The genomics of mimicry: Gene expression throughout development provides insights into convergent and divergent phenotypes in a Müllerian mimicry system

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The genomics of mimicry : Gene expression throughout development provides insights into convergent and divergent phenotypes in a Müllerian mimicry system. / Stuckert, Adam M. M.; Chouteau, Mathieu; McClure, Melanie; LaPolice, Troy M.; Linderoth, Tyler; Nielsen, Rasmus; Summers, Kyle; MacManes, Matthew D.

In: Molecular Ecology, Vol. 30, No. 16, 2021, p. 4039-4061.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Stuckert, AMM, Chouteau, M, McClure, M, LaPolice, TM, Linderoth, T, Nielsen, R, Summers, K & MacManes, MD 2021, 'The genomics of mimicry: Gene expression throughout development provides insights into convergent and divergent phenotypes in a Müllerian mimicry system', Molecular Ecology, vol. 30, no. 16, pp. 4039-4061. https://doi.org/10.1111/mec.16024

APA

Stuckert, A. M. M., Chouteau, M., McClure, M., LaPolice, T. M., Linderoth, T., Nielsen, R., Summers, K., & MacManes, M. D. (2021). The genomics of mimicry: Gene expression throughout development provides insights into convergent and divergent phenotypes in a Müllerian mimicry system. Molecular Ecology, 30(16), 4039-4061. https://doi.org/10.1111/mec.16024

Vancouver

Stuckert AMM, Chouteau M, McClure M, LaPolice TM, Linderoth T, Nielsen R et al. The genomics of mimicry: Gene expression throughout development provides insights into convergent and divergent phenotypes in a Müllerian mimicry system. Molecular Ecology. 2021;30(16):4039-4061. https://doi.org/10.1111/mec.16024

Author

Stuckert, Adam M. M. ; Chouteau, Mathieu ; McClure, Melanie ; LaPolice, Troy M. ; Linderoth, Tyler ; Nielsen, Rasmus ; Summers, Kyle ; MacManes, Matthew D. / The genomics of mimicry : Gene expression throughout development provides insights into convergent and divergent phenotypes in a Müllerian mimicry system. In: Molecular Ecology. 2021 ; Vol. 30, No. 16. pp. 4039-4061.

Bibtex

@article{475c64f93acd446ca69b9f2ddee4666b,
title = "The genomics of mimicry: Gene expression throughout development provides insights into convergent and divergent phenotypes in a M{\"u}llerian mimicry system",
abstract = "A common goal in evolutionary biology is to discern the mechanisms that produce the astounding diversity of morphologies seen across the tree of life. Aposematic species, those with a conspicuous phenotype coupled with some form of defence, are excellent models to understand the link between vivid colour pattern variations, the natural selection shaping it, and the underlying genetic mechanisms underpinning this variation. Mimicry systems in which multiple species share the same conspicuous phenotype can provide an even better model for understanding the mechanisms of colour production in aposematic species, especially if comimics have divergent evolutionary histories. Here we investigate the genetic mechanisms by which vivid colour and pattern are produced in a M{\"u}llerian mimicry complex of poison frogs. We did this by first assembling a high-quality de novo genome assembly for the mimic poison frog Ranitomeya imitator. This assembled genome is 6.8 Gbp in size, with a contig N50 of 300 Kbp R. imitator and two colour morphs from both Ranitomeya fantastica and R. variabilis which R. imitator mimics. We identified a large number of pigmentation and patterning genes that are differentially expressed throughout development, many of them related to melanocyte development, melanin synthesis, iridophore development and guanine synthesis. Polytypic differences within species may be the result of differences in expression and/or timing of expression, whereas convergence for colour pattern between species does not appear to be due to the same changes in gene expression. In addition, we identify the pteridine synthesis pathway (including genes such as qdpr and xdh) as a key driver of the variation in colour between morphs of these species. Finally, we hypothesize that genes in the keratin family are important for producing different structural colours within these frogs.",
keywords = "amphibians, aposematism, colour pattern, colour production, Dendrobatidae, Ranitomeya",
author = "Stuckert, {Adam M. M.} and Mathieu Chouteau and Melanie McClure and LaPolice, {Troy M.} and Tyler Linderoth and Rasmus Nielsen and Kyle Summers and MacManes, {Matthew D.}",
note = "Publisher Copyright: {\textcopyright} 2021 The Authors. Molecular Ecology published by John Wiley & Sons Ltd.",
year = "2021",
doi = "10.1111/mec.16024",
language = "English",
volume = "30",
pages = "4039--4061",
journal = "Molecular Ecology",
issn = "0962-1083",
publisher = "Wiley-Blackwell",
number = "16",

}

RIS

TY - JOUR

T1 - The genomics of mimicry

T2 - Gene expression throughout development provides insights into convergent and divergent phenotypes in a Müllerian mimicry system

AU - Stuckert, Adam M. M.

AU - Chouteau, Mathieu

AU - McClure, Melanie

AU - LaPolice, Troy M.

AU - Linderoth, Tyler

AU - Nielsen, Rasmus

AU - Summers, Kyle

AU - MacManes, Matthew D.

N1 - Publisher Copyright: © 2021 The Authors. Molecular Ecology published by John Wiley & Sons Ltd.

PY - 2021

Y1 - 2021

N2 - A common goal in evolutionary biology is to discern the mechanisms that produce the astounding diversity of morphologies seen across the tree of life. Aposematic species, those with a conspicuous phenotype coupled with some form of defence, are excellent models to understand the link between vivid colour pattern variations, the natural selection shaping it, and the underlying genetic mechanisms underpinning this variation. Mimicry systems in which multiple species share the same conspicuous phenotype can provide an even better model for understanding the mechanisms of colour production in aposematic species, especially if comimics have divergent evolutionary histories. Here we investigate the genetic mechanisms by which vivid colour and pattern are produced in a Müllerian mimicry complex of poison frogs. We did this by first assembling a high-quality de novo genome assembly for the mimic poison frog Ranitomeya imitator. This assembled genome is 6.8 Gbp in size, with a contig N50 of 300 Kbp R. imitator and two colour morphs from both Ranitomeya fantastica and R. variabilis which R. imitator mimics. We identified a large number of pigmentation and patterning genes that are differentially expressed throughout development, many of them related to melanocyte development, melanin synthesis, iridophore development and guanine synthesis. Polytypic differences within species may be the result of differences in expression and/or timing of expression, whereas convergence for colour pattern between species does not appear to be due to the same changes in gene expression. In addition, we identify the pteridine synthesis pathway (including genes such as qdpr and xdh) as a key driver of the variation in colour between morphs of these species. Finally, we hypothesize that genes in the keratin family are important for producing different structural colours within these frogs.

AB - A common goal in evolutionary biology is to discern the mechanisms that produce the astounding diversity of morphologies seen across the tree of life. Aposematic species, those with a conspicuous phenotype coupled with some form of defence, are excellent models to understand the link between vivid colour pattern variations, the natural selection shaping it, and the underlying genetic mechanisms underpinning this variation. Mimicry systems in which multiple species share the same conspicuous phenotype can provide an even better model for understanding the mechanisms of colour production in aposematic species, especially if comimics have divergent evolutionary histories. Here we investigate the genetic mechanisms by which vivid colour and pattern are produced in a Müllerian mimicry complex of poison frogs. We did this by first assembling a high-quality de novo genome assembly for the mimic poison frog Ranitomeya imitator. This assembled genome is 6.8 Gbp in size, with a contig N50 of 300 Kbp R. imitator and two colour morphs from both Ranitomeya fantastica and R. variabilis which R. imitator mimics. We identified a large number of pigmentation and patterning genes that are differentially expressed throughout development, many of them related to melanocyte development, melanin synthesis, iridophore development and guanine synthesis. Polytypic differences within species may be the result of differences in expression and/or timing of expression, whereas convergence for colour pattern between species does not appear to be due to the same changes in gene expression. In addition, we identify the pteridine synthesis pathway (including genes such as qdpr and xdh) as a key driver of the variation in colour between morphs of these species. Finally, we hypothesize that genes in the keratin family are important for producing different structural colours within these frogs.

KW - amphibians

KW - aposematism

KW - colour pattern

KW - colour production

KW - Dendrobatidae

KW - Ranitomeya

U2 - 10.1111/mec.16024

DO - 10.1111/mec.16024

M3 - Journal article

C2 - 34145931

AN - SCOPUS:85110150475

VL - 30

SP - 4039

EP - 4061

JO - Molecular Ecology

JF - Molecular Ecology

SN - 0962-1083

IS - 16

ER -

ID: 336745948