Xiaoping Lian
Shilai Zhang
Guangfu Huang
Liyu Huang
Jing Zhang
Fengyi Hu- State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, Research Center for Perennial Rice Engineering and Technology of Yunnan, School of Agriculture, Yunnan University, Kunming, China
Oryza longistaminata, a wild species of African origin, has been reported to exhibit self-incompatibility (SI). However, the genetic pattern of its SI remained unknown. In this study, we conducted self-pollination and reciprocal cross-pollination experiments to verify that O. longistaminata is a strictly self-incompatible species. The staining of pollen with aniline blue following self-pollination revealed that although pollen could germinate on the stigma, the pollen tube was unable to enter the style to complete pollination, thereby resulting in gametophytic self-incompatibility (GSI). LpSDUF247, a S-locus male determinant in the gametophytic SI system of perennial ryegrass, is predicted to encode a DUF247 protein. On the basic of chromosome alignment with LpSDUF247, we identified OlSS1 and OlSS2 as Self-Incompatibility Stamen candidate genes in O. longistaminata. Chromosome segment analysis revealed that the Self-Incompatibility Pistil candidate gene of O. longistaminata (OlSP) is a polymorphic gene located in a region flanking OlSS1. OlSS1 was expressed mainly in the stamens, whereas OlSS2 was expressed in both the stamens and pistils. OlSP was specifically highly expressed in the pistils, as revealed by RT-PCR and qRT-PCR analyses. Collectively, our observations indicate the occurrence of GSI in O. longistaminata and that this process is potentially controlled by OlSS1, OlSS2, and OlSP. These findings provide further insights into the genetic mechanisms underlying self-compatibility in plants.
Introduction
Self-incompatibility (SI) is a reproductive mechanism of higher plants for preventing inbreeding by inhibiting self-pollination, and has been widely observed in Brassicaceae, Solanaceae, Rosaceae, Plantaginaceae, Scrophulariaceae, Gramineae, and Rutaceae (Pandey, 1960; Goring et al., 1993; Vaughan, 1994; Dickinson, 1995; McCormick, 1998; Liu et al., 2014; Iwano et al., 2015; Li et al., 2017; Ye et al., 2018; Liang et al., 2020). SI is described as a mechanism whereby plants are able to produce functional male and female gametes, but are incapable of producing seeds subsequent to self-pollination or the cross-pollination of plants containing SI alleles (Pandey, 1960; Takayama and Isogai, 2005). SI was divided into gametophytic self-incompatibility (GSI) and sporophytic self-incompatibility (SSI), which is defined based on the genetic mode of control of the incompatibility phenotype in pollen (de Nettancourt, 1997; McCubbin and Kao, 2000; Silva and Goring, 2001). In GSI, incompatibility is determined by pollen genotype, where growth inhibition of incompatible pollen occurs mainly in the style. In SSI, pollen grain incompatibility is determined by the diploid genome of the parent, in which mature pollen carry SI signal elements secreted by the tapetum, which lead to inhibiting of the germination of incompatible pollen on the stigma surface (de Nettancourt, 1997; Hiscock and Tabah, 2003; Hiscock and McInnis, 2004). The genetic mechanism of SI is dependent on signal transmission controlled by a single or multiple genetic loci between pollen and stigma (Franklin-Tong et al., 1988; Franklin-Tong and Franklin, 2003; Castric and Vekemans, 2004). The genetic loci associated with SI characteristically show high polymorphism, with respect to both the number of S alleles and differences in nucleotide sequences (Vekemans and Slatkin, 1994).
The SI system in Gramineae is GSI, which is thought to be controlled by two non-linked and polymorphic multi-allelic S and Z loci (Lundqvist, 1954; Cornish et al., 1979; Baumann et al., 2000; Thorogood et al., 2002). The S and Z loci in Lolium perenne L. have been found to be correspond to syntenic regions of chromosomes 5 and 4 in the genome of O. sativa, respectively (Yang et al., 2009). In total, 10 SI candidate genes have been identified in the SI cDNA libraries of L. perenne, and qRT-PCR analysis has revealed a rapid increase in the expression of these genes following pollen–stigma contact (Yang et al., 2009). Subsequently, nine candidate genes associated with SI were screened from L. perenne using molecular markers, and on the basis of expression profiling and nucleotide diversity assessment, two Z-linked genes, a ubiquitin-specific protease and a LpDUF247 gene, have been identified as the most plausible candidates for the S-Z SI system (Shinozuka et al., 2010). In further studies, a total of 10,177 individuals of L. perenne from seven different mapping populations segregating for S locus showed a highly polymorphic gene encoding for a protein containing a DUF247 was fully predictive of known S-locus genotypes at the amino acid level (Manzanares et al., 2016). In addition, genome wide association studies and BLAST alignment with the Brachypodium physical map revealed highly significantly associated markers with peak associations from the chromosomal locations of candidate SI genes S- and Z-DUF247 (Thorogood et al., 2017). LpSDUF247 is considered to be a S-locus male determinant in the gametophytic SI system that has five haplotypes with sequence polymorphism, which is a typical characteristic of SI. However, the molecular mechanisms underlying the regulation of SI in L. perenne have yet to be clarified (Thorogood et al., 2002; Shinozuka et al., 2010; Manzanares et al., 2016).
Oryza longistaminata is an AA-genome wild Oryza species of African origin that exhibits SI (Nayar, 1967). O. longistaminata has numerous desirable traits, such as long stigma and large anthers (Morishima, 1967), a rhizome (Ghesquiere, 2008), and high resistance to abiotic and biotic stresses (Khush et al., 1990; Song et al., 1995; Hu et al., 2003; Dong et al., 2017), and accordingly could represent a beneficial resource from the perspective of rice breeding. However, SI limits its free mating and hinders the exploitation of such desirable traits in rice cultivar improvement. In the present study, we identified a polymorphic S-locus associated with SI in this species, which will provide a basis for the determination of genetic patterns and molecular mechanisms of SI. Accordingly, we believe that the findings of this study could potentially facilitate exploitation of the desirable traits of O. longistaminata.
Materials and Methods
Plant Materials
For the determining the SI of O. longistaminata, we used the germplasms OlMK23 and OlMK68, which were originally collected from Ethiopia and were kindly provided by Dr. Melaku Getachew of the Institute of Biotechnology, College of Natural and Computational Sciences, Addis Ababa University, Ethiopia. For reciprocal hybrid testing, OlMK68 and OlMK23 plants were cultivated at Jinghong, Yunnan Province, China (21°59′N, 87 100°44′E, 611 m a.s.l.). For hybridization experiments, stamens were removed manually from the pollen recipients and mature pollen was collected from the pollen donors.
Reciprocal Hybrids and Statistics
The O. longistaminata germplasms OlMK23 and OlMK68, and their reciprocal hybrids, each of which was represented by 10 samples, were cultivated for SI testing. For the reciprocal hybrids, the stamens were removed from a pollen recipient and mature pollen grains were collected from a pollen donor, after which plant were cross-pollinated and bagged. The seed-setting rate of OlMK23, OlMK68, and their reciprocal hybrids was determined after harvesting. Statistical analyses of seed-setting rate were based on the ratio between the number of harvested mature seeds and the total number of pollinated flowers in 10 independent pollination experiments.
Aniline Blue Staining
At 5 min, 30 min, 1 h, and 2 h following self-/cross-pollination, more than 10 pollinated O. longistaminata and O. sativa pistils were collected and subsequently fixed overnight in Carnoy’s solution (90 mL of 50% ethanol, 5 mL of formaldehyde, and 5 mL of acetic acid). The pistils were then sequentially rehydrated with ethanol (50, 30, and 10%, each for 10 min) and then washed with deionized water. Thereafter, the pistils were softened in 1 M NaOH for 45 min at 55°C and stained with water-soluble aniline blue [0.1% (W/V) aniline blue and 0.1 M K2HPO4, pH 8.5] for 6 h in the dark at room temperature. The stained pistils were visualized by fluorescence microscopy.
Identified and Syntenic Analysis of OlSSs and OlSP
LpSDUF247 is a male component of the S-locus in L. perenne and is syntenic with O. sativa (Manzanares et al., 2016). OsDUF247 (Os05g0197900), which corresponds to LpSDUF247, is located in the 6,030–6,090 kb region of O. sativa chromosome A05. Comparative genomics analyses were performed by comparing the genome sequences of O. longistaminata with chromosome 5 of O. sativa. OlSS1 on Contig10 of O. longistaminata corresponds to OsDUF247 (Os05g0197900). Sequence analysis was performed on the sequence flanking OlSS1 to identify candidate polymorphic sequences. Haplotype and sequence polymorphism analyses of OlSS1, OlSS2, and OlSP were based on published transcriptome sequencing data (Zhang et al., 2015), whereas analysis of the conserved domain of OlSS1, OlSS2, and OlSP was performed using SMART1.
RNA Isolation
The roots, stems, leaves, stamens, and pistils of O. longistaminata were used for tissue-specific expression analysis. The stamens were collected to determine the expression of OlSS1 and OlSS2 from stages 7 to 14 and expression in the pistils was determined from stages 9 to 14 as described by Zhang and Zoe (2009) for O. sativa. Total RNA was isolated from O. longistaminata using an Eastep® Super Total RNA Extraction Kit (Promega, Shanghai, China), with first-strand cDNA being synthesized from 1 μg of the isolated RNA using a PrimeScript RT Reagent Kit with gDNA Eraser (TaKaRa BIO, Shiga, Japan).
RT-PCR and qRT-PCR Analysis
The cDNAs of roots, stems, leaves, stamens, and pistils of O. longistaminata were used as templates for RT-PCR assays. RT-PCR and qRT-PCR amplifications were performed using the following primer pairs: OlSS1-1-F and OlSS1-1-R for OlSS1-1; OlSS1-2-F and OlSS1-2-R for OlSS1-2; OlSS2-1-F and OlSS2-1-R for OlSS2-1; OlSS2-2-F and OlSS2-2-R for OlSS2-2; OlSP-1-F and OlSP-1-R for OlSP-1; and OlSP-2-F and OlSP-2-R for OlSP-2. qRT-PCR analysis was performed using SYBR Premix Ex Taq Kit (TaKaRa BIO) in a Quant Studio 7 Flex real-time PCR system (Applied Biosystems, Foster City, CA, United States) with the following amplification program: initial denaturation at 95°C for 30 s, followed by 40 cycles of denaturation at 95°C for 5 s and primer annealing and extension at 58°C for 34 s. The results were normalized using the relative expression level of Actin2 and analyzed using the 2–Δ Δ Ct method (Livak and Schmittgen, 2001). Three biological replicates were performed for RT-PCR and qRT-PCR analysis. The sequences of the primers used in this study are presented in Supplementary Table 1.
Homologous Cloning of OlSSs and OlSP
Relevant genomic and transcriptomic data for homologous cloning obtained from a previous study on O. longistaminata (Zhang et al., 2015). The cDNA sequences of OlSSs and OlSP were cloned from the transcriptomic database of O. longistaminata by homologous cloning (Zhang et al., 2015). For cDNA cloning, we used the following primers pairs: OlSS1-1-cF and OlSS1-1-cR were used for OlSS1-1; OlSS1-2-cF and OlSS1-2-cR for OlSS1-2; OlSS2-1-cF and OlSS2-1-cR for OlSS2-1; OlSS2-2-cF and OlSS2-2-cR for OlSS2-2; OlSP-1-cF and OlSP-1-cR for OlSP-1; and OlSP-2-cF and OlSP-2-cR for OlSP-2. The products thus amplified were inserted in the pMD19-T vector, and monoclonal sequencing was performed for different haplotypes.
Results
Oryza longistaminata Is a Strictly Self-Incompatible Species
The definitive characteristic of SI is that self-pollination of identical haplotypes results in sterility, whereas pollen is fertile when crossing different haplotypes (Franklin-Tong et al., 1988; Franklin-Tong and Franklin, 2003). In the present study, we grew plants of OlMK68 and OlMK23 in a field to evaluate the SI in O. longistaminata through self-pollination and reciprocal cross-pollination. Although the seed-setting rate of the hybrid (OlMK68/OlMK23) and its reciprocal hybrid was 20.5 ± 3.8 and 26.2 ± 4.7%, respectively (n = 10), in the case of both OlMK23 and OlMK68, self-pollination of plants failed to result in seed set, suggesting strict SI in this species (Table 1 and Supplementary Table 2).
Table 1. Seed-setting rate after self-/cross-pollination in O. longistaminata.
Oryza longistaminata Exhibits Gametophytic Self-Incompatibility
To determine pollen phenotype, we performed staining with aniline blue, which revealed that the pollen of O. longistaminata is able to germinate on the stigma after self-pollination (Figures 1A–D), with germination being observed within 5 min after self-pollination of OlMK68 (Figure 1A), a high rate of germination after 30 min, and the pollen tube reaching the top of the style within 1 h (Figures 1B,C). Subsequently, however, pollen tube growth was inhibited, with the pollen tube appearing to be incapable of passing through the style (Figure 1D). In contrast, pollen growth was consistent in self-pollinated of O. sativa after 5 and 30 min (Figures 1E,F), and the pollen tube was observed to have passed through the style within 1–2 h (Figures 1G,H). These results indicated that although the pollen of O. longistaminata is able to germinate on the stigma after self-pollination, it is incapable of subsequent passage through the style, there implying that this species exhibits GSI.
Figure 1. Pollen germination of Oryza longistaminata and Oryza sativa. (A–D) Self-pollination of O. longistaminata: (A) The pistils of self-pollinated OlMK68 after 5 min, stained with aniline blue solution. (B) The majority of pollen grains had germinated at 0.5 h following self-pollination. (C) The pollen tube reached the top of the style at 1 h after self-pollination. (D) At 2 h after pollination, the pollen tube remained on top of the style and appeared incapable of passing through the style. (E–H) Self-pollination of O. sativa: (E) Pollen began to germinate 5 min after self-pollination. (F) The pollen tube began to elongate at 0.5 h after self-pollination and passed through the style within 1–2 h following cross-pollination (G,H). Bar = 50 μm. The asterisk indicates the germination of pollen grains. Bold arrows indicate pollen tubes in the style.
Oryza longistaminata Self-Incompatibility Determinants Are Linked S-Loci
The corresponding region of the S-locus of L. perenne was found on chromosome 5 of O. sativa, wherein a gene homolog of LpSDUF247 is predicted to encode a DUF247 domain-containing protein (Manzanares et al., 2016). Comparative genomic analysis revealed that a gene located on contig10 of O. longistaminata is syntenic with Os05g0197900 (OsDUF247), named Self-Incompatibility Stamen1 of O. longistaminata (OlSS1) (Figure 2A). OlSS1 encode a DUF247 domain protein, which is similar to LpSDUF247 and considered to be involved in SI (Figure 2B). On the basis of homologous sequence alignment, a gene was predicted to encode a protein containing a DUF247 domain about 19 kb downstream of OlSS1, named Self-Incompatibility Stamen 2 of O. longistaminata (OlSS2) (Figures 2A,B). Previous genomic and transcriptomic sequencing has revealed that both OlSS1 and OlSS2 have two alleles in O. longistaminata (Zhang et al., 2015). RT-PCR assays indicated that alleles OlSS1-1 and OlSS1-2 are expressed primarily in the stamens, whereas the OlSS2-1 and OlSS2-2 alleles are expressed in both stamens and pistils (Figure 2C and Supplementary Figure 1). A defining characteristic of SI is that there should be a close linkage between male and female determinants and expression in stamens and pistils (Franklin-Tong, 2008). Both OlSS1 and OlSS2 show sequence polymorphisms and are expressed in stamens, we speculated that there is a Self-Incompatibility Pistil factor on contig10 of O. longistaminata. Indeed, subsequent sequence polymorphism analysis of a region flanking OlSSs revealed a candidate gene for such a factor, named Self-Incompatibility Pistil factor (OlSP), which may be involved in the SI of O. longistaminata (Figure 2A), given OlSP has a pair of alleles, OlSP-1 and OlSP-2, that are highly and specifically expressed in the pistil (Figure 2C and Supplementary Figure 1). Structural analysis revealed that OlSP encodes an N-terminal YfaZ domain of unknown function (Figure 2B). Consequently, given that OlSSs and OlSP are closely linked and highly expressed in the stamens or pistils of O. longistaminata, we believe that OlSSs and OlSP could be candidate genes controlling SI in this species.
Figure 2. Syntenic and tissue expression of OlSSs and OlSP. (A) Syntenic representation of OlSSs and OlSP in Oryza sativa and Oryza longistaminata. Os05g0197900, which encodes an unknown DUF247 domain protein in O. sativa, corresponds to OlSS1, whereas Os05g0198000 and Os05g0198100 correspond to OlSP and OlSS2 respectively. (B) Analysis of OlSS1, OlSS2, and OlSP protein domains. Both OlSS1 and OlSS2 contain a conserved DUF247 domain, whereas OlSP contains an N-terminal YfaZ domain of unknown function. (C) RT-PCR determination of the tissue-specific expression pattern of OlSSs and OlSP in O. longistaminata. OlSS1-1 and OlSS1-2 are mainly expressed in stamens, whereas OlSS2-1 and OlSS2-2 are expressed in both stamens and pistils, and OlSP-1 and OlSP-2 are highly and specifically expressed in pistils. OlSS1: Self-incompatibility stamen1 from O. longistaminata; OlSS2: Self-incompatibility stamen2 from O. longistaminata; OlSP: Self-Incompatibility Pistil factor from O. longistaminata; O. sativa A05: Oryza sativa chromosome 5.
The alignment of OlSS1-1 and OlSS1-2 amino acid sequences with that of OsDUF247 exhibited similarity level of 80.7 and 69.8%, respectively (Figure 3), whereas the sequences of OlSS2-1 and OlSS2-2 showed lower similarities of 38.9 and 36.9%, respectively (Figure 3). Both OlSS1 and OlSS2 are characterized by conserved regions at the N and C termini. Furthermore, we established that similarities between the amino acid sequences of OlSP1 and OlSP2 and Os05g0198000 are 51.8 and 63.2%, respectively (Figure 4). These findings thus indicate that the OlSS1, OlSS2, and OlSP exhibit sequence polymorphism and can be considered putative SI candidate genes in O. longistaminata.
Figure 3. Amino acid sequence polymorphism of OlSSs. Alignment of the amino acid sequences of OlSS1-1 and OlSS1-2 with that of OsDUF247 revealed similarities of 80.7 and 69.8%, respectively, whereas the corresponding similarities of OlSS2-1 and OlSS2-2 are 38.9 and 36.9%, respectively. Both OlSS1 and OlSS2 showed conserved regions at the N and C termini.
Figure 4. Amino acid sequence polymorphism of OlSP. OlSP-1 and OlSP-2 are the amino acid sequences encoded by the two alleles of OlSP in Oryza longistaminata. The sequence similarity between OlSP-1 and OlSP-2 and Os05g0198000 is 51.8 and 63.2%, respectively.
OlSSs and OlSP Expression Patterns
The expression levels of OlSS1, OlSS2, and OlSP at different development stages of stamen and pistil were analyzed by qRT-PCR assay. The expression of OlSS1-1 was down-regulated during all developmental stages of the stamens, whereas the expression of OlSS1-2 was up-regulated in stages 7–9 and thereafter gradually down-regulated in stages 9–14 (Figure 5A). Interestingly, the expression OlSS2 in stamens was found to show a pattern similar to that of OlSS1, with the down-regulated expression of OlSS2-1 started commencing from stage 10 (Figure 5B). Of the two OlSS2 alleles, whereas OlSS2-2 was up-regulated during pistil development but the expression of OlSS2-1 no significant change (Figure 5C). Moreover, both OlSP-1 and OlSP-2 were rapidly up-regulated during pistil development, with highest expression levels being detected at stage 13 (Figure 5D).
Figure 5. The expression pattern of OlSSs and OlSP. (A) Expression profile of OlSS1 from stage 7 to stage 14 in stamens. OlSS1-1 was down-regulated at all stamen developmental stages, whereas OlSS1-2 was up-regulated at stages 7–9, and gradually down-regulated from stages 9 to 14. (B) The expression pattern of OlSS2 from stage 7 to 14 in stamens. The down-related expression of OlSS2-1 commenced at stage 10. (C) The expression pattern of OlSS2 in pistils. OlSS2-2 up-regulated during pistil development, whereas we detected no significant changes in the expression of OlSS2-1. (D) The expression profile of OlSP in pistils. OlSP-1 and OlSP-2 were up-regulated in pistils. (E) The expression profile of OlSP-1 in pistils after self-/cross-pollination. The down-regulated expression of OlSP-1 commenced 5 min after self-pollination, and reached the highest level at 1 h after cross-pollination. (F) The expression profile of OlSP-2 in pistils after self-/cross-pollination. OlSP-2 showed significant changes in expression following self-pollination, but was up-regulated after cross-pollination, attaining the highest level after 1 h. (G) The expression profile of OlSS2-1 in pistils after self-/cross-pollination. OlSS2-1 was up-regulated within 0.5 h of self-pollination, after which the levels of expression began to decline. In contrast, no significant changes were detected in the expression of OlSS2-1 following cross-pollination. (H) The expression profile of OlSS2-2 in pistils after self-/cross-pollination. OlSS2-2 was up-regulated within 0.5 h of self-pollination, and subsequently down-regulated. Following cross-pollination, the highest level of OlSS2-2 expression was detected within 5 min, after which expression was down-regulated. St, stamen; Pi, pistil; St7 to St14, pollen development from stages 7 to 14; Pi9 to Pi14, pistil development from stages 9 to 14.
Analysis of the expression profiles of OlSP-1, OlSP-2, OlSS2-1, and OlSS2-2 after self-/cross-pollination revealed that the expression of OlSP-1 was highest 5 min after pollination and increased gradually within 1 h after cross-pollination (Figure 5E). Contrastingly, OlSP-2 exhibited no significant change following self-pollination, although showed an expression pattern similar to that of OlSP-1 following cross-pollination (Figure 5F). Expression of OlSS2-1 was found to be highest at 30 min after self-pollination, whereas no significant change following cross-pollination (Figure 5G). OlSS2-2 was up-regulated within 30 min and subsequently down-regulated after self-pollination, whereas following cross-pollination, highest expression levels were detected within 5 min, after which expression was down-regulated (Figure 5H). These observations indicate that whereas OlSS1 and OlSP are expressed in the stamens and pistils, respectively, OlSS2 is expressed in both stamens and pistils, thereby indicating that these three genes are associated with stamen and pistil development. In addition, the results revealed that OlSS1, OlSS2, and OlSP have different expression patterns after self-/cross-pollination.
Discussion
Studies on the genetics of SI in Gramineae were mainly conducted on Secale cereale and Phalaris coerulescens, and have indicated that SI in grass species is under gametophytic control mediated by two unlinked multi-allelic loci referred to as S and Z (Lundqvist, 1954, 1956). Available data indicate that the two-locus SI system is common to all self-incompatible grass species of the subfamily Pooideae, and possibly to all members of the family Gramineae (Connor, 1979). The most significant differences with regards to SI are reciprocal differences in compatibility between two parents (Leach, 1988). In the present study, examination of the compatibility between the two investigated O. longistaminata germplasms (OlMK68 and OlMK23) revealed complete infertility following self-pollination and different seed-setting rates in reciprocal hybrids, indicating strict SI.
In SI, the transmission of signals between the stamens and pistils is dependent on the interaction of S-haplotypes with polymorphic sequences (Franklin-Tong et al., 1988; Franklin-Tong and Franklin, 2003). Therefore, putative specificity determinants should meet the following three criteria suggested by the biology and genetics of SI: linkage to the S-locus, polymorphism between different S-haplotypes, and expression in the pollen or pistil (Franklin-Tong, 2008). In the present study, the sequence polymorphisms and expression patterns of OlSSs and OlSP were in accordance with the characteristics of SI. Moreover, OlSSs and OlSP were found to be closely linked on the O. longistaminata genome, which is consistent with the signaling mechanism of SI.
The primer pairs used in this study were designed based on the allele sequences of OlSSs and OlSP from OlMK68, and on the basis of the tissue-specific expression and expression levels in stamens and pistils at different stages of developmental, we confirmed that OlSSs and OlSP are polymorphic loci. Moreover, qRT-PCR analysis revealed that the alleles of OlSS1 and OlSS2 show identical expression patterns in stamens, thereby indicating the comparable or synergistic functions of OlSS1 and OlSS2. Given that the expression of OlSS1 was gradually down-regulated during the latter stages of pollen maturation, further examination of the expression of this gene at the cellular level will be necessary to more precisely determine whether OlSS1 is expressed in the pollen or in the tapetum. Besides, OlSS2 was also expressed in the pistil, but only the OlSS2-2 allele is up-regulated during pistil development. The reason for this phenomenon could be indictive of the complex mechanism of SI in O. longistaminata, which requires further study. A notable observation in the present study was that pollen on the stigma was unable to enter the style following self-pollination, indicating that either the pollen carries a male SI signal factor and/or that a pistil signal factor is secreted into the style. Although OlSSs and OlSP are considered to be the respective candidate genes for these factors in the SI of O. longistaminata, the mechanisms whereby they contribute to the regulation SI need to be further studied.
Data Availability Statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Author Contributions
FH and XL designed the experiments and wrote the manuscript. XL, SZ, and JZ performed the experiments. GH and LH analyzed the data. All authors have read and agreed to the submitted version of the manuscript.
Funding
This work was funded by Yunnan Postdoctoral Sustentation Fund, China (2020 for XL) and National Natural Science Foundation of China (3U1302264 for FH).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We would like to thank Lin Shao for his contribution in revising the language of our manuscript.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2021.576340/full#supplementary-material
Footnotes
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Keywords: gametophytic, OlSP, OlSS, Oryza longistaminata, self-incompatibility
Citation: Lian X, Zhang S, Huang G, Huang L, Zhang J and Hu F (2021) Confirmation of a Gametophytic Self-Incompatibility in Oryza longistaminata. Front. Plant Sci. 12:576340. doi: 10.3389/fpls.2021.576340
Received: 25 June 2020; Accepted: 15 March 2021;
Published: 31 March 2021.
Edited by:
Kenneth Lee McNally, International Rice Research Institute (IRRI), PhilippinesReviewed by:
Lijun Chai, Huazhong Agricultural University, ChinaMulatu Geleta, Swedish University of Agricultural Sciences, Sweden
Kazuyuki Doi, Nagoya University, Japan
Copyright © 2021 Lian, Zhang, Huang, Huang, Zhang and Hu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Fengyi Hu, hfengyi@ynu.edu.cn