Abstract
RNA isolation is essential to study gene expression at the molecular level. However, RNA isolation is difficult in organisms (plants and algae) that contain large amounts of polysaccharides, which co-precipitate with RNA. Currently, there is no commercial kit available, specifically for the isolation of high-quality RNA from these organisms. Furthermore, because of the large amounts of polysaccharides, the common protocols for RNA isolation usually result in poor yields when applied to algae. Here we describe a simple method for RNA isolation from the marine red macroalga Gracilaria tenuistipitata var. liui Zhang et Xia (Rhodophyta), which can be applied to other plants and algae.
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Abbreviations
- DEPC:
-
Diethylpyrocarbonate
- ETOH:
-
Ethanol
- GHCL:
-
guanidinium Hydrochloride extraction buffer
- HMW-PEG:
-
High molecular weight polyethylene glycol
- KOAc:
-
Potassium acetate
- PVP:
-
Polyvinylpyrrolidone
- RT-PCR:
-
Reverse transcription coupled with polymerase chain reaction
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This research was supported by FAPESP (Fundação de Apoio a Pesquisa do Estado de São Paulo).
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Dos Reis Falcão, V., Pedroso Tonon, A., Cabral Oliveira, M. et al. RNA Isolation method for polysaccharide rich algae: agar producing Gracilaria tenuistipitata (Rhodophyta). J Appl Phycol 20, 9–12 (2008). https://doi.org/10.1007/s10811-007-9174-7
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DOI: https://doi.org/10.1007/s10811-007-9174-7