Serum esterase genetics in rabbits. II. Genetic analysis of the prealbumin esterase system,including atropinesterase and cocainesterase polymorphism

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^F 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 ^F 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 α-naphthylacetate only in the presence of the F zones. Est-1 and Est-2 loci are closely linked (<0.5% 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).     

Serum esterase genetics in rabbits. I. Phenotypic variation of the prealbumin esterases and classification of atropinesterase and cocainesterase

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 exclusively responsible for the hydrolysis of cocaine and atropine, respectively. There is an interdependence of the S, F, and D zones: the activity of zone D depends on the presence of the three F zones, whereas these F zones are found only in combination with the three S zones. α-Naphthylacetate as a substrate reveals six different phenotypes; two of these phenotypes are shown to be composed of two subtypes when a supplementary staining procedure is executed. Atropinesterase and cocainesterase are classified as carboxylesterases (E.C. 3.1.1.1.) with a rather wide specificity for both aliphatic and aromatic esters. The α-naphthol esters are split better than the corresponding β-naphthol esters. Naphthol esters with an acyl side-chain of three carbon atoms are hydrolyzed optimally by the enzymes.     

Genetics of two tissue esterase polymorphisms (Est-4 and Est-5) in the rabbit

Two polymorphic esterase systems were found after electrophoresis of rabbit tissue homogenates. Each of these systems is controlled by an autosomal locus with two alleles. Est-4 determines the absence (Est-4^a) or presence (Est-4^b) of two bands of esterase activity with intermediate anodal mobility and broad substrate specificity. This polymorphism was found to be present in liver, small intestine, and spleen but not in kidney, heart, and testis. Est-5 is coding for cathodally migrating esterases which differ in mobility (Est-5^a and Est-5^b). This polymorphism was found only in kidney and testis homogenates. Est-5 esterases are more active against -naphthyl acetate than against -naphthyl acetate and have no activity against -naphthyl butyrate. Linkage analysis indicated that Est-4 is localized on rabbit LG VI as part of a cluster of esterase loci, whereas Est-5 segregates independently. Rabbits from two inbred and nine partly inbred strains were tested for these polymorphisms.This investigation was supported in part by Public Health Service Research Grant RR-00251 from the Division of Research Resources and by funds from the University of Utrecht. The Jackson Laboratory is fully accredited by the American Association for Accreditation of Laboratory Animal Care.     

A third allele at the phosphoglucose isomerase locus of the Japanese quail

Phosphoglucose isomerase electrophoretic patterns of the Japanese quail were found to be controlled by three alleles at an autosomal locus. In the laboratory quail population, the frequency of the alleles PGI^F, PGI^S1 and PGI^S2 was 0.175, 0.465 and 0.360, respectively.     

Evidence for a new allele at the esterase D (E.C.3.1.1.1) locus

A new rare allele for esterase D (ESD) is described in a family from Düsseldorf. The variant was tentatively named ESD Düs 2.     

Serum esterase genetics: Identification and hormone induction of the Es-1b esterase in inbred rats

A previously unrecognized esterase from the sera of the appropriate strains of the rat Rattus norvegicus was revealed by a discontinuous polyacrylamide gel electrophoretic technique. This esterase migrated in the albumin region, whereas a previously known major albumin esterase controlled by the Es-2 locus migrated in the postalbumin region when the method was used. The new albumin esterase component which separated from the Es-2 esterase was identified as the product of the Es-1b gene. The new albumin esterase was not detectable in the sera of sexually mature males of the appropriate genotype, because the activity level of this esterase was influenced by sex hormones, especially androgen.     

Serum esterase genetics in rats: Two new alleles at Es-2, a new esterase regulated by hormonal factors,and linkage of these loci to the Ag-C blood group locus

Two new alleles at the Es-2 locus are described which determine electrophoretic variants of serum esterases of rats. A new esterase protein is described which is detectable in sera of sexually mature females of the appropriate genotype. Evidence is presented for genetic linkage between the Ag-C blood group locus and Es-1, Es-2, and the locus controlling the sex-influenced protein. Since the Ea-1 blood group locus of mice is linked to four esterase loci, it is suggested that Ag-C is the rat homologue of the mouse Ea-1 locus.This work was supported by U.S.P.H.S. Grants AI-09275, CA-15146, and CA-10097.     

The genetics of a new mutable allele at the white locus in Drosophila melanogaster

Summary The genetics of a third case of high mutation frequency at the white locus in Drosophila melanogaster has been analyzed. The new mutable allele, w ^+u, mutates from a wild-type to a white-eyed phenotype in both males and females. The mutational event is 1) premeiotic, 2) not associated with crossingover, 3) sensitive to genetic modification, and 4) restricted to germinal tissue. The only mutants produced by w ^+u are deletions of the white locus. These deficiencies include subsites 4 and 5 of the white locus, but are cytologically unobservable. The mutable allele itself maps to subsite 4.The mutational properties of w ^+u are unlike those of the other highly mutable white alleles which have been interpreted in terms of phage-like controlling elements. Rather, the properties of w ^+u favor a model based on the premature termination of chromosome replication near the terminus of a replicon which leads to a chromosome deficient for the material between the point of premature termination and the end of the replicon.Supported by NIH predoctoral traineeship GM-150 and by NIH research grant GM-07428 to Dr. W. K. Baker.From a dissertation submitted to the Division of Biological Sciences of The University of Chicago in partial fulfillment of the requirements for the degree of Doctor of Philosophy.     

A third allele in the horse albumin system

Starch gel electrophoresis according to Gahne (1966) reveals three new phenotypes designated FI, I and IS in horse serum albumin. Family material comprising 97 sire families with a total number of 2742 foals and their dams and population material comprising 2867 adult horses representative of the Swedish Trotter breed were examined. The results were consistent with a genetic theory of three codominant, autosomal alleles F, I and S controlling the six albumin phenotypes observed. The gene frequencies were estimated to be 0.489, 0.049 and 0.462, respectively, for the F, I and S genes in the Swedish Trotter breed. The risk of making false exclusions in paternity controls in the albumin system, if the I allele is not considered, is discussed.     

Internode length in Pisum. A new allele at the Lh locus

A new allele at the Lh locus has been identified in Pisum sativum L. and named lhⁱ . This allele results in reduced GA levels in young shoots, and a dwarf phenotype. Gas chromatography-selected ion monitoring (GC-SIM) with dideuterated internal standards has been used to demonstrate a quantitative relationship between the level of endogenous GA₁ and internode length using the three alleles ( Lh, lh and lhⁱ ) at the Lh locus. These results are consistent with previous findings in peas (for alleles at the Le locus) and other species possessing a predominant early 13-hydroxylation pathway for GA biosynthesis and support the role of GA₁ as the major native GA in peas with biological activity in its own right. However, in contrast to alleles at the Le locus, GA₂₀ levels are also reduced in lh and lhⁱ plants. The lhⁱ allele also has possible pleiotropic effects on seed abortion, leading to a reduction in seed yield compared to plants homozygous for the previously characterised Lh or lh alleles.     

A new allele at the Pgd locus in pigs

A new electrophoretic variant of porcine 6-phosphogluconate dehydrogenase (PGD) is described. The new variant, PGD C, has been shown to be controlled by a third allele, PgdC, at the Pgd locus.     

Note on a third allele in the erythrocytic NP system of cattle.

A bull ('Mercure') with an erythrocytic NP (nucleoside phosphorylase), phenotype showing a slightly higher anodal mobility has been found. His progeny data generally support the hypothesis of a third F allele in addition to the more common S and the L alleles, resulting in an ABO-like system.     

The genetics of esterase 12 and esterase 13 polymorphisms in the Norway rat

2 new esterase polymorphisms (Es-12 and Es-13) were discovered in haemolysates of wild rats (Rattus norvegicus) by gel electrophoresis. Both loci are probably monomeric. Linkage analysis indicates that neither locus is associated with the esterase cluster in linkage group V.     

Est-2 and Est-3 polymorphisms in Culex pipiens L. from southern France in relation to organophosphate resistance

Est-2 and Est-3 linkage disequilibrium was investigated in 43 natural populations. An association between Est-2 ^0.64 and Est-3 ^A alleles (or its reverse, Est-3 ^Null and alleles other than Est-2 ^0.64) was not observed in 19 (1.2%) of the 1599 mosquitoes analyzed, whereas it should have been found in nearly 400 (25%) individuals if the two loci were in equilibrium. This observation is discussed in relation to organophosphate resistance and genetic distance of the two genes.