The genetic basis of sexual isolation between Drosophila melanogaster and D. simulans
The genetic analysis of sexual isolation between the closely-related species Drosophila melanogaster and Drosophila simulans involved two experiments with no-choice tests. The efficiency of sexual isolation was measured by the frequency of courtship initiation and interspecific mating. We first surv...
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Published in: | Evolution Vol. 46; no. 5; pp. 1385 - 1398 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
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Malden, MA
Society for the Study of Evolution
01-10-1992
Blackwell Oxford University Press |
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Abstract | The genetic analysis of sexual isolation between the closely-related species Drosophila melanogaster and Drosophila simulans involved two experiments with no-choice tests. The efficiency of sexual isolation was measured by the frequency of courtship initiation and interspecific mating. We first surveyed the variation in sexual isolation between D. melanogaster strains and D. simulans strains of different geographic origin. Then, to investigate variation in sexual isolation within strains, we made F1diallel sets of reciprocal crosses within strains of D. melanogaster and D. simulans. The F1diallel progeny of one sex were paired with the opposite sex of the other species. The first experiment showed significant differences in the frequency of interspecific mating between geographic strains. There were more matings between D. simulans females and D. melanogaster males than between D. melanogaster females and D. simulans males. The second experiment uncovered that the male genotypes in the D. melanogaster diallel significantly differed in interspecific mating frequency, but not in courtship initiation frequency. The female genotypes in the D. simulans diallel were not significantly different in courtship initiation and interspecific mating frequency. Genetic analysis reveals that in D. melanogaster males sexual isolation was not affected by either maternal cytoplasmic effects, sex-linked effects, or epistatic interaction. The main genetic components were directional dommance and overdominance. The F1males achieved more matings with D. simulans females than the inbred males. The genetic architecture of sexual isolation in D. melanogaster males argues for a history of weak or no selection for lower interspecific mating propensity. The behavioral causes of variation in sexual isolation between the two species are discussed. |
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AbstractList | The genetic analysis of sexual isolation between the closely-related species Drosophila melanogaster and Drosophila simulans involved two experiments with no-choice tests. The efficiency of sexual isolation was measured by the frequency of courtship initiation and interspecific mating. We first surveyed the variation in sexual isolation between D. melanogaster strains and D. simulans strains of different geographic origin. Then, to investigate variation in sexual isolation within strains, we made F
diallel sets of reciprocal crosses within strains of D. melanogaster and D. simulans. The F
diallel progeny of one sex were paired with the opposite sex of the other species. The first experiment showed significant differences in the frequency of interspecific mating between geographic strains. There were more matings between D. simulans females and D. melanogaster males than between D. melanogaster females and D. simulans males. The second experiment uncovered that the male genotypes in the D. melanogaster diallel significantly differed in interspecific mating frequency, but not in courtship initiation frequency. The female genotypes in the D. simulans diallel were not significantly different in courtship initiation and interspecific mating frequency. Genetic analysis reveals that in D. melanogaster males sexual isolation was not affected by either maternal cytoplasmic effects, sex-linked effects, or epistatic interaction. The main genetic components were directional dominance and overdominance. The F
males achieved more matings with D. simulans females than the inbred males. The genetic architecture of sexual isolation in D. melanogaster males argues for a history of weak or no selection for lower interspecific mating propensity. The behavioral causes of variation in sexual isolation between the two species are discussed. The genetic analysis of sexual isolation between the closely-related species Drosophila melanogaster and Drosophila simulans involved two experiments with no-choice tests. The efficiency of sexual isolation was measured by the frequency of courtship initiation and interspecific mating. We surveyed the variation in sexual isolation between D. melanogaster strains and D. simulans strains of different geographic origin. Then, to investigate variation in sexual isolation within strains, we made F sub(1) diallel sets of reciprocal crosses within strains of D. melanogaster) and D. simulans . The F sub(1) diallel progeny of one sex were paired with the opposite sex of the other species. The first experiment showed significant differences in the frequency of interspecific mating between geographic strains. Genetic analysis reveals that in D. melanogaster) males sexual isolation was not affected by either maternal cytoplasmic effects, sex-linked effects, or epistatic interaction. The main genetic components were directional dominance and overdominance. The F sub(1) males achieved more matings with D. simulans) females than the inbred males. The genetic architecture of sexual isolation in D. melanogaster males argues for a history of weak or no selection for lower interspecific mating propensity. The behavioral causes of variation in sexual isolation between the two species are discussed. The genetic analysis of sexual isolation between the closely-related species Drosophila melanogaster and Drosophila simulans involved two experiments with no-choice tests. The efficiency of sexual isolation was measured by the frequency of courtship initiation and interspecific mating. We first surveyed the variation in sexual isolation between D. melanogaster strains and D. simulans strains of different geographic origin. Then, to investigate variation in sexual isolation within strains, we made F1 diallel sets of reciprocal crosses within strains of D. melanogaster and D. simulans. The F1 diallel progeny of one sex were paired with the opposite sex of the other species. The first experiment showed significant differences in the frequency of interspecific mating between geographic strains. There were more matings between D. simulans females and D. melanogaster males than between D. melanogaster females and D. simulans males. The second experiment uncovered that the male genotypes in the D. melanogaster diallel significantly differed in interspecific mating frequency, but not in courtship initiation frequency. The female genotypes in the D. simulans diallel were not significantly different in courtship initiation and interspecific mating frequency. Genetic analysis reveals that in D. melanogaster males sexual isolation was not affected by either maternal cytoplasmic effects, sex-linked effects, or epistatic interaction. The main genetic components were directional dominance and overdominance. The F1 males achieved more matings with D. simulans females than the inbred males. The genetic architecture of sexual isolation in D. melanogaster males argues for a history of weak or no selection for lower interspecific mating propensity. The behavioral causes of variation in sexual isolation between the two species are discussed. The genetic analysis of sexual isolation between the closely-related species Drosophila melanogaster and Drosophila simulans involved two experiments with no-choice tests. The efficiency of sexual isolation was measured by the frequency of courtship initiation and interspecific mating. We first surveyed the variation in sexual isolation between D. melanogaster strains and D. simulans strains of different geographic origin. Then, to investigate variation in sexual isolation within strains, we made F1diallel sets of reciprocal crosses within strains of D. melanogaster and D. simulans. The F1diallel progeny of one sex were paired with the opposite sex of the other species. The first experiment showed significant differences in the frequency of interspecific mating between geographic strains. There were more matings between D. simulans females and D. melanogaster males than between D. melanogaster females and D. simulans males. The second experiment uncovered that the male genotypes in the D. melanogaster diallel significantly differed in interspecific mating frequency, but not in courtship initiation frequency. The female genotypes in the D. simulans diallel were not significantly different in courtship initiation and interspecific mating frequency. Genetic analysis reveals that in D. melanogaster males sexual isolation was not affected by either maternal cytoplasmic effects, sex-linked effects, or epistatic interaction. The main genetic components were directional dommance and overdominance. The F1males achieved more matings with D. simulans females than the inbred males. The genetic architecture of sexual isolation in D. melanogaster males argues for a history of weak or no selection for lower interspecific mating propensity. The behavioral causes of variation in sexual isolation between the two species are discussed. Utilizing two experiments with no-choice tests, a genetic analysis of sexual isolation between the close-related species Drosophila melanogaster and Drosophila simulans is presented. The behavioral causes of variation in sexual isolation between the two species are discussed. |
Author | Scharloo W Kohler W Welbergen P Dijken F.R. van |
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CitedBy_id | crossref_primary_10_1038_hdy_1995_78 crossref_primary_10_1038_hdy_1994_64 crossref_primary_10_1007_BF01955171 crossref_primary_10_1046_j_1365_2540_1998_00317_x crossref_primary_10_1093_genetics_iyae039 crossref_primary_10_1038_sj_hdy_6882560 |
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Issue | 5 |
Keywords | Drosophila simulans Reproductive isolation Genetic variability Arthropoda Insecta Sexual behavior Interspecific hybridization Diallel analysis Invertebrata Drosophila melanogaster Diptera Drosophilidae intraspecific variability Biometric genetics Drosophila sexual isolation |
Language | English |
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61 Ehrman (10.1111/j.1558-5646.1992.tb01131.x-BIB0025|evo01131-cit-0025) 1961; 46 Mayr (10.1111/j.1558-5646.1992.tb01131.x-BIB0059|evo01131-cit-0059) 1959; 103 Thornhill (10.1111/j.1558-5646.1992.tb01131.x-BIB0083|evo01131-cit-0083) 1983 Fisher (10.1111/j.1558-5646.1992.tb01131.x-BIB0030|evo01131-cit-0030) 1930 Hayman (10.1111/j.1558-5646.1992.tb01131.x-BIB0036|evo01131-cit-0036) 1954a; 10 Mather (10.1111/j.1558-5646.1992.tb01131.x-BIB0056|evo01131-cit-0056) 1982 Mather (10.1111/j.1558-5646.1992.tb01131.x-BIB0055|evo01131-cit-0055) 1966; 164 Crusio (10.1111/j.1558-5646.1992.tb01131.x-BIB0023|evo01131-cit-0023) 1984; 14 Grula (10.1111/j.1558-5646.1992.tb01131.x-BIB0034|evo01131-cit-0034) 1980; 34 Ronen (10.1111/j.1558-5646.1992.tb01131.x-BIB0075|evo01131-cit-0075) 1957; 31 Collins (10.1111/j.1558-5646.1992.tb01131.x-BIB0018|evo01131-cit-0018) 1984; 53 Hadorn (10.1111/j.1558-5646.1992.tb01131.x-BIB0035|evo01131-cit-0035) 1961; 68 Sturtevant (10.1111/j.1558-5646.1992.tb01131.x-BIB0079|evo01131-cit-0079) 1920; 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2 Fulker (10.1111/j.1558-5646.1992.tb01131.x-BIB0031|evo01131-cit-0031) 1966; 153 Carson (10.1111/j.1558-5646.1992.tb01131.x-BIB0015|evo01131-cit-0015) 1975; 109 Lande (10.1111/j.1558-5646.1992.tb01131.x-BIB0047|evo01131-cit-0047) 1981; 78 Hayman (10.1111/j.1558-5646.1992.tb01131.x-BIB0037|evo01131-cit-0037) 1954b; 39 Barker (10.1111/j.1558-5646.1992.tb01131.x-BIB0003|evo01131-cit-0003) 1967; 101 Sperlich (10.1111/j.1558-5646.1992.tb01131.x-BIB0077|evo01131-cit-0077) 1962; 36 Kamping (10.1111/j.1558-5646.1992.tb01131.x-BIB0042|evo01131-cit-0042) 1991; 70 Lande (10.1111/j.1558-5646.1992.tb01131.x-BIB0050|evo01131-cit-0050) 1985 Markow (10.1111/j.1558-5646.1992.tb01131.x-BIB0053|evo01131-cit-0053) 1987; 84 Futch (10.1111/j.1558-5646.1992.tb01131.x-BIB0032|evo01131-cit-0032) 1973; 27 Endler (10.1111/j.1558-5646.1992.tb01131.x-BIB0026|evo01131-cit-0026) 1989 Walters (10.1111/j.1558-5646.1992.tb01131.x-BIB0084|evo01131-cit-0084) 1977; 38 Mayr (10.1111/j.1558-5646.1992.tb01131.x-BIB0065|evo01131-cit-0065) 1942; 6 Eoff (10.1111/j.1558-5646.1992.tb01131.x-BIB0027|evo01131-cit-0027) 1975; 109 Mayr (10.1111/j.1558-5646.1992.tb01131.x-BIB0061|evo01131-cit-0061) 1982 Biddle (10.1111/j.1558-5646.1992.tb01131.x-BIB0005|evo01131-cit-0005) 1932; 17 Carracedo (10.1111/j.1558-5646.1992.tb01131.x-BIB0013|evo01131-cit-0013) 1989; 80 Sturtevant (10.1111/j.1558-5646.1992.tb01131.x-BIB0080|evo01131-cit-0080) 1929; 399 Mayr (10.1111/j.1558-5646.1992.tb01131.x-BIB0069|evo01131-cit-0069) 1982; 78 Muller (10.1111/j.1558-5646.1992.tb01131.x-BIB0064|evo01131-cit-0064) 1940 Welbergen (10.1111/j.1558-5646.1992.tb01131.x-BIB0089|evo01131-cit-0089) 1992; 5 Coyne (10.1111/j.1558-5646.1992.tb01131.x-BIB0022|evo01131-cit-0022) 1989; 86 Price (10.1111/j.1558-5646.1992.tb01131.x-BIB0070|evo01131-cit-0070) 1987 Cobb (10.1111/j.1558-5646.1992.tb01131.x-BIB0017|evo01131-cit-0017) 1986; 97 Hotta (10.1111/j.1558-5646.1992.tb01131.x-BIB0039|evo01131-cit-0039) 1976; 73 Liimatainen (10.1111/j.1558-5646.1992.tb01131.x-BIB0051|evo01131-cit-0051) 1992; 43 Ringo (10.1111/j.1558-5646.1992.tb01131.x-BIB0073|evo01131-cit-0073) 1987b; 17 Burnet (10.1111/j.1558-5646.1992.tb01131.x-BIB0008|evo01131-cit-0008) 1974 Robertson (10.1111/j.1558-5646.1992.tb01131.x-BIB0074|evo01131-cit-0074) 1983; 37 Mayr (10.1111/j.1558-5646.1992.tb01131.x-BIB0058|evo01131-cit-0058) 1954 Kessler (10.1111/j.1558-5646.1992.tb01131.x-BIB0045|evo01131-cit-0045) 1966; 20 Paterson (10.1111/j.1558-5646.1992.tb01131.x-BIB0068|evo01131-cit-0068) 1981; 77 Mayr (10.1111/j.1558-5646.1992.tb01131.x-BIB0067|evo01131-cit-0067) 1974; 4 Welbergen (10.1111/j.1558-5646.1992.tb01131.x-BIB0088|evo01131-cit-0088) 1987; 101 Mayr (10.1111/j.1558-5646.1992.tb01131.x-BIB0060|evo01131-cit-0060) 1963 Connolly (10.1111/j.1558-5646.1992.tb01131.x-BIB0020|evo01131-cit-0020) 1973; 44 Inoue (10.1111/j.1558-5646.1992.tb01131.x-BIB0040|evo01131-cit-0040) 1990; 65 Parsons (10.1111/j.1558-5646.1992.tb01131.x-BIB0066|evo01131-cit-0066) 1972; 14 Ringo (10.1111/j.1558-5646.1992.tb01131.x-BIB0071|evo01131-cit-0071) 1986; 97 Kamping (10.1111/j.1558-5646.1992.tb01131.x-BIB0041|evo01131-cit-0041) 1988; 67 Connolly (10.1111/j.1558-5646.1992.tb01131.x-BIB0021|evo01131-cit-0021) 1974; 48 Barker (10.1111/j.1558-5646.1992.tb01131.x-BIB0002|evo01131-cit-0002) 1962; 96 Futuyma (10.1111/j.1558-5646.1992.tb01131.x-BIB0033|evo01131-cit-0033) 1986 Eoff (10.1111/j.1558-5646.1992.tb01131.x-BIB0028|evo01131-cit-0028) 1977; 111 Kawanishi (10.1111/j.1558-5646.1992.tb01131.x-BIB0044|evo01131-cit-0044) 1981; 35 Lande (10.1111/j.1558-5646.1992.tb01131.x-BIB0048|evo01131-cit-0048) 1982; 36 Butlin (10.1111/j.1558-5646.1992.tb01131.x-BIB0010|evo01131-cit-0010) 1989 Lewontin (10.1111/j.1558-5646.1992.tb01131.x-BIB0049|evo01131-cit-0049) 1974 Mayr (10.1111/j.1558-5646.1992.tb01131.x-BIB0057|evo01131-cit-0057) 1942 Mayr (10.1111/j.1558-5646.1992.tb01131.x-BIB0062|evo01131-cit-0062) 1988 |
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Snippet | The genetic analysis of sexual isolation between the closely-related species Drosophila melanogaster and Drosophila simulans involved two experiments with... The genetic analysis of sexual isolation between the closely‐related species Drosophila melanogaster and Drosophila simulans involved two experiments with... Utilizing two experiments with no-choice tests, a genetic analysis of sexual isolation between the close-related species Drosophila melanogaster and Drosophila... |
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SubjectTerms | Animals Biological and medical sciences Biometric genetics Classical genetics, quantitative genetics, hybrids Drosophila Drosophila melanogaster Drosophila simulans Evolutionary genetics Female animals Fundamental and applied biological sciences. Psychology genetic variation genetica Genetics Genetics of eukaryotes. Biological and molecular evolution genetique Genotypes Hybridity Inbred strains Insect genetics Insects intraspecific variability Invertebrata Male animals Mating behavior Quantitative genetics Sexual behavior sexual isolation variacion genetica variation genetique |
Title | The genetic basis of sexual isolation between Drosophila melanogaster and D. simulans |
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