Abstract
Simple SummaryChromosome rearrangements are one of the main etiological factors leading to impaired fertility in the domestic pig. The high prevalence of chromosome rearrangements in swine herds, coupled with the production of significantly lower litter sizes, has led to the implementation of cytogenetics techniques in screening prospective breeding boars for rearrangements. Beginning in the 1960s, classical cytogenetics techniques have been applied in laboratories, resulting in the identification of over 200 distinct chromosome rearrangements in the pig. More recently advances in technology, and the development of molecular cytogenetics and cytogenomics techniques, have enhanced the resolution of rearrangements and advanced diagnostic techniques, allowing for more precise and rapid diagnosis of rearrangements.The chromosomes of the domestic pig (Sus scrofa domesticus) are known to be prone to reciprocal chromosome translocations and other balanced chromosome rearrangements with concomitant fertility impairment of carriers. In response to the remarkable prevalence of chromosome rearrangements in swine herds, clinical cytogenetics laboratories have been established in several countries in order to screen young boars for chromosome rearrangements prior to service. At present, clinical cytogenetics laboratories typically apply classical cytogenetics techniques such as giemsa-trypsin (GTG)-banding to produce high-quality karyotypes and reveal large-scale chromosome ectopic exchanges. Further refinements to clinical cytogenetics practices have led to the implementation of molecular cytogenetics techniques such as fluorescent in-situ hybridization (FISH), allowing for rearrangements to be visualized and breakpoints refined using fluorescently labelled painting probes. The next-generation of clinical cytogenetics include the implementation of DNA microarrays, and next-generation sequencing (NGS) technologies such as DNA sequencing to better explore tentative genome architecture changes. The implementation of these cytogenomics techniques allow the genomes of rearrangement carriers to be deciphered at the highest resolution, allowing rearrangements to be detected; breakpoints to be delineated; and, most importantly, potential gene implications of those chromosome rearrangements to be interrogated. Clinical cytogenetics has become an integral tool in the livestock industry, identifying rearrangements and allowing breeders to make informed breeding decisions.
Highlights
The domestic pig (Sus scrofa domesticus) is known to have a high proportion of chromosomal rearrangements relative to other species [1]
primed in-situ labelling (PRINS) is used as an alternative technique to fluorescent in-situ hybridization (FISH), for similar applications in the observation of chromosome rearrangements, and gene loci, with the focus on rearrangements located near repetitive sequences in the genome [102]
Cytogenomics, which refers to the use of DNA microarrays and whole genome sequencing (WGS) tools to visualize the genome at a high resolution, has increased in prominence
Summary
The domestic pig (Sus scrofa domesticus) is known to have a high proportion of chromosomal rearrangements relative to other species [1]. Screening programs cannot totally eliminate rearrangements from herds, they can prevent carriers from breeding, resulting in the maintenance of litter size, eliminating the possibility of inheritance, and reducing the prevalence of rearrangements. In countries where such programs are available, many breeders will voluntarily submit their breeding boars for cytogenetic screening, seeing clear economic benefits to managing the presence of rearrangements [7]. Though relatively sparse and underutilized, serve an important purpose to identify chromosomal rearrangements and other chromosome abnormalities in the pig genome, to assist selection of boars for breeding services and to help further the study and understanding of chromosome rearrangements in the domestic pig, including their breadth, diagnosis, origins, and the effect they have on meiosis and the genome itself
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