Sporophytic Self-Incompatibility Systems: S Gene Products

Author(s):  
H.G. Dickinson ◽  
M.J.C. Crabbe ◽  
T. Gaude
Plants ◽  
2020 ◽  
Vol 9 (6) ◽  
pp. 713 ◽  
Author(s):  
Paige M. Henning ◽  
Joel S. Shore ◽  
Andrew G. McCubbin

Heterostyly employs distinct hermaphroditic floral morphs to enforce outbreeding. Morphs differ structurally in stigma/anther positioning, promoting cross-pollination, and physiologically blocking self-fertilization. Heterostyly is controlled by a self-incompatibility (S)-locus of a small number of linked S-genes specific to short-styled morph genomes. Turnera possesses three S-genes, namely TsBAHD (controlling pistil characters), TsYUC6, and TsSPH1 (controlling stamen characters). Here, we compare pistil and stamen transcriptomes of floral morphs of T. subulata to investigate hypothesized S-gene function(s) and whether hormonal differences might contribute to physiological incompatibility. We then use network analyses to identify genetic networks underpinning heterostyly. We found a depletion of brassinosteroid-regulated genes in short styled (S)-morph pistils, consistent with hypothesized brassinosteroid-inactivating activity of TsBAHD. In S-morph anthers, auxin-regulated genes were enriched, consistent with hypothesized auxin biosynthesis activity of TsYUC6. Evidence was found for auxin elevation and brassinosteroid reduction in both pistils and stamens of S- relative to long styled (L)-morph flowers, consistent with reciprocal hormonal differences contributing to physiological incompatibility. Additional hormone pathways were also affected, however, suggesting S-gene activities intersect with a signaling hub. Interestingly, distinct S-genes controlling pistil length, from three species with independently evolved heterostyly, potentially intersect with phytochrome interacting factor (PIF) network hubs which mediate red/far-red light signaling. We propose that modification of the activities of PIF hubs by the S-locus could be a common theme in the evolution of heterostyly.


2000 ◽  
Vol 12 (3) ◽  
pp. 305
Author(s):  
Vernonica E. Franklin-Tong ◽  
F. Christopher H. Franklin
Keyword(s):  

HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 462a-462
Author(s):  
Cheryl R. Hampson ◽  
Anita N. Azarenko

Self-incompatibility, a genetic mechanism enforcing out crossing, is most commonly controlled by a single, multi-allelic gene, designated the S-gene. Sporophytic self-incompatibility (SSI), a form of incompatibility determined by the parent plant rather than the gametes, is present in the Brassicaceae, Compositae and other families, and also in hazelnut (Corylus avellana L.). Little is known about the molecular basis of SSI in plants other than crucifers. An S-gene cloned from Brassica oleracea (donated by Dr. June Nasrallah, Cornell University) was used to probe genomic DNA obtained from seven hazelnut genotypes. DNA hybridization was observed in cultivars `Hall's Giant' and `Willamette'. Gene similarity was estimated to be 70-80%.


Author(s):  
Е. V. Bezlepkina ◽  
А. А. Gulyaeva ◽  
А. V. Pikunova

Self-incompatibility is one of the most important mechanisms used by flowering plants to prevent self-fertilization and, consequently, to provide the genetic diversity of population. The self-incompatibility in Prunus is controlled by two genes as minimum: S (self-incompatibility) and SFB (S haplotype-specific F-box protein).  S gene is represented in the population by a multiple allele series. Compatibility in pollination is dependent on the S allele combination of the cultivars. When S allele in the pollen is identical with one of the S alleles of the mother plant fertilization is arrested. Thus, both self-fertilization and fertilization by pollen of closely related plants (having identical S alleles) are prevented. This mechanism may be interrupted in the case of mutations in the S or SFB gene, which leads to the appearance of self-compatibility cultivars, and polyploidization, such as in sour cherry. The investigation of the S gene allele polymorphism of sweet cherry cultivars of VNIISPK breeding was performed as a part of the study of the gene collection of stone crops. Both consensus (PaConsI, PaConsII) and allele-specific (S1, S5, S9, S10) primers were used. The S-genotype of cultivars Adelina (S3/S5), Poezia (S3/S5), Siana (S3/S6), Orlovskaia feia (S3/S5) and Trosnianskaia (S5/S6) were established. The S-genotype of cultivars Malish, Podarok Orlu, Orlovskaia rozovaia and Orlovskaia yantarnaia was determined partially, as these cultivars have unique previously undescribed or very rare S alleles. Podarok Orlu variety has S9 allele and undescribed one. Malish and Orlovskaia yantarnaia varieties have S6 allele and S17 or S30 alleles supposedly, for these alleles specific primers have not yet been developed. Orlovskaya rozovaia has S6 allele and undescribed previously one.


1999 ◽  
Vol 11 (5) ◽  
pp. 971-986 ◽  
Author(s):  
Didier Cabrillac ◽  
Valérie Delorme ◽  
Jerome Garin ◽  
Véronique Ruffio-Châble ◽  
Jean-Loïc Giranton ◽  
...  

Genome ◽  
2000 ◽  
Vol 43 (5) ◽  
pp. 820-826 ◽  
Author(s):  
Andrew G McCubbin ◽  
Carmen Zuniga ◽  
Teh-hui Kao

The Solanaceae family of flowering plants possesses a type of self-incompatibility mechanism that enables the pistil to reject self pollen but accept non-self pollen for fertilization. The pistil function in this system has been shown to be controlled by a polymorphic gene at the S-locus, termed the S-RNase gene. The pollen function is believed to be controlled by another as yet unidentified polymorphic gene at the S-locus, termed the pollen S-gene. As a first step in using a functional genomic approach to identify the pollen S-gene, a genomic BAC (bacterial artificial chromosome) library of the S2S2 genotype of Petunia inflata, a self-incompatible solanaceous species, was constructed using a Ti-plasmid based BAC vector, BIBAC2. The average insert size was 136.4 kb and the entire library represented a 7.5-fold genome coverage. Screening of the library using cDNAs for the S2-RNase gene and 13 pollen-expressed genes that are linked to the S-locus yielded 51 positive clones, with at least one positive clone for each gene. Collectively, at least 2 Mb of the chromosomal region was spanned by these clones. Together, three clones that contained the S2-RNase gene spanned ~263 kb. How this BAC library and the clones identified could be used to identify the pollen S-gene and to study other aspects of self-incompatibility is discussed.Key words: bacterial artificial chromosome, Petunia inflata, pollen-pistil interactions, self-incompatibility, S-locus.


1989 ◽  
Vol 112 (2) ◽  
pp. 307-315 ◽  
Author(s):  
VERNONICA E. FRANKLIN-TONG ◽  
ERIK RUUTH ◽  
PHILIPPE MARMEY ◽  
MICHAEL J. LAWRENCE ◽  
F. CHRISTOPHER H. FRANKLIN

1994 ◽  
Vol 91 (6) ◽  
pp. 2265-2269 ◽  
Author(s):  
H. C. Foote ◽  
J. P. Ride ◽  
V. E. Franklin-Tong ◽  
E. A. Walker ◽  
M. J. Lawrence ◽  
...  

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