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1.
Am Nat ; 196(5): 620-633, 2020 11.
Article in English | MEDLINE | ID: mdl-33064591

ABSTRACT

AbstractWhen populations evolve adaptive reaction norms in response to novel environments, it can occur through a process termed genetic accommodation. Under this model, the initial response to the environment is widely variable between genotypes as a result of cryptic genetic variation, which is then refined by selection to a single adaptive response. Here, I empirically test these predictions from genetic accommodation by measuring reaction norms in individual genotypes and across several time points. I compare two species of Drosophila that differ in their adaptation to ethanol (D. melanogaster and D. simulans). Both species are human commensals with a recent cosmopolitan expansion, but only D. melanogaster is adapted to ethanol exposure. Using gene expression as a phenotype and an approach that combines information about expression and alternative splicing, I find that D. simulans exhibits cryptic genetic variation in the response to ethanol, while D. melanogaster has almost no genotype-specific variation in reaction norm. This is evidence for adaptation to ethanol through genetic accommodation, suggesting that the evolution of phenotypic plasticity could be an important contributor to the ability to exploit novel resources.


Subject(s)
Drosophila melanogaster/genetics , Drosophila simulans/genetics , Ethanol/pharmacology , Adaptation, Physiological/genetics , Animals , Biological Evolution , Drosophila melanogaster/drug effects , Drosophila simulans/drug effects , Exons , Female , Gene Expression , Male , Sequence Analysis, RNA
4.
Elife ; 82019 10 15.
Article in English | MEDLINE | ID: mdl-31612861

ABSTRACT

A new study upturns the long-held belief that the yellow gene determines sex-specific behaviors in fruit flies by acting in the brain.


Subject(s)
Drosophila Proteins , Drosophila , Animals , Drosophila melanogaster , Female , Male , Reproduction , Sexual Behavior, Animal
5.
Evol Dev ; 21(3): 157-171, 2019 05.
Article in English | MEDLINE | ID: mdl-30756455

ABSTRACT

Robustness in development allows for the accumulation of genetically based variation in expression. However, this variation is usually examined in response to large perturbations, and examination of this variation has been limited to being spatial, or quantitative, but because of technical restrictions not both. Here we bridge these gaps by investigating replicated quantitative spatial gene expression using rigorous statistical models, in different genotypes, sexes, and species (Drosophila melanogaster and D. simulans). Using this type of quantitative approach with molecular developmental data allows for comparison among conditions, such as different genetic backgrounds. We apply this approach to the morphogenetic furrow, a wave of differentiation that patterns the developing eye disc. Within the morphogenetic furrow, we focus on four genes, hairy, atonal, hedgehog, and Delta. Hybridization chain reaction quantitatively measures spatial gene expression, co-staining for all four genes simultaneously. We find considerable variation in the spatial expression pattern of these genes in the eye between species, genotypes, and sexes. We also find that there has been evolution of the regulatory relationship between these genes, and that their spatial interrelationships have evolved between species. This variation has no phenotypic effect, and could be buffered by network thresholds or compensation from other genes. Both of these mechanisms could potentially be contributing to long term developmental systems drift.


Subject(s)
Drosophila Proteins/metabolism , Drosophila melanogaster/embryology , Drosophila melanogaster/metabolism , Drosophila simulans/embryology , Eye/embryology , Gene Expression Regulation, Developmental , Animals , Body Patterning , Drosophila melanogaster/genetics , Drosophila simulans/genetics , Drosophila simulans/metabolism , Eye/metabolism , Female , Genotype , Larva , Male , Models, Biological , Transcriptome
6.
Trends Genet ; 34(7): 532-544, 2018 07.
Article in English | MEDLINE | ID: mdl-29680748

ABSTRACT

There is abundant variation in gene expression between individuals, populations, and species. The evolution of gene regulation and expression within and between species is thought to frequently contribute to adaptation. Yet considerable evidence suggests that the primary evolutionary force acting on variation in gene expression is stabilizing selection. We review here the results of recent studies characterizing the evolution of gene expression occurring in cis (via linked polymorphisms) or in trans (through diffusible products of other genes) and their contribution to adaptation and response to the environment. We review the evidence for buffering of variation in gene expression at the level of both transcription and translation, and the possible mechanisms for this buffering. Lastly, we summarize unresolved questions about the evolution of gene regulation.


Subject(s)
Gene Expression Regulation/genetics , Gene Expression/genetics , Polymorphism, Genetic/genetics , Animals , Evolution, Molecular , Humans
7.
Genome Biol Evol ; 10(1): 189-206, 2018 01 01.
Article in English | MEDLINE | ID: mdl-29228179

ABSTRACT

The rapidly expanding availability of large NGS data sets provides an opportunity to investigate population genetics at an unprecedented scale. Drosophila simulans is the sister species of the model organism Drosophila melanogaster, and is often presumed to share similar demographic history. However, previous population genetic and ecological work suggests very different signatures of selection and demography. Here, we sequence a new panel of 170 inbred genotypes of a North American population of D. simulans, a valuable complement to the DGRP and other D. melanogaster panels. We find some unexpected signatures of demography, in the form of excess intermediate frequency polymorphisms. Simulations suggest that this is possibly due to a recent population contraction and selection. We examine the outliers in the D. simulans genome determined by a haplotype test to attempt to parse the contribution of demography and selection to the patterns observed in this population. Untangling the relative contribution of demography and selection to genomic patterns of variation is challenging, however, it is clear that although D. melanogaster was thought to share demographic history with D. simulans different forces are at work in shaping genomic variation in this population of D. simulans.


Subject(s)
Drosophila simulans/genetics , Genetic Variation , Selection, Genetic , Animals , Drosophila melanogaster/genetics , Genetics, Population , Genomics , Genotype , Haplotypes , Polymorphism, Genetic , Species Specificity
8.
Ecol Evol ; 7(23): 10031-10041, 2017 12.
Article in English | MEDLINE | ID: mdl-29238534

ABSTRACT

Indirect genetic effects (IGEs) describe the effect of the genes of social partners on the phenotype of a focal individual. Here, we measure indirect genetic effects using the "coefficient of interaction" (Ψ) to test whether Ψ evolved between Drosophila melanogaster and D. simulans. We compare Ψ for locomotion between ethanol and nonethanol environments in both species, but only D. melanogaster utilizes ethanol ecologically. We find that while sexual dimorphism for locomotion has been reversed in D. simulans, there has been no evolution of social effects between these two species. What did evolve was the interaction between genotype-specific Ψ and the environment, as D. melanogaster varies unpredictably between environments and D. simulans does not. In this system, this suggests evolutionary lability of sexual dimorphism but a conservation of social effects, which brings forth interesting questions about the role of the social environment in sexual selection.

9.
Evolution ; 71(7): 1765-1775, 2017 Jul.
Article in English | MEDLINE | ID: mdl-28489252

ABSTRACT

Despite strong purifying or directional selection, variation is ubiquitous in populations. One mechanism for the maintenance of variation is indirect genetic effects (IGEs), as the fitness of a given genotype will depend somewhat on the genes of its social partners. IGEs describe the effect of genes in social partners on the expression of the phenotype of a focal individual. Here, we ask what effect IGEs, and variation in IGEs between abiotic environments, has on locomotion in Drosophila. This trait is known to be subject to intralocus sexually antagonistic selection. We estimate the coefficient of interaction, Ψ, using six inbred lines of Drosophila. We found that Ψ varied between abiotic environments, and that it may vary across among male genotypes in an abiotic environment specific manner. We also found evidence that social effects of males alter the value of a sexually dimorphic trait in females, highlighting an interesting avenue for future research into sexual antagonism. We conclude that IGEs are an important component of social and sexual interactions and that they vary between individuals and abiotic environments in complex ways, with the potential to promote the maintenance of phenotypic variation.


Subject(s)
Drosophila melanogaster/genetics , Genetic Variation , Locomotion , Social Behavior , Animals , Environment , Female , Genotype , Male , Phenotype , Sexual Behavior, Animal
10.
Curr Biol ; 26(18): 2423-2433, 2016 09 26.
Article in English | MEDLINE | ID: mdl-27546578

ABSTRACT

Convergent evolution provides a type of natural replication that can be exploited to understand the roles of contingency and constraint in the evolution of phenotypes and the gene networks that control their development. For sex-specific traits, convergence offers the additional opportunity for testing whether the same gene networks follow different evolutionary trends in males versus females. Here, we use an unbiased, systematic mapping approach to compare the genetic basis of evolutionary changes in male-limited pigmentation in several pairs of Drosophila species that represent independent evolutionary transitions. We find strong evidence for repeated recruitment of the same genes to specify similar pigmentation in different species. At one of these genes, ebony, we observe convergent evolution of sexually dimorphic and monomorphic expression through cis-regulatory changes. However, this functional convergence has a different molecular basis in different species, reflecting both parallel fixation of ancestral alleles and independent origin of distinct mutations with similar functional consequences. Our results show that a strong evolutionary constraint at the gene level is compatible with a dominant role of chance at the molecular level.


Subject(s)
Biological Evolution , DNA-Binding Proteins/genetics , Drosophila Proteins/genetics , Drosophila/physiology , Gene Expression Regulation , Pigmentation/genetics , Animals , Base Sequence , Color , DNA-Binding Proteins/metabolism , Drosophila/classification , Drosophila/genetics , Drosophila/metabolism , Drosophila Proteins/metabolism , Male , Phenotype , Phylogeny , Sequence Alignment , Species Specificity
11.
Evol Dev ; 18(3): 201-9, 2016 05.
Article in English | MEDLINE | ID: mdl-27161950

ABSTRACT

Animal development is the product of distinct components and interactions-genes, regulatory networks, and cells-and it exhibits emergent properties that cannot be inferred from the components in isolation. Often the focus is on the genotype-to-phenotype map, overlooking the process of development that turns one into the other. We propose a move toward micro-evolutionary analysis of development, incorporating new tools that enable cell type resolution and single-cell microscopy. Using the sex determination pathway in Drosophila to illustrate potential avenues of research, we highlight some of the questions that these emerging technologies can address. For example, they provide an unprecedented opportunity to study heterogeneity within cell populations, and the potential to add the dimension of time to gene regulatory network analysis. Challenges still remain in developing methods to analyze this data and to increase the throughput. However this line of research has the potential to bridge the gaps between previously more disparate fields, such as population genetics and development, opening up new avenues of research.


Subject(s)
Biological Evolution , Drosophila melanogaster/genetics , Drosophila melanogaster/physiology , Gene Regulatory Networks , Animals , Brain , Gene Expression , Sex Determination Processes
12.
Genetics ; 192(4): 1465-75, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23086218

ABSTRACT

Phylogenetic analyses suggest that violations of "Dollo's law"--that is, re-evolution of lost complex structures--do occur, albeit infrequently. However, the genetic basis of such reversals has not been examined. Here, we address this question using the Drosophila sex comb, a recently evolved, male-specific morphological structure composed of modified bristles. In some species, sex comb development involves only the modification of individual bristles, while other species have more complex "rotated" sex combs that are shaped by coordinated migration of epithelial tissues. Rotated sex combs were lost in the ananassae species subgroup and subsequently re-evolved, ∼12 million years later, in Drosophila bipectinata and its sibling species. We examine the genetic basis of the differences in sex comb morphology between D. bipectinata and D. malerkotliana, a closely related species with a much simpler sex comb representing the ancestral condition. QTL mapping reveals that >50% of this difference is controlled by one chromosomal inversion that covers ∼5% of the genome. Several other, larger inversions do not contribute appreciably to the phenotype. This genetic architecture suggests that rotating sex combs may have re-evolved through changes in relatively few genes. We discuss potential developmental mechanisms that may allow lost complex structures to be regained.


Subject(s)
Biological Evolution , Drosophila/anatomy & histology , Drosophila/genetics , Animals , Chimera , Chromosome Inversion , DNA-Binding Proteins/genetics , Drosophila Proteins/genetics , Female , Genome, Insect , Male , Phenotype , Quantitative Trait Loci , Species Specificity , Transcription Factors/genetics
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