2015
DOI: 10.1534/genetics.115.175489
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Dominance Genetic Variance for Traits Under Directional Selection inDrosophila serrata

Abstract: In contrast to our growing understanding of patterns of additive genetic variance in single-and multi-trait combinations, the relative contribution of nonadditive genetic variance, particularly dominance variance, to multivariate phenotypes is largely unknown. While mechanisms for the evolution of dominance genetic variance have been, and to some degree remain, subject to debate, the pervasiveness of dominance is widely recognized and may play a key role in several evolutionary processes. Theoretical and empir… Show more

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Cited by 22 publications
(46 citation statements)
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“…These results suggest that wing‐shape should be able to respond to selection in any direction in both sexes. They are consistent with an analysis of this population that found significant genetic variation in all directions of phenotype space when the male and female data were pooled (Houle and Meyer ), and with wing‐shape analyses of male Drosophila serrata (Sztepanacz and Blows ). We compared the fit of the model that estimated G m to the fit of a model where the (co)variances of G m were constrained to equal the best estimate of G f , to determine whether G m and G f differed statistically from each other.…”
Section: Resultssupporting
confidence: 88%
“…These results suggest that wing‐shape should be able to respond to selection in any direction in both sexes. They are consistent with an analysis of this population that found significant genetic variation in all directions of phenotype space when the male and female data were pooled (Houle and Meyer ), and with wing‐shape analyses of male Drosophila serrata (Sztepanacz and Blows ). We compared the fit of the model that estimated G m to the fit of a model where the (co)variances of G m were constrained to equal the best estimate of G f , to determine whether G m and G f differed statistically from each other.…”
Section: Resultssupporting
confidence: 88%
“…Indeed, nonadditive genetic effects have been shown to contribute significantly to population differentiation in various aspects of life history and morphology (Roff & Emerson, 2006). In contrast, their contribution to traits of evolutionary interest, and fitness especially, within natural populations remains poorly understood (Sztepanacz & Blows, 2015). …”
Section: Introductionmentioning
confidence: 99%
“…Variation in larval density among vials could potentially affect the phenotypic variance within families, and if density is largely determined by genetic variance in fitness, then this genetic variance in fitness can have a causal effect on phenotypic variance in wing phenotypes. A previous analysis of these wing data provides no evidence that common environment is an important component of the genetic variance in wings (Sztepanacz and Blows 2015), but the effect of common environment on micro-environmental variance is unknown. In total, we analyzed one wing from each of 5040 individuals in 685 families, and fitness from 2883 individuals in 666 families (Table 1).…”
Section: Methodsmentioning
confidence: 81%
“…The experimental design, based on a large, laboratory-adapted population of D. serrata housed under standard conditions at 25° (Hine et al 2014), is described in detail in Sztepanacz and Blows (2015). Briefly, the first generation employed a paternal-half-sibling breeding design, where 75 sires were each mated to three virgin dams (total of 225 dams).…”
Section: Methodsmentioning
confidence: 99%
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