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Open AccessJournal ArticleDOI

Adaptive introgression in animals: examples and comparison to new mutation and standing variation as sources of adaptive variation.

Philip W. Hedrick
- 01 Sep 2013 - 
- Vol. 22, Iss: 18, pp 4606-4618
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TLDR
The various attributes of these three potential sources of adaptive variation are compared, including balancing selection for multiple alleles for major histocompatibility complex (MHC), S and csd genes, pesticide resistance in mice, black colour in wolves and white colour in coyotes, Neanderthal or Denisovan ancestry in humans, and mimicry genes in Heliconius butterflies are examined.
Abstract
Adaptive genetic variation has been thought to originate primarily from either new mutation or standing variation. Another potential source of adaptive variation is adaptive variants from other (donor) species that are introgressed into the (recipient) species, termed adaptive introgression. Here, the various attributes of these three potential sources of adaptive variation are compared. For example, the rate of adaptive change is generally thought to be faster from standing variation, slower from mutation and potentially intermediate from adaptive introgression. Additionally, the higher initial frequency of adaptive variation from standing variation and lower initial frequency from mutation might result in a higher probability of fixation of the adaptive variants for standing variation. Adaptive variation from introgression might have higher initial frequency than new adaptive mutations but lower than that from standing variation, again making the impact of adaptive introgression variation potentially intermediate. Adaptive introgressive variants might have multiple changes within a gene and affect multiple loci, an advantage also potentially found for adaptive standing variation but not for new adaptive mutants. The processes that might produce a common variant in two taxa, convergence, trans-species polymorphism from incomplete lineage sorting or from balancing selection and adaptive introgression, are also compared. Finally, potential examples of adaptive introgression in animals, including balancing selection for multiple alleles for major histocompatibility complex (MHC), S and csd genes, pesticide resistance in mice, black colour in wolves and white colour in coyotes, Neanderthal or Denisovan ancestry in humans, mimicry genes in Heliconius butterflies, beak traits in Darwin's finches, yellow skin in chickens and non-native ancestry in an endangered native salamander, are examined.

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Citations
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Long-term balancing selection drives evolution of immunity genes in Capsella.

TL;DR: Re reconstructing the evolution of the disease-related locus MLO2b, it is found that divergence between ancient haplotypes can be obscured by referenced based re-sequencing methods, and that trans-specific alleles can encode substantially diverged protein sequences.
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Importance of incomplete lineage sorting and introgression in the origin of shared genetic variation between two closely related pines with overlapping distributions

TL;DR: It is suggested that secondary introgression, rather than ILS, explains most of the shared nuclear genomic variation between these two species and demonstrates the complementarity of population genetics and ecological niche modeling in understanding gene flow history.
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Using Haplotype Information for Conservation Genomics.

TL;DR: An overview of how haplotype information can be used to assess historical demography, gene flow, selection, and the evolutionary outcomes of hybridization across different timescales relevant to conservation issues is provided.
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Sequential adaptive introgression of the mitochondrial genome in Drosophila yakuba and Drosophila santomea

TL;DR: At least two independent events of mtDNA introgression are uncovered in this study, including an early invasion of the D. yakuba mitochondrial genome that fully replaced the D .
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Dissecting the basis of novel trait evolution in a radiation with widespread phylogenetic discordance.

TL;DR: This analysis provides a generalizable example of how to manage discordance when identifying loci associated with trait evolution in a radiating lineage, and identifies candidate loci that could arise either from multiple lineage‐specific substitutions or standing ancestral polymorphisms.
References
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Book

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Ernst Mayr
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TL;DR: The genomic data suggest that Neandertals mixed with modern human ancestors some 120,000 years ago, leaving traces of Ne andertal DNA in contemporary humans, suggesting that gene flow from Neand Bertals into the ancestors of non-Africans occurred before the divergence of Eurasian groups from each other.
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TL;DR: It is stated that these sequences differed in the cytochromes c of various species to an extent that seemed unnecessary from the standpoint of their function.
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