M
Mathieu Joron
Researcher at University of Montpellier
Publications - 89
Citations - 7289
Mathieu Joron is an academic researcher from University of Montpellier. The author has contributed to research in topics: Heliconius & Müllerian mimicry. The author has an hindex of 37, co-authored 83 publications receiving 6224 citations. Previous affiliations of Mathieu Joron include Smithsonian Institution & University College London.
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Journal ArticleDOI
Inversion breakpoints and the evolution of supergenes.
Romain Villoutreix,Diego Ayala,Mathieu Joron,Zachariah Gompert,Jeffrey L. Feder,Patrik Nosil +5 more
Abstract: The coexistence of discrete morphs that differ in multiple traits is common within natural populations of many taxa. Such morphs are often associated with chromosomal inversions, presumably because the recombination suppressing effects of inversions help maintain alternate adaptive combinations of alleles across the multiple loci affecting these traits. However, inversions can also harbour selected mutations at their breakpoints, leading to their rise in frequency in addition to (or independent from) their role in recombination suppression. In this review, we first describe the different ways that breakpoints can create mutations. We then critically examine the evidence for the breakpoint-mutation and recombination suppression hypotheses for explaining the existence of discrete morphs associated with chromosomal inversions. We find that the evidence that inversions are favoured due to recombination suppression is often indirect. The evidence that breakpoints harbour mutations that are adaptive is also largely indirect, with the characterization of inversion breakpoints at the sequence level being incomplete in most systems. Direct tests of the role of suppressed recombination and breakpoint mutations in inversion evolution are thus needed. Finally, we emphasize how the two hypotheses of recombination suppression and breakpoint mutation can act in conjunction, with implications for understanding the emergence of supergenes and their evolutionary dynamics. We conclude by discussing how breakpoint characterization could improve our understanding of complex, discrete phenotypic forms in nature.
Posted ContentDOI
Major improvements to the Heliconius melpomene genome assembly used to confirm 10 chromosome fusion events in 6 million years of butterfly evolution
John W. Davey,Mathieu Chouteau,Sarah L. Barker,Luana S. Maroja,Simon W. Baxter,Fraser Simpson,Mathieu Joron,James Mallet,Kanchon K. Dasmahapatra,Chris D. Jiggins +9 more
TL;DR: A substantially improved assembly of the Heliconius melpomene genome is presented, developed using novel methods that should be applicable to improving other genome assemblies produced using short read sequencing.
Journal ArticleDOI
Similar predator aversion for natural prey with diverse toxicity levels
TL;DR: Protection against predators induced by chemical defences of 13 lepidopteran species belonging to six mimicry complexes is compared, finding that prey with a two- to three-fold difference in toxin content generated similar avoidance learning indices.
EVOLUTION OF DIVERSITY IN WARNING COLOR AND MIMICRY: Polymorphisms, Shifting
James Mallet,Mathieu Joron +1 more
TL;DR: Mullerian and Batesian color patterns are often determined by relatively few pattern-regulating loci with major effects as discussed by the authors, which can be explained by the shape of a "number-dependent" selection function first modeled by Fritz Muller in 1879.
Posted ContentDOI
Mutation accumulation in chromosomal inversions maintains wing pattern polymorphism in a butterfly
Paul Jay,Mathieu Chouteau,Annabel Whibley,Héloïse Bastide,Violaine Llaurens,Hugues Parrinello,Mathieu Joron +6 more
TL;DR: The factors maintaining multiple mimetic morphs in the butterfly Heliconius numata are studied to suggest that many complex polymorphisms, instead of representing adaptations to the existence of alternative ecological optima, could be maintained primarily because chromosomal rearrangements are prone to carrying recessive harmful mutations.