Whole-chromosome fusions in the karyotype evolution of Sceloporus (Iguania, Reptilia) are more intense in sex chromosomes than autosomes
There is a growing body of evidence that the common ancestor of vertebrates had a bimodal karyotype, i.e. consisting of large macrochromosomes and small microchromosomes. This type of karyotype organization is preserved in most reptiles. However, certain species independently experience microchromosome fusions. The evolutionary forces behind this are unclear. We investigated the karyotype of the green spiny lizard, Sceloporus malachiticus, an iguana species which has 2n=22, whereas the ancestral karyotype of iguanas had 2n=36. We obtained and sequenced flow-sorted chromosome-specific DNA samples and found that most of the microchromosome fusions in this species involved sex chromosomes. We found that certain ancestral squamate chromosomes, such as the homologue of the Anolis carolinensis chromosome 11, are repeatedly involved in sex chromosome formation in different species. To test the hypothesis that the karyotypic shift could be associated with changes in recombination patterns, and to study sex chromosome synapsis and recombination in meiosis, we performed synaptonemal complex analysis in this species and in S. variabilis, a related species with 2n=34. We found that in the species studied the recombination patterns correlate more with phylogeny than with the structure of the karyotype. The sex chromosomes had two distal pseudoautosomal regions and a medial differentiated region.