ArticlePlant cell reports2010
Self-compatibility in 'Cristobalina' sweet cherry is not associated with duplications or modified transcription levels of S-locus genes.
Article in Plant cell reports, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 22 citations in OpenAlex.
- Identification of Self-Incompatibility Related Genes in Sweet Cherry Based on Transcriptomic Analysis.Biology · 2025Article
- Evaluation of the S-locus in Prunus domestica, characterization, phylogeny and 3D modelling.PloS one · 2021Article
- Ubiquitination of SPlant physiology · 2020Article
- Overcoming self-incompatibility in grasses: a pathway to hybrid breeding.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2016Review
- Methylation of the S f locus in almond is associated with S-RNase loss of function.Plant molecular biology · 2014Article
- Self-compatibility in 'Zaohong' Japanese apricot is associated with the loss of function of pollen S genes.Molecular biology reports · 2013Article
- Article
- Physical mapping of a pollen modifier locus controlling self-incompatibility in apricot and synteny analysis within the Rosaceae.Plant molecular biology · 2012Article
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Authors and funding
3 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Sweet cherry shows S-RNase-based gametophytic self-incompatibility, which prevents self- and cross-fertilization between genetically related individuals. The specificity of the self-incompatible reaction is determined by two genes located in the S-locus. These encode a pistil-expressed ribonuclease (S-RNase) that inhibits self pollen tube growth, and a pollen-expressed F-box protein (SFB) that may be involved in the cytotoxicity of self-S-RNases. Initial genetic and pollination studies in a self-compatible sweet cherry cultivar, 'Cristobalina' (S (3) S (6)), showed that self-compatibility was caused by the loss of pollen function of both haplotypes (S (3) and S (6)). In this study, we further characterize self-compatibility in this genotype by molecular analysis of the S-locus. DNA blot analyses using S-RNase and SFB probes show no duplications of 'Cristobalina' S-locus genes or differences in the restriction patterns when compared with self-incompatible cultivars with the same S-genotype. Furthermore, reverse transcriptase-PCR of S-locus genes and quantitative reverse transcription-PCR of SFBs revealed no differences at the transcription level when compared with a self-incompatible genotype. The results of this study show that no differences at the S-locus can be correlated with self-compatibility, indicating the possible involvement of non-S-locus modifiers in self-incompatibility breakdown in this cultivar.
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