Abstract

Self-incompatibility (SI) mechanisms prevent self-fertilization in flowering plants based on specific discrimination between self- and non-self pollen. Since this trait promotes outcrossing and avoids inbreeding it is a widespread mechanism of controlling sexual plant reproduction. Growers and breeders have effectively exploited SI as a tool for manipulating domesticated crops for thousands of years. However, only within the past thirty years have studies begun to elucidate the underlying molecular features of SI. The specific S-determinants and some modifier factors controlling SI have been identified in the sporophytic system exhibited by Brassica species and in the two very distinct gametophytic systems present in Papaveraceae on one side and in Solanaceae, Rosaceae, and Plantaginaceae on the other. Molecular level studies have enabled SI to SC transitions (and vice versa) to be intentionally manipulated using marker assisted breeding and targeted approaches based on transgene integration, silencing, and more recently CRISPR knock-out of SI-related factors. These scientific advances have, in turn, provided a solid basis to implement new crop production and plant breeding practices. Applications of self-(in)compatibility include widely differing objectives such as crop yield and quality improvement, marker-assisted breeding through SI genotyping, and development of hybrids for overcoming intra- and interspecific reproductive barriers. Here, we review scientific progress as well as patented applications of SI, and also highlight future prospects including further elucidation of SI systems, deepening our understanding of SI-environment relationships, and new perspectives on plant self/non-self recognition.

Highlights

  • Background on Self-IncompatibilityHumans have been aware of the link between pollination and seed production since the Neolithic period, as reflected by the laws of Hammurabi (1750 B.C.E.), these being integral parts of agriculture development (Weiss, 2015)

  • A DNA test based on the S4’-allele conferring SC in cherry, together with another test for fruit size, is routinely used in a streamlined marker-assisted seedling selection scheme by a Pacific Northwest sweet cherry breeding program (Ru et al, 2015) and it is most likely used in all sweet cherry breeding programs implementing marker assisted selection (MAS)

  • An ortholog of the A. thaliana GEX1 (Gamete Expressed) protein, that is involved in male and female gametophyte development, was significantly associated with fruit set in the cocoa CH4 genomic region

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Summary

INTRODUCTION

Humans have been aware of the link between pollination and seed production since the Neolithic period, as reflected by the laws of Hammurabi (1750 B.C.E.), these being integral parts of agriculture development (Weiss, 2015). Different Sources of SC: A Favorable Trait for Yield Enhancement In otherwise SI crops, most commercial SC cultivars derive from spontaneous and induced style- or pollen-part mutations identified and selected by growers and breeders (Figure 1A) These mutations are continually being characterized at the molecular level but use of uncharacterized sources of SC remains common. A DNA test based on the S4’-allele conferring SC in cherry, together with another test for fruit size, is routinely used in a streamlined marker-assisted seedling selection scheme by a Pacific Northwest sweet cherry breeding program (Ru et al, 2015) and it is most likely used in all sweet cherry breeding programs implementing MAS In another example, gene-specific S-locus markers have been developed at the Saskatoon Research and Development Center in Canada to select SC genotypes in yellow mustard (Sinapis alba L.) (Zeng and Cheng, 2014). 4/2 (S-IandS-IISLGa,b)/ (S-IISP11a,b) 18 (S1-S18) 7/7 (S1-10/S1-10))a 9/10 (Rs-SRK1–21/SP111-21)a 15 (RsS1-40))a

Method
Method for breeding
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CONCLUDING REMARKS
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