14 - What can the Mus musculus musculus/M. m. domesticus hybrid zone tell us about speciation?  pp. 334-372

What can the <i>Mus musculus musculus/M. m. domesticus</i> hybrid zone tell us about speciation?

By Stuart J. E. Baird and Miloš Macholán

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Introduction

One of the crucial tasks in the study of speciation is to explain the genetic basis of reproductive barriers between diverged taxa. Despite the best endeavours of generations of evolutionary biologists since Darwin and Wallace, our understanding of the genetics of speciation has lagged behind other fields of evolutionary biology. The reason may be simply that the greater the reproductive isolation, the less cross progeny we have to work with, but more probably it is because the genetic factors involved are numerous, with complex interactions. Indeed, it appears that except for a few cases (Coyne and Orr, 2004) reproductive isolation arises in many small steps rather than a few strongly selected mutations, in agreement with theoretical predictions (Walsh, 1982; Barton and Charlesworth, 1984). Obviously, the more genes with small effect that are involved in reproductive isolation, the more difficult will be their identification, making traditional laboratory hybridization experiments and association studies challenging.

It seems only common sense, therefore, to search for alternative approaches. One promising alternative is to study naturally occurring hybrid zones. The seeds for progress were sown by Barton and Hewitt (1985, 1989), who suggested the majority of hybrid zones were ‘tension zones’ (Box 14.1). While initially received with scepticism in some quarters, the tension zone paradigm now dominates the hybrid zone literature and is arguably the main justification for the view that hybrid zones are ‘natural laboratories’ (Hewitt, 1988) and ‘windows on evolutionary process’ (Harrison, 1990). The reason this paradigm is so important is that it unifies hybrid zone process over a diversity of species, geographic scales, and histories of contact into a single analytically tractable framework (Box 14.2) with intuitive, testable results and predictions that have been borne out repeatedly over the subsequent decades. Tension zones are measured relative to the scale of dispersal of the organism involved, and on this metric the stronger the selection against admixture the more abrupt are the changes between the taxa (clines) we see as we cross the hybrid zone. This simple contrast (strong selection = narrow cline; weak selection = wide cline) holds even when comparing snail hybrid zones to bird hybrid zones – as long as we measure width relative to their respective dispersal scales – but comparisons across clines at loci within the same genome are even more robust.

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