dobzhansky [1] and Muller [3] The essence of their idea is that divergence at interacting loci between species can cause deleterious, incompatible epistatic interactions in interspecific hybrids. Faster evolution of X-linked loci (the faster-X theory [35]; but see [36,37]) and some forms of genetic conflict [31,38,39,40,41,42], have been suggested as causes of Haldane’s rule, but their general importance remains unclear.

Author Summary
Findings
Materials and Methods
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call