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Gene duplication and genetic exchange drive the evolution of S-RNase-based self-incompatibility in Petunia.

Type of publication Peer-reviewed
Publikationsform Original article (peer-reviewed)
Publication date 2015
Author Kubo Ken-ichi, Paape Timothy, Hatakeyama Masaomi, Entani Tetsuyuki, Takara Akie, Kajihara Kie, Tsukahara Mai, Shimizu-Inatsugi Rie, Shimizu Kentaro K, Takayama Seiji,
Project Transcriptomic analysis of polyploid species using second generation sequencers: how are they tolerant of broader range of environmental stresses?
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Original article (peer-reviewed)

Journal Nature Plants
Volume (Issue) 1(14005)
Page(s) 1 - 9
Title of proceedings Nature Plants
DOI 10.1038/nplants.2014.5

Open Access

URL http://www.nature.com/articles/nplants20145
Type of Open Access Website

Abstract

Self-incompatibility (SI) systems in flowering plants distinguish self- and non-self pollen to prevent inbreeding. While other SI systems rely on the self-recognition between specific male- and female-determinants, the Solanaceae family has a non- self recognition system resulting in the detoxification of female-determinants of S-ribonucleases (S-RNases), expressed in pistils, by multiple male-determinants of S-locus F-box proteins (SLFs), expressed in pollen. It is not known how many SLF components of this non-self recognition system there are in Solanaceae species, or how they evolved. We identified 16–20 SLFs in each S-haplotype in SI Petunia, from a total of 168 SLF sequences using large-scale next-generation sequencing and genomic polymerase chain reaction (PCR) techniques. We predicted the target S-RNases of SLFs by assuming that a particular S-allele must not have a conserved SLF that recognizes its own S-RNase, and validated these predictions by transformation experiments. A simple mathematical model confirmed that 16–20 SLF sequences would be adequate to recognize the vast majority of target S-RNases. We found evidence of gene conversion events, which we suggest are essential to the constitution of a non-self recognition system and also contribute to self-compatible mutations.
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