Abstract

Polyploidy, or whole-genome duplication, is a common speciation mechanism in plants. An important barrier to polyploid establishment is a lack of compatible mates. Because self-compatibility alleviates this problem, it has long been hypothesized that there should be an association between polyploidy and self-compatibility (SC), but empirical support for this prediction is mixed. Here, we investigate whether the molecular makeup of the Brassicaceae self-incompatibility (SI) system, and specifically dominance relationships among S-haplotypes mediated by small RNAs, could facilitate loss of SI in allopolyploid crucifers. We focus on the allotetraploid species Capsella bursa-pastoris, which formed ~300 kya by hybridization and whole-genome duplication involving progenitors from the lineages of Capsella orientalis and Capsella grandiflora. We conduct targeted long-read sequencing to assemble and analyze eight full-length S-locus haplotypes, representing both homeologous subgenomes of C. bursa-pastoris. We further analyze small RNA (sRNA) sequencing data from flower buds to identify candidate dominance modifiers. We find that C. orientalis-derived S-haplotypes of C. bursa-pastoris harbor truncated versions of the male SI specificity gene SCR and express a conserved sRNA-based candidate dominance modifier with a target in the C. grandiflora-derived S-haplotype. These results suggest that pollen-level dominance may have facilitated loss of SI in C. bursa-pastoris. Finally, we demonstrate that spontaneous somatic tetraploidization after a wide cross between C. orientalis and C. grandiflora can result in production of self-compatible tetraploid offspring. We discuss the implications of this finding on the mode of formation of this widespread weed.

Highlights

  • In line with a previous study (Bachmann et al 2019) we found that all C. bursa-pastoris B S-haplotypes clustered together and harbored C. orientalis-derived mutations that are expected to result in the expression of a truncated and likely nonfunctional SCR protein

  • We further found that all our C. bursa-pastoris samples harbored very similar A Shaplogroup sequences, and polymorphism was very low at SRK of both subgenomes

  • While low polymorphism at the B S-haplogroup might be expected given the limited diversity in the parental species C. orientalis (Douglas et al 2015), limited polymorphism at the C. bursa-pastoris A S-haplogroup is more surprising given the high number of S-haplotypes currently segregating in C. grandiflora (Guo et al 2009)

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Summary

Present address

Each S-haplotype harbors multiple S-linked F-box genes that can detoxify several different maternal SRNases, but not their own In this system, the presence of two S-alleles in unreduced pollen grains can allow detoxification of any maternal S-RNase and immediately leads to self-compatibility in polyploids (Kubo et al 2010). The SC species C. orientalis harbors a dominant and nonfunctional S-haplotype with a coding frameshift mutation in the SCR gene, which is shared with C. bursapastoris B (Bachmann et al 2019) This suggests that C. orientalis was SC when it gave rise to C. bursa-pastoris. If the C. bursa-pastoris A subgenome S-haplotype from the C. grandiflora lineage is more recessive than the B-haplotype from the C. orientalis lineage, it is possible that the newly formed allotetraploid C. bursa-pastoris was immediately SC Such instant SC might have facilitated establishment of the new allopolyploid.

Materials and methods
Results
A CbpWESE
A CbpWEDE 5’ ATCAACTTCCTTTTGGTTTTGATT 3’
Discussion
Compliance with ethical standards
Full Text
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