Pet-Specific Care for the Veterinary Team. Группа авторов

instead of a three‐number sequence, you have an amino acid sequence of nucleotide triplets (e.g., CAT–TAG–GAC–ATT) that can code for an almost endless array of proteins.

      3.1.4 Mutations

      DNA stores biological information and that information is conserved and replicated as the strands peel apart and are duplicated. Just like a photocopier, cells copy the DNA throughout an animal's life as cells are replenished and, for the most part, there are very few errors in the duplication process.

Genetic diseases usually cause problems because a mutation creates a poorly functioning facsimile of the normal gene product (Box 3.1.1). Such a mutation often happens because of innocent‐appearing mishaps that result in an altered product.

Box 3.1.1 Story of a mutation

      We know that the genetic code is actually written with triplet codons, such that three nucleotide bases together code for a single amino acid. Thus, using the four bases, adenine (A), thymine (T), guanine (G), and cytosine (C), we can construct a chain of bases that code for amino acids that will form an enzyme, a protein, or a polypeptide. DNA is read three bases at a time, and these three bases correspond to specific amino acids. Accordingly, TATAGACAACAT would be read as tyrosine (TAT)–arginine (AGA)–glutamine (CAA)–histidine (CAT).

      Redundancy is built into the system. For example, both TAC and TAT code for tyrosine, so if the T in position 3 happens to be replaced by the base C, the final product is not affected (a silent mutation). Now, given the previous sequence, imagine that a point mutation occurs that deletes the third base in the sequence (T). With the bases after that point shifting one to the left, the first codon becomes TAA, which is a stop codon and arrests the process. If the deletion were to occur to the fourth base (A), the resulting peptide would be changed to tyrosine (TAT)–aspartic acid (GAC)–asparagine (AAC), which is completely different from the peptide normally produced.

      Even though DNA replication is remarkably efficient, mistakes occasionally do happen. A base substitution that results in a stop codon, prematurely halting the process, is called a nonsense mutation; the resulting polypeptide will be shorter than usual and probably not functional. Progressive retinal atrophy (PRA) in the Irish setter, for example, is the result of a nonsense mutation in the cGMP‐phosphodiesterase‐beta gene. A missense mutation occurs when one base is substituted for another, which potentially results in a different amino acid occurring in the chain.

      In some cases, the resultant polypeptide may not be functional. In other cases, however, because of redundancy built into the system, a base substitution will not change the amino acid product (e.g., CAT and CAC both code for histidine). This substitution is referred to as a silent mutation. Hemophilia B is characterized by a substitution of A for G at nucleotide 1477 in the gene for canine factor IX, resulting in the substitution of glutamic acid for glycine at position 379 in the factor IX molecule, which decreases the efficiency of blood clotting.

      In contrast to missense mutations, in which only one amino acid in a sequence is affected, if a base is inserted or deleted in the DNA strand, it has the potential to alter the reading of the entire coded sequence downstream because the triplet codons are now out of their original sequence. This mutation is known as a frameshift mutation, an example of which is X‐linked nephritis. In simple terms, take the phrase “how are you” and insert the letter b after the letter h in how to see how a simple insertion of one base can change expression. The shift results in “hbo war eyo u” which doesn't communicate the same message as “how are you.” You can imagine what would happen to a genetic sequence in the same circumstances.

      Considering that a point mutation happens by chance, that it can affect any bases in a DNA sequence for a peptide, and it then passes to future generations, it should not be surprising that similar disorders in different breeds can result from very different gene mutations. That is why the DNA test for PRA in Irish setters will not work in miniature poodles. Although the final clinical result of PRA is similar, the underlying genetic disorder could not be more different. When the incidence of mutations is combined with the fact that about 70% of all mutations are recessive, it is not difficult to see how they can be propagated.

      3.1.5 Propagation of Traits

      If you have a breeding animal that has superior attributes (phenes) but inadvertently carries a recessive trait that is not clinically evident even to the trained eye (genes are read in pairs, and if one of those pairs reflects a recessive trait, then the trait will not be displayed), then the pet may be bred intensively. If that recessive trait is not present in the other breeding stock, all the offspring (F1 generation) will appear clinically (phenotypically) normal, but some of the offspring will still carry that recessive trait. If that generation is bred to unrelated stock, all the next generation (F2) will also be phenotypically normal, with even a smaller percentage being carriers. If bred to related stock that also carry the mutation, however, the recessive trait will begin to be concentrated and manifested.

      3.1.6 Microsatellites

      In a simple world, as described earlier, one might consider the genome as a passenger train, with the genes as railway cars coupled to one another. In reality, it is not that orderly. This unsophisticated look is what provides an opportunity to learn a lot from the genome. If the genome were arranged like a train, researchers would have to isolate each gene (passenger car) to learn anything. Fortunately, however, nature has provided spacers, known as microsatellites, that can act as markers for traits. They might be considered as dining cars spaced between groups of passenger cars.

      As more and more useful microsatellites are identified, a higher resolution map of the genome will continue to be developed of which markers are inherited along with specific genes. Then, by measuring these markers, we can tell with some accuracy an individual's genetic make‐up for that specific trait without having to necessarily identify the actual gene. This can be very helpful when trying to predict some disorders which are unlikely to be completely controlled by individual genes alone (e.g., hip dysplasia, atopic dermatitis, etc.).

      To use the train example once more, when train cars are unhitched and transferred to other trains, which passenger cars always seem to go along with the same dining car? If you identify a specific dining car, you know which passenger cars are also likely to be found there, too. Obviously, the closer the gene (passenger car) is to the marker (dining car), the greater is the probability that the two will be transferred together. A gene that is farther away from the marker may not be transferred 100% of the time, which would affect a test's specificity and predictive ability. Thus, some microsatellite markers may be associated with increased risk of a condition, and others with decreased risk, and when considered in aggregate, they could provide an impression of the risk for such traits in individual animals.

      Microsatellites have more to offer than just their role as signposts. They have considerable variability (which molecular geneticists call polymorphism), making them unique identifiers of individuals and their offspring. Variations in a DNA sequence are called SNPs, some of which have no impact on health while others may predispose an individual to disease or signal responsiveness to medical therapies. Microsatellites are one way to identify an individual, as well as its progeny, and have become a voluntary part of the DNA identification for the different purebred registries. If a sire has six repetitive sequences relative to a specific marker and the dam has eight, the offspring will have one copy from each parent. By comparing findings at multiple markers, the accuracy of predicting parentage becomes a virtual certainty.

      Short interspersed elements are often inserted within or near genes and may regulate their expression. The pet population has thousands of short interspersed element differences, which are associated with breed differences related to behavioral and physical characteristics and also act as signposts for specific genes linked to disease susceptibility or traits.