Allozymes and genetic variability in Medicago turbinata, M. truncatula, and their hybrids

1983 ◽  
Vol 25 (3) ◽  
pp. 286-291 ◽  
Author(s):  
Carlos F. Quiros ◽  
Lisa Ostafichuk

The genetic variability in the diploid annual species (2n = 2x = 16) Medicago turbinata L. and M. truncatula Gaernt. was studied at three loci for the enzymes peroxidase, Prx1-1, and leucine-aminopeptidase, Lap1-1 and Lap1-2. Eight accessions of each species, including all the taxonomic forms were surveyed by starch gel electrophoresis. No variation was observed among plants within each accession. Among the M. turbinata forms, four alleles were observed at locus Lap1-2. No variation was detected for the other two loci studied. For the M. truncatula forms, four alleles were found for Prx1-1 and three alleles for Lap1-2. No variation was observed for locus Lap1-1. Form uncinata of M. truncatula, of uncertain taxonomic status, has at least one M. turbinata allele. Both species can be differentiated by their specific allozymes. In general, the alleles of the isozymic loci segregated in a Mendelian fashion in the expected ratios for monomeric enzymes. The presence of chlorophyll-deficient plants on some of the progenies involving different taxonomic forms of the species M. turbinata indicates the presence of isolation barriers between these forms. The lack of segregation at locus Lap1-1 in the tetraploidized interspecific hybrid proves its alloploid nature.


1976 ◽  
Vol 28 (1) ◽  
pp. 27-36 ◽  
Author(s):  
Juhani Lokki ◽  
Anssi Saura ◽  
Pekka Lankinen ◽  
Esko Suomalainen

SUMMARYThe genetic variability at 16 enzyme loci in 52 Scandinavian triploid parthenogenetic populations of the beetle Adoxus obscurus has been studied by starch-gel electrophoresis. The overall genotypes of different beetles have been compared with each other and with a sample from a diploid bisexual population from Canada. Eighty per cent of the parthenogenetic beetles have the same overall genotype. The remainder belong to six genotypes, three of which are found in only one population. The variability within and between parthenogenetic populations of A. obscurus is much lower than in other comparable parthenogenetic insects studied by us. This is interpreted to be a consequence of the efficient migration of the genotypes with the highest fitness, leading to a replacement of less-adapted genotypes. A. obscurus is a flying insect, whereas the other parthenogenetic insects studied by us are sluggish flightless forms.



1988 ◽  
Vol 66 (3) ◽  
pp. 588-594 ◽  
Author(s):  
Hong Zhu ◽  
Kenneth O. Higginbotham ◽  
Bruce P. Dancik ◽  
Stan Navratil

Mycelial extracts of 43 isolates of Suillus tomentosus (Kauffm.) Singer, Snell & Dick collected from four boreal forest regions in Alberta were subjected to starch gel electrophoresis. A total of 21 bands was resolved from eight different enzyme systems presumably representing 13 loci. Six loci were polymorphic among these isolates. Cluster and principal components analyses demonstrated that intraspecific genetic variability of this fungus existed among and within forest regions. Polymorphic loci of acid phosphatase and alkaline phosphatase exhibited the greatest genetic similarity among the isolates within forest regions. Habitat isolation and host selection could be the major sources of genetic variation among forest regions.



1977 ◽  
Vol 17 (89) ◽  
pp. 1020 ◽  
Author(s):  
J McCausland ◽  
CW Wrigley

A range of laboratory methods was examined for their ability to distinguish between 19 barley cultivars currently grown in Australia. Aleurone colour, revealed after mechanical or chemical dehulling, differentiated Abyssinian, Atlas, Cape and Corvette from the other cultivars. Peroxidase and phenol testing were not useful. Seven different patterns were obtained for the hordeins of lowest mobility by starch gel electrophoresis. Further distinction was provided by flat gel isoelectric focusing of the water-soluble and hordein proteins for which 13 different pattern-groupings were obtained. The two electrophoretic techniques complemented one another, so that the use of both methods left only a few cultivars that could not be distinguished.



Weed Science ◽  
1995 ◽  
Vol 43 (1) ◽  
pp. 156-162 ◽  
Author(s):  
Yanglin Hou ◽  
Tracy M. Sterling

Broom snakeweed, a perennial rangeland shrub, is highly variable morphologically and can grow under a broad range of environmental conditions. In this study, isozyme analysis using starch gel electrophoresis was used to quantify genetic variability within and among New Mexico populations of broom snakeweed. Eight separate populations of broom snakeweed and one population of threadleaf snakeweed as a comparison were investigated. of the 10 enzyme systems examined, 16 loci were identified in eight populations and two species. Eleven loci were monomorphic in eight populations and two species and five loci were polymorphic in at least one population or species. Genetic variability was large in broom and threadleaf snakeweed populations as determined by isozyme analysis. Genetic variability among broom snakeweed populations was greater than that within populations for the five polymorphic loci. Cluster analysis of genetic distance and identity for the eight populations and two species characterized two major groups. Within broom snakeweed, cluster analysis characterized five groups. The two species shared most common alleles. The genetic variation identified in this research may account for the morphological differences and broad geographical distribution of broom snakeweed.



1971 ◽  
Vol 122 (5) ◽  
pp. 641-645 ◽  
Author(s):  
D. G. Taylor ◽  
R. G. Price ◽  
D. Robinson

1. A collagenase digest of rat kidney cortex was separated into four bands by zonal centrifugation. 2. Two of these bands were shown by light-microscopy to contain glomeruli and tubular fragments, which were free from each other and well separated from other renal material. 3. Protein, N-acetyl-β-glucosaminidase, 5′-nucleotidase, l-leucine β-naphthylamidase, leucine aminopeptidase, acid phosphatase and alkaline phosphatase were assayed across the gradient. 4. The greater proportion of these enzyme activities was recovered in the tubular fragments and acid phosphatase was the only enzyme detected in significant amounts in the glomeruli. 5. Tubular fragments and glomeruli were sedimented and multiple forms of β-naphthylamidase, N-acetyl-β-glucosaminidase, acid phosphatase and alkaline phosphatase were investigated by starch-gel electrophoresis.



1966 ◽  
Vol 44 (10) ◽  
pp. 1357-1364 ◽  
Author(s):  
Shun-Fong Hui ◽  
R. H. Common

Starch-gel electrophoresis of the total livetins of hen's egg yolk resolved 16 zones: seven major zones, six minor zones, and three faint, diffuse zones. One zone was identified with the major component of paper electrophoretic alpha-livetin and hence with serum albumin. Four of the major zones were identified with the major components of paper electrophoretic beta-livetin on the one hand, and with an electrophoretically heterogeneous livetin antigen (livetin antigen 3) on the other hand, thus establishing the electrophoretic heterogeneity and relative immunological homogeneity of the paper electrophoretic beta-livetin fraction. The other two major starch-gel electrophoretic zones were identified as transferrins by their positive staining reaction for iron and comparison of their mobilities with two corresponding serum starch-gel fractions.



1995 ◽  
Vol 120 (2) ◽  
pp. 318-324 ◽  
Author(s):  
Isabel Trujillo ◽  
Luis Rallo ◽  
Pere Arús

Pollen samples of 155 olive (Olea europaea L.) cultivars from different origins were analyzed to study isoenzymatic variability in five enzyme systems: alcohol dehydrogenase (ADH), esterase (EST), glucose phosphate isomerase (GPI), leucine aminopeptidase (LAP), and malic enzyme (ME) using starch gel electrophoresis. Polymorphism was observed in all of the isozyme systems. ME, GPI, EST, and LAP were the most useful systems for identification of cultivars. Different combinations of banding patterns of these systems allowed us to identify 85% of the cultivars. The remainder were separated into groups of two or three cultivars that could be identified using morphological characteristics. No intracultivar polymorphisms were observed.



1989 ◽  
Vol 46 (11) ◽  
pp. 1945-1951 ◽  
Author(s):  
Hiroaki Okamoto

Sand fance (Genus Ammodytes) collected from four stations off Japan and one station at Kodiak, Alaska were genetically characterized at 17 protein coding loci using starch-gel electrophoresis. Sand lance in Wakkanai (Cape Soya, Japan) consist of two genetically distinct groups. They are fixed for different alleles at four loci (Ldh-2, -3, G3pdh-2, and Mdhp-2). The genetic structure of one of the groups (Wakkanai-a group, W-a) is similar to that of A. personatus around Japan. The other group (Wakkanai-b group, W-b) has different genetic structure from either A. personatus or the Alaskan collection, which is presumed to belong to A. hexapterus. It is not presently possible to identify the affiliation of the W-b group; however, despite its sympatry with the W-a group, it is reproductively isolated and therefore is probably a distinct species occurring northeast of Hokkaido.



1977 ◽  
Vol 55 (4) ◽  
pp. 748-758 ◽  
Author(s):  
Charles F. Nadler ◽  
Robert S. Hoffmann

Serum transferrins and 11 other genetically controlled proteins representing 17 loci were examined by starch-gel electrophoresis from Siberian, Alaskan, and Canadian populations of Spermophilus parryii. Six transferrin alleles were identified. Arctic populations (S. p. parryii, S. p. osgoodi) were characterized by Tf 6 occurring alone or together with Tf 7 whereas middle and subarctic populations exhibited Tf 7 occurring either alone (S. p. ablusus, S. p. lyratus, S. p. plesius) or together with Tf 5 (S. p. plesius). Tf 8, Tf 9, and Tf 19 constituted local variants. Tf 6 displayed a clinal distribution, increasing in frequency eastward and paralleling a clinal increase in body size. Three PGM2 alleles were observed, the frequencies of which tend to differentiate arctic S. p. parryii from subarctic S. p. ablusus. G6PD-b occurred uniformly in North America and in one Siberian population; a second population (two specimens) exhibited G6PD-a, thereby suggesting that G6PD polymorphism may be present in Siberian S. parryii. The other nine proteins were monomorphic in all Holarctic populations.



1991 ◽  
Vol 69 (5) ◽  
pp. 1183-1188 ◽  
Author(s):  
Phyllis K. Kennedy ◽  
Michael L. Kennedy ◽  
Peter L. Clarkson ◽  
Ilme S. Liepins

The genetic variability of gray wolves (Canis lupus) from northwestern Canada was assessed through starch-gel electrophoresis. Of 27 protein systems examined, 25, representing 37 presumptive loci, were consistently scorable; 7 proteins (5 were consistently scorable) exhibited polymorphism. The level of heterozygosity (3.0%) was medial relative to values reported for natural populations of Carnivora and high relative to values reported for natural populations of canids. An overall pattern of few deviations from Hardy–Weinberg expectations and some spatial heterogeneity was observed. Wolves associated with different caribou herds exhibited a low level of differentiation (FST = 0.029). The pattern of variability supports the view of a large panmictic population resulting from extensive movements of individuals and packs and from natural and human impacts on pack structure and formation.



Sign in / Sign up

Export Citation Format

Share Document