Abstract

Hybrid sterility is an important step in the speciation process. Hybrids between dwarf hamsters Phodopus sungorus and P. campbelli provide a good model for studies in cytological and genetic mechanisms of hybrid sterility. Previous studies in hybrids detected multiple abnormalities of spermatogenesis and a high frequency of dissociation between the X and Y chromosomes at the meiotic prophase. In this study, we found that the autosomes of the hybrid males and females underwent paring and recombination as normally as their parental forms did. The male hybrids showed a significantly higher frequency of asynapsis and recombination failure between the heterochromatic arms of the X and Y chromosomes than the males of the parental species. Female hybrids as well as the females of the parental species demonstrated a high incidence of centromere misalignment at the XX bivalent and partial asynapsis of the ends of its heterochromatic arms. In all three karyotypes, recombination was completely suppressed in the heterochromatic arm of the X chromosome, where the pseudoautosomal region is located. We propose that this recombination pattern speeds up divergence of the X- and Y-linked pseudoautosomal regions between the parental species and results in their incompatibility in the male hybrids.

Highlights

  • Accumulation of genetic differences during an independent evolution of geographically isolated populations leads to incompatibility between parental genomes

  • The average testis mass was significantly lower in the hybrids (0.255 ± 0.182 g) compared to P. sungorus (0.727 ± 0.024 g) and P. campbelli (1.158 ± 0.021 g) (Mann–Whitney U test, p < 0.01)

  • Our histological data confirmed the complete sterility of F1 male hybrids between P. sungorus and P. campbelli detected in previous studies [11,18,19]

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Summary

Introduction

Accumulation of genetic differences during an independent evolution of geographically isolated populations leads to incompatibility between parental genomes. Hybrid sterility is the most common symptom of such incompatibility. Studies on mammalian hybrids indicated abnormalities in meiotic chromosome pairing as a common cause of hybrid sterility [3,4,5,6]. They confirmed the validity of Haldane’s rule stating that signs of sterility occur earlier and are stronger in hybrids of the heterogametic sex than in the homogametic sex [7]. Male hybrid sterility is often accompanied by pairing and recombination failure in the pseudoautosomal region (PAR), a short genome region retaining homology between the X and Y chromosomes [8,9,10,11,12]

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