Allelic Variability in Species and Stocks of Lake Superior Ciscoes (Coregoninae)

1981 ◽  
Vol 38 (12) ◽  
pp. 1808-1813 ◽  
Author(s):  
Thomas N. Todd
Keyword(s):  
Lake Superior ◽  
Random Mating ◽  
Starch Gel Electrophoresis ◽  
Morphological Criteria ◽  
Mating Population ◽  
Allelic Variability ◽  
Starch Gel ◽  
Coregonus Artedii ◽  
Glycerol 3 Phosphate Dehydrogenase ◽  
Do So

Starch gel electrophoresis was used as a means of recognizing species and stocks in Lake Superior Coregonus. Allelic variability at isocitrate dehydrogenase and glycerol-3-phosphate dehydrogenase loci was recorded for samples of lake herring (Coregonus artedii), bloater (C. hoyi), kiyi (C. kiyi), and shortjaw cisco (C. zenithicus) from five Lake Superior localities. The observed frequencies of genotypes within each subsample did not differ significantly from those expected on the basis of random mating, and suggested that each subsample represented either a random sample from a larger randomly mating population or an independent and isolated subpopulation within which mating was random. Significant contingency χ2 values for comparisons between both localities and species suggested that more than one randomly mating population occurred among the Lake Superior ciscoes, but did not reveal how many such populations there were. In contrast to the genetic results of this study, morphology seems to be a better descriptor of cisco stocks, and identification of cisco stocks and species will still have to be based on morphological criteria until more data are forthcoming. Where several species are sympatric, management should strive to preserve the least abundant. Failure to do so could result in the extinction or depletion of the rarer forms.Key words: Coregonus, electrophoresis, genetic heterogeneity, speciation, Great Lakes

Survey of the Genetic Variation Among Eastern Lake Superior Lake Trout (Salvelinus namaycush)

1981 ◽  
Vol 38 (12) ◽  
pp. 1738-1746 ◽  
Author(s):  
Terrence R. Dehring ◽  
Anne F. Brown ◽  
Charles H. Daugherty ◽  
Stevan R. Phelps
Keyword(s):  
Genetic Variation ◽  
Gel Electrophoresis ◽  
Lake Trout ◽  
Lake Superior ◽  
Salvelinus Namaycush ◽  
Starch Gel Electrophoresis ◽  
Average Heterozygosity ◽  
Management Implications ◽  
Salmonid Species ◽  
Starch Gel

Patterns of genetic variation among lake trout (Salvelinus namaycush) of eastern Lake Superior were examined using starch gel electrophoresis. We used 484 individuals sampled from three areas, representing three morphological types (leans, humpers, and siscowets). Of 50 loci examined, 44 were monomorphic in all groups sampled. Genetic variation occurs at six loci AAT-1,2, MDH-3,4, ME-1, and SOD-1. The average heterozygosity found (H = 0.015) is low relative to other salmonid species. A significant amount of heterogeneity exists among the 10 lake trout samples. These differences are due to variation within as well as between morphological types. The significance and management implications of these data are discussed.Key words: genetic variation, lake trout, Salvelinus namaycush, Lake Superior

Genetic structure and mating system of white spruce (Piceaglauca) in a seed production area

1984 ◽  
Vol 14 (5) ◽  
pp. 639-643 ◽  
Author(s):  
John N. King ◽  
Bruce P. Dancik ◽  
Narinder K. Dhir
Keyword(s):  
Genetic Structure ◽  
Mating System ◽  
Seed Production ◽  
Gel Electrophoresis ◽  
Random Mating ◽  
White Spruce ◽  
Starch Gel Electrophoresis ◽  
Starch Gel ◽  
Production Area ◽  
Mating Model

Embryos and megagametophytes of open-pollinated seed of 37 white spruce (Piceaglauca (Moench) Voss) trees from a seed production area were analyzed by starch gel electrophoresis to determine the genetic structure and mating system over 2 seed crop years. Analysis of four polymorphic enzyme loci (Gdh, Idh, Pgm, and Pgi-2) for spatial and temporal genetic structure and mating system indicated substantial deviations from the random mating model that is assumed when open-pollinated families are designated as half-sibs.

Genetics of Glycerol-3-phosphate Dehydrogenase Isozymes in White Muscle of Lake Whitefish (Coregonus clupeaformis)

1973 ◽  
Vol 30 (2) ◽  
pp. 187-193 ◽  
Author(s):  
J. W. Clayton ◽  
W. G. Franzin ◽  
D. N. Tretiak
Keyword(s):  
White Muscle ◽  
Natural Populations ◽  
Heat Inactivation ◽  
Starch Gel Electrophoresis ◽  
Coregonus Clupeaformis ◽  
Lake Whitefish ◽  
Red Muscle ◽  
Catalytically Active ◽  
Coregonus Artedii ◽  
Glycerol 3 Phosphate Dehydrogenase

Multiple isozymes of glycerol-3-phosphate dehydrogenase (L-gIycerol-3-phosphate: NAD oxidoreductase, E. C. 1.1.1.8) have been resolved by starch gel electrophoresis of extracts of muscle tissue from lake whitefish (Coregonus clupeaformis). The isozyme electropherograms show that three kinds of subunit, A, B, and C, are synthesized in red muscle and two of these, A and B, are also found in white muscle. In red muscle the subunits evidently combine to form catalytically active dimers of the following types: AA, AB, BB, BC, and CC. In white muscle only the AA, AB, and BB dimers were observed.A genetic and molecular structure model is proposed for the glycerol-3-phosphate dehydrogenase (G-3-PDH) isozymes in white muscle of lake whitefish. On the basis of two alleles for A subunits and three alleles for B subunits, the model predicts a total of 18 distinct, electrophoretic G-3-PDH phenotypes for all possible AA, AB, and BB dimeric isozymes. The model has been confirmed by the results of a breeding experiment that tested the heritability of each of the five known alleles. A difference in the rate of heat inactivation of AA and BB isozymes was also interpreted as additional evidence for the unique genetic and molecular nature of the two kinds of subunits.Surveys of natural populations of lake whitefish revealed some marked variations in the frequencies of G-3-PDH alleles in fish from different geographical areas.The cisco (Coregonus artedii) also appears to have three "b" alleles for G-3-PDH.

A new species ofChthamalus(Crustacea: Cirripedia) characterized by enzyme electrophoresis and shell morphology: with a revision of other species ofChthamalusfrom the western shores of the atlantic ocean

1980 ◽  
Vol 60 (3) ◽  
pp. 787-831 ◽  
Author(s):  
P. R. Dando ◽  
A. J. Southward
Keyword(s):  
Gel Electrophoresis ◽  
Distinct Species ◽  
Morphological Characters ◽  
Shell Morphology ◽  
Enzyme Electrophoresis ◽  
Starch Gel Electrophoresis ◽  
Morphological Criteria ◽  
Starch Gel ◽  
Simple Measurement ◽  
A New Species

Chthamalus proteussp. nov. is described as a distinct species based on its clear separation by starch-gel electrophoresis of enzymes. A redescription is given ofC. fragilis, a related species, which differs absolutely fromC. proteusin 3 out of 16 enzymes. Given the distinction ofC. proteusfromC. fragilisby enzyme methods, it has been possible to devise morphological criteria, involving simple measurement of the opercular valves and first maxilla, which can separate the two species in 99% of individuals. Although the morphological characters overlap slightly, the enzyme results show no evidence of hybridization. A species previously confused withC. proteus, C. bisinuatusfrom Brazil, differs considerably in morphology and is briefly redescribed.

Bovine Platelet Proteins II. Purification of Platelet Fibrinogen

1969 ◽  
Vol 21 (03) ◽  
pp. 419-427 ◽  
Author(s):  
N. O Solum ◽  
S Łopaciuk
Keyword(s):  
Analytical Ultracentrifugation ◽  
Insoluble Fraction ◽  
Disc Electrophoresis ◽  
Plasma Fibrinogen ◽  
Starch Gel Electrophoresis ◽  
Freezing And Thawing ◽  
Insoluble Material ◽  
High Resolution Power ◽  
Starch Gel ◽  
Platelet Proteins

Summary1. Platelet fibrinogen has been purified from washed bovine platelets. The procedure was based on the methods for purification of plasma fibrinogen by fractionated precipitations and extractions with ethanol and glycine below 0°, and precipitation of proteins by dimethylformamide at 0°.2. The platelet extract obtained by freezing and thawing of the cells, freed from insoluble material by centrifugation at 23,000 x g for 30 min, contained 0.22 ±0.003mg fibrinogen per 109 platelets. Total protein of this fraction was 0.77 ±0.08 mg per 109 platelets whereas that of the insoluble fraction was 0.79 ±0.09 mg per 109 platelets.3. The most purified platelet fibrinogen fraction contained 91-98% of the protein in a thrombin-clottable state. The yield was approx. 20%. It showed homogeneity in analytical ultracentrifugation, in immunoelectrophoresis using an antiserum produced by immunization of rabbits against platelet extract, and in starch gel electrophoresis using a discontinuous system of Tris HCl and borate buffers offering a high resolution power towards the platelet proteins. Polyacrylamide disc electrophoresis revealed two to three faint lines behind the main fibrinogen line. At least one such line was also observed with purified plasma fibrinogen.

Fractionation of Plasminogen by Starch Gel Electrophoresis

1964 ◽  
Vol 12 (01) ◽  
pp. 126-136 ◽  
Author(s):  
Karl H. Slotta ◽  
J. D Gonzalez
Keyword(s):  
Gel Electrophoresis ◽  
Room Temperature ◽  
Broad Band ◽  
Caproic Acid ◽  
Starch Gel Electrophoresis ◽  
Full Activity ◽  
Veronal Buffer ◽  
Starch Gel ◽  
Alkaline Range

SummaryWhen urea or ε-amino caproic acid were used as solublizing agents for plasminogen in electrophoretic experiments, only one broad band of the proenzyme was obtained on acetate cellulose, in starch block, and in acrylamide gel. In starch gel electrophoresis, however, both forms of plasminogen – the native or euglobulin and Kline’s or Pseudoglobulin plasminogen – separated into six bands. These migrated toward the cathode at room temperature in borate or veronal buffer in the alkaline range and showed full activity in fibrinagar-streptokinase plates.

scholarly journals PROTEIN POLYMORPHISMS, SEGREGATION IN GENETIC CROSSES AND GENETIC DISTANCES AMONG FISHES OF THE GENUS XIPHOPHORUS (POECILIIDAE)

Genetics ◽  
1982 ◽  
Vol 102 (3) ◽  
pp. 539-556
Author(s):  
Don C Morizot ◽  
Michael J Siciliano
Keyword(s):  
Goodness Of Fit ◽  
Inbred Strains ◽  
Interspecific Backcross ◽  
Genetic Distances ◽  
Rapid Expansion ◽  
Starch Gel Electrophoresis ◽  
Lower Vertebrate ◽  
Protein Coding ◽  
Group I ◽  
Starch Gel

ABSTRACT The products of 49 protein-coding loci were examined by starch gel electrophoresis for populational variation in six species of Xiphophorus fishes and/or segregation in intra- and interspecific backcross and intercross hybrids. Electrophoretic variation was observed for 29 of the 35 locus products in a survey of 42 population samples. The highest frequency of polymorphic loci observed in noninbred populations was 0.143. After ten or more generations of inbreeding, all loci studied were monomorphic. Inbred strains generally exhibited the commonest electrophoretic alleles of the population from which they were derived. An assessment of genetic distances among Xiphophorus populations reflected classical systematic relationships and suggested incipient subspeciation between X. maculatus from different drainages as well as several species groups. Thirty-three loci were analyzed with respect to segregation in hybrids. The goodness of fit of segregations to Mendelian expectations at all loci analyzed (except loci in linkage group I) is interpreted as evidence for high genetic compatibility of the genomes of Xiphophorus species. It is anticipated that these data will result in a rapid expansion of the assignment of protein-coding loci to linkage groups in these lower vertebrate species.

scholarly journals THE INHERITANCE OF ENZYME VARIANTS FOR TYROSINE AMINOTRANSFERASE, NADP-DEPENDENT MALATE DEHYDROGENASE, NADP-DEPENDENT ISOCITRATE DEHYDROGENASE, AND TETRAZOLIUM OXIDASE IN TETRAHYMENA PYRIFORMIS, SYNGEN 1

Genetics ◽  
1973 ◽  
Vol 74 (4) ◽  
pp. 595-603
Author(s):  
D Borden ◽  
E T Miller ◽  
D L Nanney ◽  
G S Whitt
Keyword(s):  
Detailed Analysis ◽  
Malate Dehydrogenase ◽  
Isocitrate Dehydrogenase ◽  
Gel Electrophoresis ◽  
Tetrahymena Pyriformis ◽  
Tyrosine Aminotransferase ◽  
Breeding Program ◽  
Starch Gel Electrophoresis ◽  
Enzyme Locus ◽  
Starch Gel

ABSTRACT The isozymic patterns of tyrosine aminotransferase, NADP malate dehydrogenase, NADP isocitrate dehydrogenase, and tetrazolium oxidase were examined by starch-gel electrophoresis in Tetrahymena pyriformis, syngen 1. The genetics of the alleles controlling these enzymes was studied through a breeding program. Each enzyme locus was shown to assort vegetatively, as do other loci in this organism. A detailed analysis of the assortment process for the tyrosine aminotransferase locus indicated that the rate of stabilization of heterozygotes into pure types was essentially identical to previously-reported rates for other loci.

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