Name: | Description: | Size: | Format: | |
---|---|---|---|---|
223.38 KB | Adobe PDF |
Advisor(s)
Abstract(s)
An inexpensive and rapid RNA extraction protocol for brown algae and seagrasses is presented, based on homogenization in a simple CTAB buffer and selective precipitation of RNA with lithium chloride. The protocol avoids the use of toxic chaotropic agents and phenol; high concentrations of dithiothreitol are used to inhibit RNase activity and to prevent oxidative cross-linking of nucleic acids by phenolics. A relatively high throughput of about 100 samples in 24 h can be achieved for, for example, Northern analysis. Yields of 50–200 µg g−1 fresh weight are comparable with those obtained for higher plants using commercially available kits. Tests of the extraction procedure demonstrate that high quality, intact RNA can be obtained from a variety of lyophilized brown algal tissues, even after prolonged storage at room temperature. Lyophilization is therefore suggested as an alternative to freezing tissue at −70°C to −80°C. The RNA obtained was used directly in several downstream applications to detect Fucus plastid-encoded transcripts by RNA-labelling, RT-PCR and Northern analysis.
Description
Keywords
Brown algae Fucus Lyophilization Plastid gene expression
Citation
Pearson, G.A.; Lago-Leston, A.; Valente, M.; Serrão, E.A.Simple and rapid RNA extraction from freeze-dried tissue of brown algae and seagrasses, European Journal of Phycology, 41, 1, 97-104, 2006.
Publisher
Taylor & Francis