Abstract

Although the evolutionary importance of meiotic recombination is not disputed, the significance of interspecies differences in the recombination rates and recombination landscapes remains under-appreciated. Recombination rates and distribution of chiasmata have been examined cytologically in many mammalian species, whereas data on other vertebrates are scarce. Immunolocalization of the protein of the synaptonemal complex (SYCP3), centromere proteins and the mismatch-repair protein MLH1 was used, which is associated with the most common type of recombination nodules, to analyze the pattern of meiotic recombination in the male of two species of iguanian lizards, Anolis carolinensis Voigt, 1832 and Deiroptyx coelestinus (Cope, 1862). These species are separated by a relatively long evolutionary history although they retain the ancestral iguanian karyotype. In both species similar and extremely uneven distributions of MLH1 foci along the macrochromosome bivalents were detected: approximately 90% of crossovers were located at the distal 20% of the chromosome arm length. Almost total suppression of recombination in the intermediate and proximal regions of the chromosome arms contradicts the hypothesis that “homogenous recombination” is responsible for the low variation in GC content across the anole genome. It also leads to strong linkage disequilibrium between the genes located in these regions, which may benefit conservation of co-adaptive gene arrays responsible for the ecological adaptations of the anoles.

Highlights

  • IntroductionMeiotic recombination (crossing over) plays a dual role in sexually reproducing organisms

  • Meiotic recombination plays a dual role in sexually reproducing organisms

  • We examined the number and distribution of crossovers along their macrochromosomes using immunofluorescent localization of MLH1 at synaptonemal complexes (SCs) spreads

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Summary

Introduction

Meiotic recombination (crossing over) plays a dual role in sexually reproducing organisms. Crossing over shuffles allele combinations between homologous chromosomes, increasing the genetic variation in the progeny, on the one hand, and shaping local patterns of GCcontent (i.e., creating or modifying isochores) along the chromosome length, on the other hand (Eyre-Walker and Hurst 2001). The number and distribution of the crossovers along a chromosome depends on its length, chromatin composition, genetic content and crossover interference (Lynn et al 2002, Pardo-Manuel de Villena and Sapienza 2001). The occurrence of a crossover usually reduces the probability of another crossover close by. This phenomenon, which is called crossover interference, makes a substantial contribution to the number and distribution of crossovers along the chromosome (Moens 2006)

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