Isolation of High Purity Tissues from Developing Barley Seeds
Language English Country United States Media electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Video-Audio Media
PubMed
33165320
DOI
10.3791/61681
Knihovny.cz E-resources
- MeSH
- Endosperm chemistry growth & development MeSH
- Hordeum chemistry genetics growth & development MeSH
- Ploidies * MeSH
- Seeds chemistry genetics growth & development MeSH
- Publication type
- Video-Audio Media MeSH
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Understanding the mechanisms regulating the development of cereal seeds is essential for plant breeding and increasing yield. However, the analysis of cereal seeds is challenging owing to the minute size, the liquid character of some tissues, and the tight inter-tissue connections. Here, we demonstrate a detailed protocol for dissection of the embryo, endosperm, and seed maternal tissues at early, middle, and late stages of barley seed development. The protocol is based on a manual tissue dissection using fine-pointed tools and a binocular microscope, followed by ploidy analysis-based purity control. Seed maternal tissues and embryos are diploid, while the endosperm is triploid tissue. This allows the monitoring of sample purity using flow cytometry. Additional measurements revealed the high quality of RNA isolated from such samples and their usability for high-sensitivity analysis. In conclusion, this protocol describes how to practically dissect pure tissues from developing grains of cultivated barley and potentially also other cereals.
References provided by Crossref.org
Core promoterome of barley embryo
The transcriptome landscape of developing barley seeds
Endopolyploidy Variation in Wild Barley Seeds across Environmental Gradients in Israel