4.8 Article

Single seeds exhibit transcriptional heterogeneity during secondary dormancy induction

Journal

PLANT PHYSIOLOGY
Volume 190, Issue 1, Pages 211-225

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/plphys/kiac265

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Funding

  1. Foundation for Polish Science [TEAM POIR.04.04.00-00-3C97/16]
  2. National Science Centre, Poland [SONATA BIS UMO-2018/30/E/NZ1/00354]
  3. National Science Centre grant [OPUS UMO-2018/31/B/NZ3/03363]

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Seeds have strong resilience and adopt a bet-hedging strategy to persist in unfavorable conditions. By using single-seed RNA sequencing, the transcriptional heterogeneity of seeds and the induction of secondary dormancy can be elucidated.
Seeds are highly resilient to the external environment, which allows plants to persist in unpredictable and unfavorable conditions. Some plant species have adopted a bet-hedging strategy to germinate a variable fraction of seeds in any given condition, and this could be explained by population-based threshold models. Here, in the model plant Arabidopsis (Arabidopsis thaliana), we induced secondary dormancy (SD) to address the transcriptional heterogeneity among seeds that leads to binary germination/nongermination outcomes. We developed a single-seed RNA-seq strategy that allowed us to observe a reduction in seed transcriptional heterogeneity as seeds enter stress conditions, followed by an increase during recovery. We identified groups of genes whose expression showed a specific pattern through a time course and used these groups to position the individual seeds along the transcriptional gradient of germination competence. In agreement, transcriptomes of dormancy-deficient seeds (mutant of DELAY OF GERMINATION 1) showed a shift toward higher values of the germination competence index. Interestingly, a significant fraction of genes with variable expression encoded translation-related factors. In summary, interrogating hundreds of single-seed transcriptomes during SD-inducing treatment revealed variability among the transcriptomes that could result from the distribution of population-based sensitivity thresholds. Our results also showed that single-seed RNA-seq is the method of choice for analyzing seed bet-hedging-related phenomena. Single-seed RNA sequencing enables analysis of gene expression variability and elucidates secondary dormancy induction as a potential bet-hedging strategy.

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