Why Self-fertilizing Plants Still Exist in Wild Populations: Diversity Assurance through Stress-Induced Male Sterility May Promote Selective Outcrossing and Recombination
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Date
2020-03-03
Date Issued
ISI Journal
Impact factor: 2.603 (Year: 2020)
Authors
Citation
Maarten van Ginkel, Ronald Flipphi. (3/3/2020). Why Self-fertilizing Plants Still Exist in Wild Populations: Diversity Assurance through Stress-Induced Male Sterility May Promote Selective Outcrossing and Recombination. Agronomy, 10 (3).
Abstract
Climate change creates challenges for wild species, but plants have survived and adapted
to similar changes in their evolutionary past. Most plants were originally outcrossing, one theoretical
genetic reason being that self-fertilization does not create novel recombinants that allow adaptation.
Thus selfing seems an evolutionary “dead end”. Nevertheless, self-fertilizing plants make up 14%
of seed plant species. We offer a new interpretation of a response by self-fertilizing wild species to
extreme existential threats, which creates novel recombinant progeny. This proposed mechanism
goes beyond reproductive assurance, the usual explanation of selfing. Extreme stress, such as
excessive heat within a specific window, first makes plants male-sterile, while female organs remain
functional and can receive wind-borne pollen from any of the few nearby stress-tolerant individuals.
Thus stress-induced male sterility enables and/or enhances outcrossing in selfing plants. Although in
practice this proposed mechanism requires very special circumstances and operates only in certain
species with conducive floral traits, we posit that over evolutionary time even such rare events
can make a significant lasting impact on a species’ survival in changing conditions. This proposed
mechanism, which we call Diversity Assurance, allows a population subject to severe stress to
sample preferentially those genes that underpin tolerance to that specific stress. These genes are
then recombined in subsequent generations, along with the male-sterility-under-stress trait of the
female parent. This contributes in part to explain the effective evolution and hence persistence of
self-fertilizing species. Diversity Assurance, we propose, is an adaptive mechanism that has been
selected under extreme stress, underpinned by a simple loss-of-function of the male reproductive
system. It may be triggered not only by heat, but also by other stressors. This proposed mechanism
helps to explain why even highly self-fertilizing plant species remain able to respond to environmental
changes through triggered outcrossing.
