4.8 Article

Butterfly genome reveals promiscuous exchange of mimicry adaptations among species

Journal

NATURE
Volume 487, Issue 7405, Pages 94-98

Publisher

NATURE PORTFOLIO
DOI: 10.1038/nature11041

Keywords

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Funding

  1. Leverhulme Trust
  2. John Fell Fund
  3. Christ Church College, Oxford
  4. Royal Society
  5. NSF
  6. NIH
  7. CNRS
  8. ERC
  9. Banco de la Republica
  10. COLCIENCAS
  11. BBSRC
  12. BBSRC [BB/H014357/1, BB/H014268/1, BB/G00661X/1, BB/E006191/1, BB/H01439X/1, BB/G006903/1, BB/G530425/1] Funding Source: UKRI
  13. MRC [G0900740] Funding Source: UKRI
  14. Biotechnology and Biological Sciences Research Council [BB/G00661X/1, BB/H014268/1, BB/H01439X/1, BB/E006191/1, BB/G530425/1, BB/G006903/1, BB/H014357/1] Funding Source: researchfish
  15. Medical Research Council [G0900740] Funding Source: researchfish
  16. Direct For Biological Sciences
  17. Division Of Environmental Biology [1020136, 1020355, 844244, 1316037] Funding Source: National Science Foundation
  18. Direct For Biological Sciences
  19. Division Of Integrative Organismal Systems [1305686] Funding Source: National Science Foundation
  20. Direct For Biological Sciences
  21. Div Of Biological Infrastructure [0959864, 0905698] Funding Source: National Science Foundation

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The evolutionary importance of hybridization and introgression has long been debated(1). Hybrids are usually rare and unfit, but even infrequent hybridization can aid adaptation by transferring beneficial traits between species. Here we use genomic tools to investigate introgression in Heliconius, a rapidly radiating genus of neotropical butterflies widely used in studies of ecology, behaviour, mimicry and speciation(2-5). We sequenced the genome of Heliconius melpomene and compared it with other taxa to investigate chromosomal evolution in Lepidoptera and gene flow among multiple Heliconius species and races. Among 12,669 predicted genes, biologically important expansions of families of chemosensory and Hox genes are particularly noteworthy. Chromosomal organization has remained broadly conserved since the Cretaceous period, when butterflies split from the Bombyx (silkmoth) lineage. Using genomic resequencing, we show hybrid exchange of genes between three co-mimics, Heliconius melpomene, Heliconius timareta and Heliconius elevatus, especially at two genomic regions that control mimicry pattern. We infer that closely related Heliconius species exchange protective colour-pattern genes promiscuously, implying that hybridization has an important role in adaptive radiation.

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