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Osteochondrosis (OC) is a developmental orthopedic disorder in young, growing horses, where irregular bone formation in the joints leads to necrotic areas, resulting in chronic or recurrent lameness. Incidence of OC varies considerably among breeds, and displays a multifactorial mode of inheritance. The incidence of \(\mathrm{OC}\) is rising in the population of race horses. Discuss the reasons why the incidence of OC might be rising, and describe what can be done to detect OC susceptibility in horses with the help of QTL analysis.

Short Answer

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Answer: Possible reasons for the rising incidence of Osteochondrosis in racehorses may include selective breeding, increased stress on joints, and nutritional factors. QTL analysis can help detect OC susceptibility by collecting phenotypic and genotypic data, performing linkage analysis to identify genomic regions associated with OC susceptibility, using statistical methods to test associations, validating the identified QTL regions, and analyzing these regions to identify candidate genes responsible for OC susceptibility. This can contribute to better breeding and management strategies to reduce OC prevalence in racehorses.

Step by step solution

01

Reasons for the rising incidence of Osteochondrosis

There could be various reasons for OC incidence rising in racehorses, including genetic factors, breeding practices, and environmental factors. Some possible reasons might include: 1. Selective breeding: Breeding practices that focus on certain traits, like speed and endurance, may inadvertently select for genes associated with OC. This could lead to an increase in the incidence of OC in the racehorse population over time. 2. Increased stress on joints: Racehorses are often subjected to intense physical training and competition, which puts pressure on their joints. This additional stress could contribute to the development of OC. 3. Nutritional factors: Changes in feeding practices or diets could impact the development of OC in horses, especially considering the crucial role of nutrition in the growth of bone and cartilage.
02

Quantitative Trait Locus (QTL) analysis for detecting OC susceptibility

QTL analysis is a statistical method that can be used to identify the genomic regions associated with a quantitative trait, like the susceptibility to OC in horses. Here is a step-by-step description of how to detect OC susceptibility with the help of QTL analysis: 1. Phenotypic data collection: Collect phenotypic data on a sample of horses, including information on the presence or absence of OC, as well as other quantitative traits that may be related to OC susceptibility. 2. Genotyping: Obtain genotypic data for the same sample of horses using high-density SNP (Single Nucleotide Polymorphism) genotyping arrays. This will provide information on each horse's genetics, which can be used in conjunction with the phenotypic data to detect potential associations. 3. Mapping: Perform linkage analysis to identify regions of the genome that may be associated with OC susceptibility. This involves examining the co-segregation of SNP markers with the OC trait to identify regions that are likely to harbor genes responsible for susceptibility. 4. Statistical analysis: Use statistical methods, such as linear regression or mixed models, to test the association between individual SNP markers and OC susceptibility, while accounting for the relatedness among individuals and population structure. 5. Validation: Validate the identified QTL regions by performing functional studies or by examining their role in independent horse populations. This can help to confirm the associations and narrow down the candidate genes for further investigation. 6. Identification of candidate genes: Analyze the QTL regions to identify candidate genes that might be responsible for OC susceptibility. This can be done through bioinformatics analyses, gene expression studies, or functional studies in model organisms. Ultimately, QTL analysis can contribute to a better understanding of the genetic factors underlying OC susceptibility in horses, and ultimately help in the development of breeding and management strategies to reduce the prevalence of this debilitating condition in racehorses.

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Most popular questions from this chapter

Define the following: (a) polygenic, (b) additive alleles, (c) correlation, (d) monozygotic and dizygotic twins, (e) heritability, (f) \(\mathrm{QTL},\) and \((\mathrm{g})\) continuous variation.

Height in humans depends on the additive action of genes. Assume that this trait is controlled by the four loci \(\mathrm{R}, \mathrm{S}, \mathrm{T}\) and \(\mathrm{U}\) and that environmental effects are negligible. Instead of additive versus nonadditive alleles, assume that additive and partially additive alleles exist. Additive alleles contribute two units, and partially additive alleles contribute one unit to height. (a) Can two individuals of moderate height produce offspring that are much taller or shorter than either parent? If so, how? (b) If an individual with the minimum height specified by these genes marries an individual of intermediate or moderate height, will any of their children be taller than the tall parent? Why or why not?

An inbred strain of plants has a mean height of \(24 \mathrm{cm} .\) A second strain of the same species from a different geographical region also has a mean height of \(24 \mathrm{cm} .\) When plants from the two strains are crossed together, the \(\mathrm{F}_{1}\) plants are the same height as the parent plants. However, the \(\mathrm{F}_{2}\) generation shows a wide range of heights; the majority are like the \(P_{1}\) and \(F_{1}\) plants, but approximately 4 of 1000 are only \(12 \mathrm{cm}\) high and about 4 of 1000 are \(36 \mathrm{cm}\) high. (a) What mode of inheritance is occurring here? (b) How many gene pairs are involved? (c) How much does each gene contribute to plant height? (d) Indicate one possible set of genotypes for the original \(P_{1}\) parents and the \(\mathrm{F}_{1}\) plants that could account for these results. (e) Indicate three possible genotypes that could account for \(\mathrm{F}_{2}\) plants that are \(18 \mathrm{cm}\) high and three that account for \(\mathrm{F}_{2}\) plants that are \(33 \mathrm{cm}\) high.

A dark-red strain and a white strain of wheat are crossed and produce an intermediate, medium-red \(\mathrm{F}_{1}\). When the \(\mathrm{F}_{1}\) plants are interbred, an \(\mathrm{F}_{2}\) generation is produced in a ratio of 1 darkred: 4 medium-dark-red: 6 medium-red: 4 light-red: 1 white. Further crosses reveal that the dark-red and white \(\mathrm{F}_{2}\) plants are true breeding. (a) Based on the ratios in the \(\mathrm{F}_{2}\) population, how many genes are involved in the production of color? (b) How many additive alleles are needed to produce each possible phenotype? (c) Assign symbols to these alleles and list possible genotypes that give rise to the medium-red and light-red phenotypes. (d) Predict the outcome of the \(F_{1}\) and \(F_{2}\) generations in a cross between a true-breeding medium-red plant and a white plant.

In a series of crosses between two true-breeding strains of peaches, the \(F_{1}\) generation was uniform, producing 30 -g peaches. The \(\mathrm{F}_{2}\) fruit mass ranges from 38 to \(22 \mathrm{g}\) at intervals of \(2 \mathrm{g}\) (a) Using these data, determine the number of polygenic loci involved in the inheritance of peach mass. (b) Using gene symbols of your choice, give the genotypes of the parents and the \(\mathrm{F}_{1}\).

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