scholarly journals CONDITIONAL POLYGENIC EFFECTS IN THE STERNOPLEURAL BRISTLE SYSTEM OF DROSOPHILA MELANOGASTER

Genetics ◽  
1984 ◽  
Vol 108 (2) ◽  
pp. 409-424
Author(s):  
Fred B Schnee ◽  
James N Thompson
Keyword(s):  
Drosophila Melanogaster ◽  
Environment Interaction ◽  
Temperature Dependent ◽  
Genotype Environment Interaction ◽  
Bristle Number ◽  
The Face ◽  
Chromosomal Architecture ◽  
Selection For ◽  
Response To Temperature ◽  
Polygenic Variation

ABSTRACT The chromosomal architecture of genotype × environment interactions was investigated in lines of Drosophila melanogaster selected for increased or decreased sternopleural bristle number at 18°, 25° and 29°. In general, interactions were found to have a stabilizing effect upon the bristle phenotype, in the sense that the genotype × environment interaction tended to increase bristle number under conditions in which temperature alone reduced bristle number and vice versa. The polygenic modifiers of mean bristle number were often separable from modifiers of the response to temperature both at the chromosomal level and intrachromosomally. In one of the low selection lines, a temperature-dependent polygenic locus was mapped on chromosome 3. It is suggested that genotype × environment interactions be thought of in terms of conditional polygenic expression. Such conditionality may be one of the ways in which polygenic variation is maintained in a population in the face of selection for an optimum phenotype.

scholarly journals Temporal uniformity of the spontaneous mutational variance of quantitative traits in Drosophila melanogaster

2000 ◽  
Vol 75 (1) ◽  
pp. 47-51 ◽  
Author(s):  
AURORA GARCÍA-DORADO ◽  
JESUS FERNÁNDEZ ◽  
CARLOS LÓPEZ-FANJUL
Keyword(s):  
Drosophila Melanogaster ◽  
Morphological Traits ◽  
Quantitative Traits ◽  
Wing Length ◽  
Environment Interaction ◽  
Genotype Environment Interaction ◽  
Bristle Number ◽  
Sib Mating ◽  
Mutational Variance ◽  
Interaction Variance

Spontaneous mutations were allowed to accumulate over 209 generations in more than 100 lines, all of them independently derived from a completely homozygous population of Drosophila melanogaster and subsequently maintained under strong inbreeding (equivalent to full-sib mating). Traits scored were: abdominal (AB) and sternopleural (ST) bristle number, wing length (WL) and egg-to-adult viability (V). On two occasions – early (generations 93–122) and late (generations 169–209) – ANOVA estimates of the mutational variance and the mutational line × generation interaction variance were obtained. Mutational heritabilities of morphological traits ranged from 2 × 10−4 to 2 × 10−3 and the mutational coefficient of variation of viability was 0·01. For AB, WL and V, temporal uniformity of the mutational variance was observed. However, a fluctuation of the mutational heritability of ST was detected and could be ascribed to random genotype × environment interaction.

scholarly journals Genotype-Environment Interaction at Quantitative Trait Loci Affecting Sensory Bristle Number in Drosophila melanogaster

Genetics ◽  
1998 ◽  
Vol 149 (4) ◽  
pp. 1883-1898 ◽  
Author(s):  
Marjorie C Gurganus ◽  
James D Fry ◽  
Sergey V Nuzhdin ◽  
Elena G Pasyukova ◽  
Richard F Lyman ◽  
...  
Keyword(s):  
Drosophila Melanogaster ◽  
Quantitative Trait Loci ◽  
Quantitative Trait ◽  
Rank Order ◽  
Recombinant Inbred Lines ◽  
Environment Interaction ◽  
Genotype Environment Interaction ◽  
Bristle Number ◽  
A Genome ◽  
Trait Loci

AbstractThe magnitude of segregating variation for bristle number in Drosophila melanogaster exceeds that predicted from models of mutation-selection balance. To evaluate the hypothesis that genotype-environment interaction (GEI) maintains variation for bristle number in nature, we quantified the extent of GEI for abdominal and sternopleural bristles among 98 recombinant inbred lines, derived from two homozygous laboratory strains, in three temperature environments. There was considerable GEI for both bristle traits, which was mainly attributable to changes in rank order of line means. We conducted a genome-wide screen for quantitative trait loci (QTLs) affecting bristle number in each sex and temperature environment, using a dense (3.2-cM) marker map of polymorphic insertion sites of roo transposable elements. Nine sternopleural and 11 abdominal bristle number QTLs were detected. Significant GEI was exhibited by 14 QTLs, but there was heterogeneity among QTLs in their sensitivity to thermal and sexual environments. To further evaluate the hypothesis that GEI maintains variation for bristle number, we require estimates of allelic effects across environments at genetic loci affecting the traits. This level of resolution may be achievable for Drosophila bristle number because candidate loci affecting bristle development often map to the same location as bristle number QTLs.

scholarly journals Hybrid dysgenesis-induced quantitative variation on the X chromosome of Drosophila melanogaster.

Genetics ◽  
1990 ◽  
Vol 124 (3) ◽  
pp. 627-636
Author(s):  
C Q Lai ◽  
T F Mackay
Keyword(s):  
Drosophila Melanogaster ◽  
X Chromosome ◽  
Quantitative Traits ◽  
Natural Populations ◽  
Quantitative Variation ◽  
Hybrid Dysgenesis ◽  
X Chromosomes ◽  
Bristle Number ◽  
Seven Generations ◽  
Polygenic Variation

Abstract To determine the ability of the P-M hybrid dysgenesis system of Drosophila melanogaster to generate mutations affecting quantitative traits, X chromosome lines were constructed in which replicates of isogenic M and P strain X chromosomes were exposed to a dysgenic cross, a nondysgenic cross, or a control cross, and recovered in common autosomal backgrounds. Mutational heritabilities of abdominal and sternopleural bristle score were in general exceptionally high-of the same magnitude as heritabilities of these traits in natural populations. P strain chromosomes were eight times more mutable than M strain chromosomes, and dysgenic crosses three times more effective than nondysgenic crosses in inducing polygenic variation. However, mutational heritabilities of the bristle traits were appreciable for P strain chromosomes passed through one nondysgenic cross, and for M strain chromosomes backcrossed for seven generations to inbred P strain females, a result consistent with previous observations on mutations affecting quantitative traits arising from nondysgenic crosses. The new variation resulting from one generation of mutagenesis was caused by a few lines with large effects on bristle score, and all mutations reduced bristle number.

scholarly journals Experimental modification of the dominance relations of a melanotic tumour gene in Drosophila melanogaster

1972 ◽  
Vol 20 (1) ◽  
pp. 115-135 ◽  
Author(s):  
Ann Louise Belt ◽  
Barrie Burnet
Keyword(s):  
Drosophila Melanogaster ◽  
Larval Instar ◽  
Environment Interaction ◽  
Larval Food ◽  
Dominance Relations ◽  
The Third ◽  
Genotype Environment Interaction ◽  
Tumour Formation ◽  
Food Medium ◽  
Melanotic Tumour

SUMMARYThe melanotic tumour gene tu-C4 in Drosophila melanogaster shows incomplete dominance, together with variable penetrance and expressivity. It is tentatively located in the region of locus 52–53 on the third chromosome. Tumour formation in mutant homozygotes involves a precocious haemocyte transformation leading to the appearance of lamellocytes at the beginning of the third larval instar. These aggregate to form tumour-like masses which subsequently melanize. The process of tumour formation is in broad outline similar to that found in other tumour strains. Melanotic tumour formation is treated as a dichotomous threshold character, assuming an underlying normal distribution of liability relative to a fixed threshold. The expression of the tumour gene can be influenced by the levels of protein, phospholipid, nucleic acid and carbohydrate in the larval food medium, and changes in dominance and penetrance induced by sub-optimal environments deficient in these nutrients are positively correlated. Reinforcement by selection of the dominance relations of tu-C4 was accompanied by correlated changes in penetrance. Conversely, selection for increased penetrance was accompanied by correlated changes in dominance. Dominance and penetrance, it is concluded, are fundamentally related aspects of tumour gene expression. Recruitment of dominance modifiers linked to the tumour gene was excluded by the mating scheme employed, and the observed changes in dominance relations in response to selection were due largely to modifiers located on the second chromosome. Changes in dominance relations produced by selection could be significantly reinforced, or reversed, by environmental factors and consequently show a substantial genotype – environment interaction effect. These facts are relevant to current theories of dominance evolution.

scholarly journals Challenges and adaptive strategies in pig breeding from the aspect of heat stress and heat tolerance

2020 ◽  
Vol 24 (1) ◽  
pp. 1-13
Author(s):  
István Nagy ◽  
György Kövér ◽  
Zsolt Gerencsér ◽  
Gabriella Szász
Keyword(s):  
Heat Tolerance ◽  
Temperature Effects ◽  
Selection Criteria ◽  
Relevant Literature ◽  
Genetic Selection ◽  
Adaptive Strategies ◽  
Environment Interaction ◽  
Genotype Environment Interaction ◽  
Selection For ◽  
The Ideal

Authors summarized the results of the last three decades’ relevant literature examining the temperature effects on the various growth, reproductive and carcass traits in pigs. The ideal period of temperature measurement and the different methodologies characterizing temperature effects were summarized. The aspects of genotype environment interaction for the measured traits under hot and temperate conditions were also presented. Finally the possibilities of direct genetic selection for heat tolerance and its possible selection criteria traits were also discussed.

scholarly journals Studies on The Scutellar Bristles of Drosophila Melanogaster I. Basic Variability, Some Temperature and Culture Effects, and Responses to Short-Term Selection in the Oregon-Rc Strain

1968 ◽  
Vol 21 (4) ◽  
pp. 721 ◽  
Author(s):  
BL Sheldon
Keyword(s):  
Drosophila Melanogaster ◽  
Major Gene ◽  
Selection Response ◽  
Wild Type ◽  
Short Term ◽  
Term Selection ◽  
Bristle Number ◽  
Selection For ◽  
High Selection ◽  
Culture Effects

The results of short runs of disruptive and high selection for scutellar bristles in wild-type Drosophila are explained in terms of the hypothesis that canalization at four bristles is due to regulation of the major gene in the developmental system (Rendel, Sheldon, and Finlay 1965). Selection response has probably been due to selection for modifier (minor) genes rather than for isoalleles of the major gene or weak regulator alleles. Some environmental effects on the character, short runs of selection for low bristle number or different bristle types, and effects of relaxing selection are also reported.

scholarly journals Long-term selection for a quantitative character in large replicate populations of Drosophila melanogaster: 1. Response to selection

1980 ◽  
Vol 35 (1) ◽  
pp. 1-17 ◽  
Author(s):  
B. H. Yoo
Keyword(s):  
Drosophila Melanogaster ◽  
Phenotypic Variability ◽  
Selection Response ◽  
Quantitative Character ◽  
Response Patterns ◽  
Total Response ◽  
Term Selection ◽  
Bristle Number ◽  
Selection For

SUMMARYThe response to long-term selection for increased abdominal bristle number was studied in six replicate lines of Drosophila melanogaster derived from the sc Canberra outbred strain. Each line was continued for 86–89 generations with 50 pairs of parents selected at an intensity of 20%, and subsequently for 32–35 generations without selection. Response continued for at least 75 generations and average total response was in excess of 36 additive genetic standard deviations of the base population (σA) or 51 times the response in the first generation. The pattern of longterm response was diverse and unpredictable typically with one or more accelerated responses in later generations. At termination of the selection, most of the replicate lines were extremely unstable with high phenotypic variability, and lost much of their genetic gains rapidly upon relaxation of selection.The variation in response among replicates rose in the early phase of selection to level off at approximately 7·6 around generation 25. As some lines plateaued, it increased further to a level higher than would be accommodated by most genetic models. The replicate variation was even higher after many generations of relaxed selection. The genetic diversity among replicates, as revealed in total response, the individuality of response patterns and variation of the sex-dimorphism ratio, suggests that abdominal bristle number is influenced potentially by a large number of genes, but a smaller subset of them was responsible for selection response in any one line.

Sign in / Sign up

Export Citation Format

Share Document