Barley germination dissection: wfg-24h

Sample Details

Whole Fixed Grain, 24-hour

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Data-set Details

Isolated barley (Hordeum vulgare L.) aleurone layers have been widely used as a model system for studying gene expression and hormonal regulation in germinating cereal grains. A serious technological limitation of this approach has been the inability to confidently extrapolate conclusions obtained from isolated tissues back to the whole grain, where the co-location of several living and non-living tissues results in complex tissue-tissue interactions and regulatory pathways coordinated across the multiple tissues. Here, we have developed methods for isolating fragments of aleurone, starchy endosperm, embryo, scutellum, pericarp-testa, husk and crushed cell layers from germinated grain. An important step in the procedure involves the rapid fixation of the intact grain to freeze the transcriptional activity of individual tissues while dissection is effected for subsequent transcriptomic analyses. The developmental profiles of 19,611 gene transcripts were precisely defined in the purified tissues and in whole grain during the first 24 hours of germination by RNA-seq. Spatial and temporal patterns of transcription were validated against well-defined data on enzyme activities both in whole grain and in isolated tissues. Transcript profiles of genes involved in mitochondrial assembly and function were used to validate the very early stages of germination, while the profiles of genes involved in starch and cell wall mobilization matched existing data on activities of corresponding enzymes. The data will be broadly applicable for the interrogation of co-expression and differential expression patterns and for the identification of transcription factors that are important in the early stages of grain and seed germination.

Publication: doi.org/10.1111/tpj.13600

Research Data Australia: https://researchdata.ands.org.au/developmental-profiles-19611-rna-seq/938768