Abstract

Whole genome assemblies are crucial for understanding a wide range of aspects of falcon biology, including morphology, ecology, and physiology, and are thus essential for their care and conservation. A key aspect of the genome of any species is its karyotype, which can then be linked to the whole genome sequence to generate a so-called chromosome-level assembly. Chromosome-level assemblies are essential for marker assisted selection and genotype-phenotype correlations in breeding regimes, as well as determining patterns of gross genomic evolution. To date, only two falcon species have been sequenced and neither initially were assembled to the chromosome level. Falcons have atypical avian karyotypes with fewer chromosomes than other birds, presumably brought about by wholesale fusion. To date, however, published chromosome preparations are of poor quality, few chromosomes have been distinguished and standard ideograms have not been made. The purposes of this study were to generate analyzable karyotypes and ideograms of peregrine, saker, and gyr falcons, report on our recent generation of chromosome level sequence assemblies of peregrine and saker falcons, and for the first time, sequence the gyr falcon genome. Finally, we aimed to generate comparative genomic data between all three species and the reference chicken genome. Results revealed a diploid number of 2n = 50 for peregrine falcon and 2n = 52 for saker and gyr through high quality banded chromosomes. Standard ideograms that are generated here helped to map predicted chromosomal fragments (PCFs) from the genome sequences directly to chromosomes and thus generate chromosome level sequence assemblies for peregrine and saker falcons. Whole genome sequencing was successful in gyr falcon, but read depth and coverage was not sufficient to generate a chromosome level assembly. Nonetheless, comparative genomics revealed no differences in genome organization between gyr and saker falcons. When compared to peregrine falcon, saker/gyr differed by one interchromosomal and seven intrachromosomal rearrangements (a fusion plus seven inversions), whereas peregrine and saker/gyr differ from the reference chicken genome by 14/13 fusions (11 microchromosomal) and six fissions. The chromosomal differences between the species could potentially provide the basis of a screening test for hybrid animals.

Highlights

  • Study of the genomics of falcon species is important for understanding a wide range of aspects of falcon biology, including morphology, ecology, and physiology, as well as being essential for conservation efforts

  • Chromosomes 17–25 are generally indistinguishable microchromosomes with the exception of chromosome 25, which is much brighter under propidium iodide

  • F. peregrinus is similar, with the two fused chromosomes making up chromosome 1 and the inversions taken into account

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Summary

Introduction

Study of the genomics of falcon species is important for understanding a wide range of aspects of falcon biology, including morphology, ecology, and physiology, as well as being essential for conservation efforts. In addition to the sequence itself, a key aspect of the genomics of any species is its karyotype [3]. The ultimate aim of any de novo genome sequencing effort is to assign all or most of the sequences to the appropriate chromosomes in the karyotype, with each gene or marker in order–in essence, creating a genomic map [4]. Making a map of the genome in relation to the karyotype (a so-called chromosome-level assembly) can be useful for genotype-phenotype correlations, followed by marker assisted selection in breeding regimes [5]

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