Genomic divergence landscape in recurrently hybridizing Chironomus sister taxa suggests stable steady state between mutual gene flow and isolation. Issue 1 (1st February 2021)
- Record Type:
- Journal Article
- Title:
- Genomic divergence landscape in recurrently hybridizing Chironomus sister taxa suggests stable steady state between mutual gene flow and isolation. Issue 1 (1st February 2021)
- Main Title:
- Genomic divergence landscape in recurrently hybridizing Chironomus sister taxa suggests stable steady state between mutual gene flow and isolation
- Authors:
- Schreiber, Dennis
Pfenninger, Markus - Abstract:
- Abstract: Divergence is mostly viewed as a progressive process often initiated by selection targeting individual loci, ultimately resulting in ever increasing genomic isolation due to linkage. However, recent studies show that this process may stall at intermediate stable equilibrium states without achieving complete genomic isolation. We tested the extent of genomic isolation between two recurrently hybridizing nonbiting midge sister taxa, Chironomus riparius and Chironomus piger, by analyzing the divergence landscape. Using a principal component-based method, we estimated that only about 28.44% of the genomes were mutually isolated, whereas the rest was still exchanged. The divergence landscape was fragmented into isolated regions of on average 30 kb, distributed throughout the genome. Selection and divergence time strongly influenced lengths of isolated regions, whereas local recombination rate only had minor impact. Comparison of divergence time distributions obtained from several coalescence-simulated divergence scenarios with the observed divergence time estimates in an approximate Bayesian computation framework favored a short and concluded divergence event in the past. Most divergence happened during a short time span about 4.5 million generations ago, followed by a stable equilibrium between mutual gene flow through ongoing hybridization for the larger part of the genome and isolation in some regions due to rapid purifying selection of introgression, supported byAbstract: Divergence is mostly viewed as a progressive process often initiated by selection targeting individual loci, ultimately resulting in ever increasing genomic isolation due to linkage. However, recent studies show that this process may stall at intermediate stable equilibrium states without achieving complete genomic isolation. We tested the extent of genomic isolation between two recurrently hybridizing nonbiting midge sister taxa, Chironomus riparius and Chironomus piger, by analyzing the divergence landscape. Using a principal component-based method, we estimated that only about 28.44% of the genomes were mutually isolated, whereas the rest was still exchanged. The divergence landscape was fragmented into isolated regions of on average 30 kb, distributed throughout the genome. Selection and divergence time strongly influenced lengths of isolated regions, whereas local recombination rate only had minor impact. Comparison of divergence time distributions obtained from several coalescence-simulated divergence scenarios with the observed divergence time estimates in an approximate Bayesian computation framework favored a short and concluded divergence event in the past. Most divergence happened during a short time span about 4.5 million generations ago, followed by a stable equilibrium between mutual gene flow through ongoing hybridization for the larger part of the genome and isolation in some regions due to rapid purifying selection of introgression, supported by high effective population sizes and recombination rates. … (more)
- Is Part Of:
- Evolution letters. Volume 5:Issue 1(2021)
- Journal:
- Evolution letters
- Issue:
- Volume 5:Issue 1(2021)
- Issue Display:
- Volume 5, Issue 1 (2021)
- Year:
- 2021
- Volume:
- 5
- Issue:
- 1
- Issue Sort Value:
- 2021-0005-0001-0000
- Page Start:
- 86
- Page End:
- 100
- Publication Date:
- 2021-02-01
- Subjects:
- Admixture inference -- islands of divergence -- reproductive isolation -- speciation
Evolution (Biology) -- Periodicals
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576.8 - Journal URLs:
- https://academic.oup.com/evlett ↗
https://onlinelibrary.wiley.com/Journal/20563744 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/evl3.204 ↗
- Languages:
- English
- ISSNs:
- 2056-3744
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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- 26925.xml