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Genetic aspects of umbilical hernia incidence in cats and dogs
The Veterinary Record
|January 1, 1977
Abstract:
The incidence of umbilical hernia in a family of Cornish rex cats approximated monogenic proportions. The genetic and developmental basis for umbilical hernia may be similar in cats and dogs. The defect is probably a polygenic threshold character, possibly involving a major gene whose expression is mediated by the genetic (breed) background.
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Pedigree Analysis
Overview
Genomic Imprinting and Inheritance
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
Nondisjunction
Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This produces daughter cells with abnormal chromosome numbers. Nondisjunction is common during anaphase I or anaphase II of meiosis. Mutations in synaptonemal complex proteins that attach homologous chromosomes increase the chances of nondisjunction in anaphase I of meiosis I. In contrast, mutations in topoisomerases and condensins that hold sister...

