Hello all.
Yes there was not a whole lot of "talk" after my report. There was quite an excited response at the meeting, but since I was on the phone, I coundnt tell much. I dont think the vast majority realized what I have finally accomplished. Below is the first abstract of my research to be presented at ESS (Equine Science Society) in May 29-31. This will be refined and expanded with my latest results this week (since the AMHA meeting). I have found the mutation and I am currently designing a test.
Once this work is finished this spring, I will hope to have it accepted to a genetics journal for print.
THere will be other papers along with this one that characterize the phenotypes of dwarfisms in the Miniatures with pathological examinations and characterizations. I hope to work on the other types as well to find those mutations on the side while I work on my PhD thesis, which is not on dwarfism. It is on an inherited reproductive abnormality in all horses.
Investigation of Dwarfism Among Miniature Horses using the Illumina Horse SNP50 Bead Chip.
J. Eberth*, T. Swerczak, E. Bailey; MH Gluck Equine Research Center/ University of Kentucky, Lexington, KY, USA
Introduction
Ponies and Miniature horses differ from full size horse only by their stature. Ponies are often defined as those whose height is not greater than 14.2 hands, however the maximum height for Miniature horses is constitutionally defined as 8.2 hands. This reduced stature is usually the cumulative effect of hundreds of genes, each having a small impact on stature. Unfortunately, there are also dwarfism genes which greatly reduce statute and may negatively impact health and reproduction. This is not considered a desirable genetic trait for Miniature horses. Therefore, the following studies were conducted to discover the genetic basis for dwarfism.
Materials and Methods
Pedigree records suggested that dwarfism occurs as a recessive genetic trait among miniature horses. Pathological examination, involving comparison of skeletal development and other phenotypic traits, suggested that there may be as many as four distinct types of dwarfism segregating among miniature horses. Indeed, among humans there are over 100 genetic mutations found responsible for different forms of dwarfism.
Type I dwarves exhibit cranial abnormalities of a disproportionately large head, large bulging eyes and eye sockets, a forehead with relative frontal domed prominence and a relatively short stubbed muzzle. An underbite of variable severity is commonly seen in this type however some have a normal bite. The midface is often small with a flat nasal bridge and narrow nasal passages and the airway obstruction can be "central" in origin (due to foramen magnum compression) or "obstructive" in origin (due to narrowed nasal passages). Symptoms of airway obstruction include snoring. Other characteristics are shortened limbs, enlarged joints, malformed or bowed legs with limited extension and flexion and overall disproportionate short stature. Progressive hoof deformities resulting from malformed limbs as well as progressive arthritis in the limbs become worse with age. Spinal abnormalities such as roachback may or may not develop later.
To avoid pooling samples from different genetic forms of dwarfism, horses were selected based on a common phenotype and belonging to a common family line. This phenotype was identified as Type I dwarfism of miniature horses. DNA was isolated from blood or tissues of 20 horses exhibiting type I dwarfism and from 20 relatives that did not exhibit the dwarfism traits. The DNA was tested using the Illumina Equine SNP50 bead chip. The results were analyzed using PLINK v 1.04.
Results
A single chromosome region was strongly associated with the trait. EMP2 (empirical P value, corrected for all tests) value of 0.019 was obtained, strongly supporting this candidate region. Within the candidate region a candidate gene was found which causes dwarfism among humans.
Discussion
The candidate gene is currently being sequenced for horses with the hope of discovering a mutation responsible for the trait. Additional work will entail identifying a haplotype signature for Type I dwarfism that could be used to estimate its frequency in the population and determine the phenotypic heterogeneity associated with this haplotype.
ACKNOWLEDGEMENTS
Morris Animal Foundation and the American Miniature Horse Association provided funds for this research.