Rabbit atropinesterase and cocainesterase were studied by starch gel electrophoresis. The enzymes are localized in a region of the gels anodal to the albumins (prealbumin esterases). In this region, three groups of esterase zones ( S, F, and D) can be distinguished. The S and F zones are almost excl
Serum esterase genetics in rabbits. II. Genetic analysis of the prealbumin esterase system, including atropinesterase and cocainesterase polymorphism
โ Scribed by L. F. M. Zutphen
- Publisher
- Springer
- Year
- 1974
- Tongue
- English
- Weight
- 675 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0006-2928
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โฆ Synopsis
The zymotypic variation of rabbit prealbumin esterases is controlled by three autosomal loci, each with two alleles: Est-1 s and Est-1 s, Est-2 v and Est-2 f', Est-3 D and Est-3 d. Est-1 s gives rise to the three S zones possessing the cocainesterase activity, Est-2 v to the three F zones with atropinesterase activity. Presence of the latter allele is never manifested without the Est-1 s allele. Est-3 D codes for the D zone. This D esterase reacts with the currently used substrate ~-naphthylacetate only in the presence of the F zones. Est-1 and Est-2 loci are closely linked (<0.5%o recombination); Est-3 shows no coupling with Est-1 and Est-2. The Est-1 s and Est-3 D alleles have a complete dominant expression, whereas the Est-2 alleles are codominant. Gene frequencies of the Est-1 and Est-2 loci vary between the examined breeds. A Hardy-Weinberg equilibrium is found in two populations (Cpb:ALU and Cpb: VW). A significant surplus of heterozygotes is demonstrated in a third population (Cpb:CH).
๐ SIMILAR VOLUMES
Discontinuous starch gel electrophoresis revealed a fourth allele of rabbit pre-albumin serum esterase at locus Est-2. This allele is designated Est-2f and appears to be silent. In addition to the prealbumin serum esterases, another serum esterase system was studied in rabbits. This system is locali