2018
DOI: 10.1371/journal.pgen.1007686
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Genetic basis of thermal plasticity variation in Drosophila melanogaster body size

Abstract: Body size is a quantitative trait that is closely associated to fitness and under the control of both genetic and environmental factors. While developmental plasticity for this and other traits is heritable and under selection, little is known about the genetic basis for variation in plasticity that can provide the raw material for its evolution. We quantified genetic variation for body size plasticity in Drosophila melanogaster by measuring thorax and abdomen length of females reared at two temperatures from … Show more

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Cited by 62 publications
(120 citation statements)
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“…To isolate the two alternative foxo alleles for experiments, we used whole-genome sequenced inbred lines from the Drosophila Genetic Reference Panel (DGRP; Mackay et al 2012) to reconstitute outbred populations either fixed for the LL (G,G) and the HL (A,T) alleles. This "reconstituted or recombinant outbred population" (ROP) or "Mendelian randomization" approach produces populations that are consistently and completely fixed for the two alternative allelic states to be compared, with the rest of the genetic background being randomized (see Behrman et al [2018] and Lafuente et al [2018] for examples using this method). For each allele, we used two independent sets of DGRP lines (sets A and B for HL; sets C and D for LL; each set consisting of 20 distinct lines) and two replicate population cages per set, giving a total of eight population cages ( Fig.…”
Section: Polymorphismmentioning
confidence: 99%
“…To isolate the two alternative foxo alleles for experiments, we used whole-genome sequenced inbred lines from the Drosophila Genetic Reference Panel (DGRP; Mackay et al 2012) to reconstitute outbred populations either fixed for the LL (G,G) and the HL (A,T) alleles. This "reconstituted or recombinant outbred population" (ROP) or "Mendelian randomization" approach produces populations that are consistently and completely fixed for the two alternative allelic states to be compared, with the rest of the genetic background being randomized (see Behrman et al [2018] and Lafuente et al [2018] for examples using this method). For each allele, we used two independent sets of DGRP lines (sets A and B for HL; sets C and D for LL; each set consisting of 20 distinct lines) and two replicate population cages per set, giving a total of eight population cages ( Fig.…”
Section: Polymorphismmentioning
confidence: 99%
“…The reasons for the observed thermal plasticity in size, and its potential adaptive value, remain poorly understood [19][20][21][22][23]. However, if smaller body size has fitness advantages at higher temperatures, temperature-size plasticity may represent adaptive variation [22,[24][25][26][27][28]. As a result, in general, it follows that for both endotherms and ectotherms that thermal plasticity in body size may be adaptive if smaller size is favoured at warmer temperatures.…”
Section: Introductionmentioning
confidence: 99%
“…Such intraspecific variation, or in this case variation within the meta-population, for plasticity is common in both natural and laboratory populations [e.g. 20, 62] and hypothesised to be beneficial for insects exposed to climate change [63, 64] because it increases their evolutionary potential [24].…”
Section: Discussionmentioning
confidence: 99%
“…For example, Singh et al showed that poor host plant quality mainly influenced development at intermediate temperatures the tropical butterfly Bicyclus anynana [18]. Moreover, significant genetic variation for (multidimensional) plasticity is known to exist in both natural and laboratory populations [20-22]. This intraspecific variation in the ability to respond to an environmental cue (GxE), or combinations of cues (GxExE), is hypothesised to be beneficial in the light of climate change since it facilitates the evolution of wider ranges of environmental tolerance [23, 24].…”
Section: Introductionmentioning
confidence: 99%