Author
Listed:
- Benjamin M. Moran
(Stanford University
Centro de Investigaciones Científicas de las Huastecas ‘Aguazarca’, A.C., Calnali)
- Cheyenne Y. Payne
(Stanford University
Centro de Investigaciones Científicas de las Huastecas ‘Aguazarca’, A.C., Calnali)
- Daniel L. Powell
(Stanford University
Centro de Investigaciones Científicas de las Huastecas ‘Aguazarca’, A.C., Calnali)
- Erik N. K. Iverson
(University of Texas at Austin)
- Alexandra E. Donny
(Stanford University)
- Shreya M. Banerjee
(Stanford University)
- Quinn K. Langdon
(Stanford University)
- Theresa R. Gunn
(Stanford University)
- Rebecca A. Rodriguez-Soto
(Stanford University)
- Angel Madero
(Stanford University)
- John J. Baczenas
(Stanford University)
- Korbin M. Kleczko
(Stanford University)
- Fang Liu
(Stanford University)
- Rowan Matney
(Stanford University)
- Kratika Singhal
(Stanford University)
- Ryan D. Leib
(Stanford University)
- Osvaldo Hernandez-Perez
(Centro de Investigaciones Científicas de las Huastecas ‘Aguazarca’, A.C., Calnali)
- Russell Corbett-Detig
(University of California Santa Cruz
University of California Santa Cruz)
- Judith Frydman
(Stanford University
Stanford University)
- Casey Gifford
(Stanford University
Stanford University
Stanford University)
- Manfred Schartl
(Texas State University
University of Würzburg)
- Justin C. Havird
(University of Texas at Austin)
- Molly Schumer
(Stanford University
Centro de Investigaciones Científicas de las Huastecas ‘Aguazarca’, A.C., Calnali
Howard Hughes Medical Institute)
Abstract
The evolution of reproductive barriers is the first step in the formation of new species and can help us understand the diversification of life on Earth. These reproductive barriers often take the form of hybrid incompatibilities, in which alleles derived from two different species no longer interact properly in hybrids1–3. Theory predicts that hybrid incompatibilities may be more likely to arise at rapidly evolving genes4–6 and that incompatibilities involving multiple genes should be common7,8, but there has been sparse empirical data to evaluate these predictions. Here we describe a mitonuclear incompatibility involving three genes whose protein products are in physical contact within respiratory complex I of naturally hybridizing swordtail fish species. Individuals homozygous for mismatched protein combinations do not complete embryonic development or die as juveniles, whereas those heterozygous for the incompatibility have reduced complex I function and unbalanced representation of parental alleles in the mitochondrial proteome. We find that the effects of different genetic interactions on survival are non-additive, highlighting subtle complexity in the genetic architecture of hybrid incompatibilities. Finally, we document the evolutionary history of the genes involved, showing signals of accelerated evolution and evidence that an incompatibility has been transferred between species via hybridization.
Suggested Citation
Benjamin M. Moran & Cheyenne Y. Payne & Daniel L. Powell & Erik N. K. Iverson & Alexandra E. Donny & Shreya M. Banerjee & Quinn K. Langdon & Theresa R. Gunn & Rebecca A. Rodriguez-Soto & Angel Madero , 2024.
"A lethal mitonuclear incompatibility in complex I of natural hybrids,"
Nature, Nature, vol. 626(7997), pages 119-127, February.
Handle:
RePEc:nat:nature:v:626:y:2024:i:7997:d:10.1038_s41586-023-06895-8
DOI: 10.1038/s41586-023-06895-8
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