Repeated Evolution of Asexuality Involves Convergent Gene Expression Changes

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Repeated Evolution of Asexuality Involves Convergent Gene Expression Changes. / Parker, Darren J; Bast, Jens; Jalvingh, Kirsten et al.
Yn: Molecular Biology and Evolution, Cyfrol 36, Rhif 2, 01.02.2019, t. 350-364.

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HarvardHarvard

Parker, DJ, Bast, J, Jalvingh, K, Dumas, Z, Robinson-Rechavi, M & Schwander, T 2019, 'Repeated Evolution of Asexuality Involves Convergent Gene Expression Changes', Molecular Biology and Evolution, cyfrol. 36, rhif 2, tt. 350-364. https://doi.org/10.1093/molbev/msy217

APA

Parker, D. J., Bast, J., Jalvingh, K., Dumas, Z., Robinson-Rechavi, M., & Schwander, T. (2019). Repeated Evolution of Asexuality Involves Convergent Gene Expression Changes. Molecular Biology and Evolution, 36(2), 350-364. https://doi.org/10.1093/molbev/msy217

CBE

Parker DJ, Bast J, Jalvingh K, Dumas Z, Robinson-Rechavi M, Schwander T. 2019. Repeated Evolution of Asexuality Involves Convergent Gene Expression Changes. Molecular Biology and Evolution. 36(2):350-364. https://doi.org/10.1093/molbev/msy217

MLA

VancouverVancouver

Parker DJ, Bast J, Jalvingh K, Dumas Z, Robinson-Rechavi M, Schwander T. Repeated Evolution of Asexuality Involves Convergent Gene Expression Changes. Molecular Biology and Evolution. 2019 Chw 1;36(2):350-364. Epub 2018 Tach 16. doi: 10.1093/molbev/msy217

Author

Parker, Darren J ; Bast, Jens ; Jalvingh, Kirsten et al. / Repeated Evolution of Asexuality Involves Convergent Gene Expression Changes. Yn: Molecular Biology and Evolution. 2019 ; Cyfrol 36, Rhif 2. tt. 350-364.

RIS

TY - JOUR

T1 - Repeated Evolution of Asexuality Involves Convergent Gene Expression Changes

AU - Parker, Darren J

AU - Bast, Jens

AU - Jalvingh, Kirsten

AU - Dumas, Zoé

AU - Robinson-Rechavi, Marc

AU - Schwander, Tanja

PY - 2019/2/1

Y1 - 2019/2/1

N2 - Asexual reproduction has evolved repeatedly from sexual ancestors across a wide range of taxa. Whereas the costs and benefits associated with asexuality have received considerable attention, the molecular changes underpinning the evolution of asexual reproduction remain relatively unexplored. In particular, it is completely unknown whether the repeated evolution of asexual phenotypes involves similar molecular changes, as previous studies have focused on changes occurring in single lineages. Here, we investigate the extent of convergent gene expression changes across five independent transitions to asexuality in stick insects. We compared gene expression of asexual females to females of close sexual relatives in whole-bodies, reproductive tracts, and legs. We identified a striking amount of convergent gene expression change (up to 8% of genes), greatly exceeding that expected by chance. Convergent changes were also tissue-specific, and most likely driven by selection for functional changes. Genes showing convergent changes in the reproductive tract were associated with meiotic spindle formation and centrosome organization. These genes are particularly interesting as they can influence the production of unreduced eggs, a key barrier to asexual reproduction. Changes in legs and whole-bodies were likely involved in female sexual trait decay, with enrichment in terms such as sperm-storage and pigmentation. By identifying changes occurring across multiple independent transitions to asexuality, our results provide a rare insight into the molecular basis of asexual phenotypes and suggest that the evolutionary path to asexuality is highly constrained, requiring repeated changes to the same key genes.

AB - Asexual reproduction has evolved repeatedly from sexual ancestors across a wide range of taxa. Whereas the costs and benefits associated with asexuality have received considerable attention, the molecular changes underpinning the evolution of asexual reproduction remain relatively unexplored. In particular, it is completely unknown whether the repeated evolution of asexual phenotypes involves similar molecular changes, as previous studies have focused on changes occurring in single lineages. Here, we investigate the extent of convergent gene expression changes across five independent transitions to asexuality in stick insects. We compared gene expression of asexual females to females of close sexual relatives in whole-bodies, reproductive tracts, and legs. We identified a striking amount of convergent gene expression change (up to 8% of genes), greatly exceeding that expected by chance. Convergent changes were also tissue-specific, and most likely driven by selection for functional changes. Genes showing convergent changes in the reproductive tract were associated with meiotic spindle formation and centrosome organization. These genes are particularly interesting as they can influence the production of unreduced eggs, a key barrier to asexual reproduction. Changes in legs and whole-bodies were likely involved in female sexual trait decay, with enrichment in terms such as sperm-storage and pigmentation. By identifying changes occurring across multiple independent transitions to asexuality, our results provide a rare insight into the molecular basis of asexual phenotypes and suggest that the evolutionary path to asexuality is highly constrained, requiring repeated changes to the same key genes.

KW - Animals

KW - Biological Evolution

KW - Female

KW - Gene Expression

KW - Insecta/genetics

KW - Reproduction, Asexual/genetics

U2 - 10.1093/molbev/msy217

DO - 10.1093/molbev/msy217

M3 - Article

C2 - 30445505

VL - 36

SP - 350

EP - 364

JO - Molecular Biology and Evolution

JF - Molecular Biology and Evolution

SN - 0737-4038

IS - 2

ER -