The Genomic Selfing Syndrome Accompanies the Evolutionary Breakdown of Heterostyly

Author:

Wang Xin-Jia123ORCID,Barrett Spencer C H4,Zhong Li13,Wu Zhi-Kun5,Li De-Zhu12,Wang Hong1,Zhou Wei12

Affiliation:

1. CAS Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan, China

2. Plant Germplasm and Genomics Center, Germplasm Bank of Wild Species, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan, China

3. University of Chinese Academy of Sciences, Beijing, China

4. Department of Ecology and Evolutionary Biology, University of Toronto, Toronto, Canada

5. Department of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang, Guizhou, China

Abstract

AbstractThe evolutionary transition from outcrossing to selfing can have important genomic consequences. Decreased effective population size and the reduced efficacy of selection are predicted to play an important role in the molecular evolution of the genomes of selfing species. We investigated evidence for molecular signatures of the genomic selfing syndrome using 66 species of Primula including distylous (outcrossing) and derived homostylous (selfing) taxa. We complemented our comparative analysis with a microevolutionary study of P. chungensis, which is polymorphic for mating system and consists of both distylous and homostylous populations. We generated chloroplast and nuclear genomic data sets for distylous, homostylous, and distylous–homostylous species and identified patterns of nonsynonymous to synonymous divergence (dN/dS) and polymorphism (πN/πS) in species or lineages with contrasting mating systems. Our analysis of coding sequence divergence and polymorphism detected strongly reduced genetic diversity and heterozygosity, decreased efficacy of purifying selection, purging of large-effect deleterious mutations, and lower rates of adaptive evolution in samples from homostylous compared with distylous populations, consistent with theoretical expectations of the genomic selfing syndrome. Our results demonstrate that self-fertilization is a major driver of molecular evolutionary processes with genomic signatures of selfing evident in both old and relatively young homostylous populations.

Funder

Strategic Priority Research Program of the Chinese Academy of Sciences

National Natural Science Foundation of China

Yunling Scholarship of Yunnan Province

Light of West China Program of the Chinese Academy of Sciences

Discovery Grant from the Natural Sciences and Engineering Research Council of Canada

Publisher

Oxford University Press (OUP)

Subject

Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference106 articles.

1. Weak selection and protein evolution;Akashi;Genetics,2012

2. The evolution of selfing is accompanied by reduced efficacy of selection and purging of deleterious mutations;Arunkumar;Genetics,2015

3. Selection, recombination and demographic history in Drosophila miranda;Bachtrog;Genetics,2006

4. Self-compatibility and establishment after ‘long-distance’ dispersal;Baker;Evolution,1955

5. Evolution and Function of Heterostyly

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