GENETICS OF GLOSSINA MORSITANS MORSITANS (DIPTERA: GLOSSINIDAE): I. ELECTROPHORETIC BANDING PATTERNS OF XANTHINE OXIDASE AND ALDEHYDE OXIDASE

1978 ◽  
Vol 110 (12) ◽  
pp. 1233-1239 ◽  
Author(s):  
B.M. Rolseth ◽  
R.H. Gooding
Keyword(s):  
Xanthine Oxidase ◽  
Aldehyde Oxidase ◽  
Glossina Morsitans Morsitans ◽  
Single Locus ◽  
Glossina Morsitans ◽  
Gene Frequencies ◽  
University Of Alberta ◽  
Laboratory Populations ◽  
University Of Bristol ◽  
The University

AbstractPolyacrylamide gel (6%) electrophoresis (at pH 8.2) of the thoraces of adult Glossina morsitans morsitans Westwood revealed three xanthine oxidase (XO) phenotypes and six aldehyde oxidase (AO) phenotypes. Each enzyme was postulated to be under the control of a single locus, XO with two alleles and AO with three alleles. Gene frequencies were in Hardy-Weinberg equilibrium for both loci in two laboratory populations. Breeding experiments provided direct evidence for single locus control of each enzyme. No significant differences in phenotype frequencies were observed between the colony maintained at the University of Alberta, Canada and the parent colony at the University of Bristol, England. A colony of highly inbred flies from the University of Bristol had only one phenotype of AO and of XO.

GENETICS OF GLOSSINA MORSITANS MORSITANS (DIPTERA: GLOSSINIDAE): II. ELECTROPHORETIC BANDING PATTERNS OF MIDGUT ALKALINE PHOSPHATASE

1978 ◽  
Vol 110 (12) ◽  
pp. 1241-1246 ◽  
Author(s):  
R. H. Gooding ◽  
B. M. Rolseth
Keyword(s):  
Alkaline Phosphatase ◽  
Glossina Morsitans Morsitans ◽  
Single Locus ◽  
Glossina Morsitans ◽  
Gene Frequencies ◽  
Ph Optimum ◽  
Banding Patterns ◽  
Laboratory Populations ◽  
Hardy Weinberg Equilibrium ◽  
Alkaline Phophatase

AbstractThe digestive section of the midgut of Glossina morsitans morsitans Westwood contains a phosphatase with a pH optimum of approximately 9.2 and with low substrate specificity; the enzyme was classified as an alkaline phosphatase (E.C. 3.1.3.1).Polyacrylamide gel (6%) electrophoresis (at pH 8.9) of the digestive portion of the midguts of adult G. morsitans morsitans revealed three alkaline phophatase phenotypes. Midgut phosphatase was postulated to be under control of a single locus (designated alkph) with two alleles. Gene frequencies were in Hardy-Weinberg equilibrium in two laboratory populations while a third, highly inbred population had only one phenotype. Phenotype frequencies were not significantly different among females of various ages from the Edmonton colony. Breeding experiments provided direct evidence for single locus control of midgut phosphatase.

Genetics of Glossina morsitans morsitans (Diptera: Glossinidae). XII. Comparison of field-collected and laboratory-reared flies

1986 ◽  
Vol 28 (6) ◽  
pp. 1016-1021 ◽  
Author(s):  
R. H. Gooding ◽  
A. M. Jordan
Keyword(s):  
Polyacrylamide Gel Electrophoresis ◽  
Glossina Morsitans Morsitans ◽  
Tsetse Fly ◽  
Glossina Morsitans ◽  
University Of Alberta ◽  
Rare Alleles ◽  
Locus Number ◽  
Closed Colony ◽  
University Of Bristol ◽  
The University

Adult Glossina morsitans morsitans Westwood emerging from puparia collected at Rekometjie, Zimbabwe, were compared at 13 loci with G. m. morsitans from a closed colony at the Tsetse Research Labortory (TRL), University of Bristol, by polyacrylamide gel electrophoresis. The populations were not significantly different with respect to mean heterozygosity per locus, average effective number of alleles per locus, number of polymorphic loci, or allele frequencies at 12 loci. (The exception was Alkph.) Rare alleles at To, Est-t, and Alkph were found only in Rekometjie flies while rare alleles at G6pd and Est-2 were found only in TRL flies. No significant level of sterility was found in F1 flies produced in reciprocal crosses of Rekometjie flies with G. m. morsitans from the University of Alberta colony.Key words: Glossina, tsetse fly, isozymes, heterozygosity.

GENETICS OF GLOSSINA MORSITANS MORSITANS (DIPTERA: GLOSSINIDAE): IV. ELECTROPHORETIC BANDING PATTERNS OF OCTANOL DEHYDROGENASE AND ARGININE PHOSPHOKINASE

1979 ◽  
Vol 111 (11) ◽  
pp. 1307-1310 ◽  
Author(s):  
R.H. Gooding ◽  
B.M. Rolseth
Keyword(s):  
Gel Electrophoresis ◽  
Polyacrylamide Gel Electrophoresis ◽  
Aldehyde Oxidase ◽  
Glossina Morsitans Morsitans ◽  
Polyacrylamide Gel ◽  
Single Locus ◽  
Single Individual ◽  
Glossina Morsitans ◽  
Banding Patterns ◽  
Octanol Dehydrogenase

AbstractPolyacrylamide gel electrophoresis of the thoraces of adult Glossina morsitans morsitans Westwood revealed five octanol dehydrogenase (ODH, E.C. 1.1.1.73) phenotypes (and a sixth was predicted) in males and females, two arginine phosphokinase (APK, E.C. 2.7.3.3) phenotypes in males and three APK phenotypes in females. Each enzyme was postulated to be under the control of a single locus; Odh with three alleles on an autosome and Apk with two alleles on the X-chromosome. Allele frequencies were in Hardy-Weinberg equilibrium in our colony, and breeding experiments provided direct evidence for single locus control of each enzyme. The polyacrylamide gel electrophoresis technique described permits determination of banding patterns for xanthine oxidase, aldehyde oxidase, ODH, and APK from a single individual.

GENETICS OF GLOSSINA MORSITANS MORSITANS (DIPTERA: GLOSSINIDAE). VI. MULTILOCUS COMPARISON OF THREE LABORATORY POPULATIONS

1982 ◽  
Vol 24 (1) ◽  
pp. 109-115 ◽  
Author(s):  
R. H. Gooding ◽  
B. M. Rolseth
Keyword(s):  
Malate Dehydrogenase ◽  
Polyacrylamide Gel Electrophoresis ◽  
Aldehyde Oxidase ◽  
Glossina Morsitans Morsitans ◽  
Reproductive Capacity ◽  
Glossina Morsitans ◽  
Geographic Origins ◽  
Laboratory Populations ◽  
The Mean ◽  
Glucose 6 Phosphate Dehydrogenase

Three strains (Kariba, Handeni, and ocra) of Glossina morsitans morsitans Westwood were examined by polyacrylamide gel electrophoresis to determine the extent of genetic similarity among the strains. Males were examined for 11 thoracic enzymes, one testicular enzyme, and one midgut enzyme. Tetrazolium oxidase, manganese stimulated malate dehydrogenase, an alpha-glycerophosophate deyhdrogenase, and testicular esterase were monomorphic. Variation was found in xanthine oxidase, aldehyde oxidase, octanol dehydrogenase, an alpha-glycerophosophate dehydrogenase, malate dehydrogenase, midgut alkaline phosphatase, two esterases, arginine phosphokinase, and glucose 6-phosphate dehydrogenase. Loci for the latter two enzymes are on the X-chromosome; all others are on autosomes. Allele frequencies in the three strains indicated that the Kariba and ocra strains are more closely related to each other than either is to the Handeni strain. These genetic similarities are consistant with the geographic origins of the strains. The mean heterozygosity per locus was highest (16.7% and 16.0%) in the two strains (Kariba and ocra) which have the highest reproductive capacity under laboratory conditions, and lowest (7.3%) in the strain (Handeni) which has the lowest reproductive capacity.

Genetics of Glossina morsitans morsitans (Diptera: Glossinidae). VII. Location of G6pd in linkage group I, and Alkph in linkage group II

1983 ◽  
Vol 25 (1) ◽  
pp. 30-32 ◽  
Author(s):  
R. H. Gooding
Keyword(s):  
Alkaline Phosphatase ◽  
Linkage Group ◽  
Xanthine Oxidase ◽  
Aldehyde Oxidase ◽  
Glossina Morsitans Morsitans ◽  
Body Color ◽  
Glossina Morsitans ◽  
Group I ◽  
Group Ii ◽  
Glucose 6 Phosphate Dehydrogenase

In Glossina morsitans morsitans Westwood the locus for glucose-6-phosphate dehydrogenase, G6pd, was found to be in linkage group I, approximately 35 to 42 map units to the left of ocra, the locus for body color. The locus for midgut alkaline phosphatase, Alkph, was found to be in linkage group II, within 0.41 map units of the locus for xanthine oxidase, Xo. The distance from Xo to the locus for aldehyde oxidase, Ao, was confirmed to be about 42 map units. No evidence for genetical recombination was found in male G. m. morsitans.

Genetics of Glossina morsitans morsitans (Diptera: Glossinidae). XIII. Mapping the locus for tetrazolium oxidase in linkage group I and refinement of the linkage group II map

Genome ◽  
1988 ◽  
Vol 30 (6) ◽  
pp. 885-887 ◽  
Author(s):  
R. H. Gooding ◽  
B. M. Rolseth ◽  
S. A. Tarimo
Keyword(s):  
Linkage Group ◽  
Key Words ◽  
Aldehyde Oxidase ◽  
Glossina Morsitans Morsitans ◽  
Linkage Maps ◽  
Glossina Morsitans ◽  
Eye Color ◽  
Group I ◽  
Group Ii

The locus for tetrazolium oxidase, To, is mapped at 4.3 ± 1.3 recombination units from the locus for arginine phosphokinase, Apk, in linkage group I, and the distance between the eye color locus, sal, and Apk is confirmed to be about 39.5 ± 3.2 recombination units. In linkage group II the loci for aldehyde oxidase, Ao, and for two esterases are arranged in the order Ao Est-1 Est-2 with 3.5 ± 1.2 recombination units separating Ao and Est-1 and 8.3 ± 1.8 recombination units separating Est-1 and Est-2.Key words: Glossina morsitans, tetrazolium oxidase, aldehyde oxidase, esterases, linkage maps.

GENETICS OF GLOSSINA MORSITANS MORSITANS (DIPTERA: GLOSSINIDAE). V. DEFINITION AND PRELIMINARY MAPPING OF LINKAGE GROUPS I AND II

1981 ◽  
Vol 23 (3) ◽  
pp. 399-403 ◽  
Author(s):  
R. H. Gooding
Keyword(s):  
Linkage Group ◽  
X Chromosome ◽  
Aldehyde Oxidase ◽  
Glossina Morsitans Morsitans ◽  
Linkage Groups ◽  
Glossina Morsitans ◽  
Eye Color ◽  
Group I ◽  
Octanol Dehydrogenase ◽  
Differential Part

Linkage group I is defined as the loci on the differential part of the X-chromosome of adult Glossina morsitans morsitans Westwood. Three loci are known and their order on the X-chromosome has been demonstrated as ocra (body color), salmon (eye color), and Apk (arginine phosphokinase, E.C. 2.7.3.3) with 38 map units separating the first two loci and 32 to 41 separating the second two. This region of the X-chromosome does not contain the chromosomal inversion known to occur in the Handeni line of G. m. morsitans. Linkage group II is defined as the autosome carrying the locus Xo (xanthine oxidase, E.C. 1.2.3.2), and it is demonstrated to carry also the loci Ao (aldehyde oxidase, E.C. 1.2.3.1) and Odh (octanol dehydrogenase, E.C. 1.1.1.73). Ao and Odh are within 0.36 map units of each other and have not been separated by recombination; this pair of loci occur about 48 map units from Xo. During mapping experiments, no evidence for genetical recombination was found in male G. m. morsitans.

Genetics of Glossina morsitans morsitans (Diptera: Glossinidae). IX. Definition of linkage group III and further mapping of linkage groups I and II

1984 ◽  
Vol 26 (3) ◽  
pp. 253-257 ◽  
Author(s):  
R. H. Gooding
Keyword(s):  
Linkage Group ◽  
Aldehyde Oxidase ◽  
Glossina Morsitans Morsitans ◽  
Linkage Groups ◽  
Glossina Morsitans ◽  
Malic Dehydrogenase ◽  
Group Iii ◽  
Glycerophosphate Dehydrogenase ◽  
Group I ◽  
The Right

In Glossina morsitans morsitans Westwood, linkage group III is defined as the autosome carrying the locus Mdh (malic dehydrogenase), the only locus so far identified in this linkage group. The locus αGpd.2 (α-glycerophosphate dehydrogenase) was located 45 map units (MU) to the left of Xo (xanthine oxidase) and the loci Est.1 and Est.2 (loci for two esterases found in the thorax) were mapped approximately 5–10 MU to the right of Ao (aldehyde oxidase) in linkage group II. The location of G6pd (glucose-6-phosphate dehydrogenase) has been confirmed to be approximately 37 MU to the left of oc (ocra body color) in linkage group I and it was shown that this region of the X chromosome does not involve the large paracentric inversion found in the Handeni line. A genetic map for 12 loci in the three linkage groups found in G. m. morsitans is presented.Key words: Diptera, Glossina, mapping, inversion, isozymes.

Centres for Health Evidence Demonstration Project

2013 ◽  
Author(s):  
Tracy Stewart ◽  
Denise Koufogiannakis ◽  
Robert S.A. Hayward ◽  
Ellen Crumley ◽  
Michael E. Moffatt
Keyword(s):  
Evidence Based Practice ◽  
Demonstration Project ◽  
Evidence Based ◽  
Research Opportunities ◽  
University Of Alberta ◽  
Information Usage ◽  
University Of Manitoba ◽  
The University ◽  
Hospital Wards ◽  
Support Evidence

This paper will report on the establishment of the Centres for Health Evidence (CHE) Demonstration Project in both Edmonton at the University of Alberta and in Winnipeg at the University of Manitoba. The CHE Project brings together a variety of partners to support evidence-based practice using Internet-based desktops on hospital wards. There is a discussion of the CHE's cultural and political experiences. An overview of the research opportunities emanating from the CHE Project is presented as well as some early observations about information usage.

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