A simple non-toxic ethylene carbonate fluorescence in situ hybridization (EC-FISH) for simultaneous detection of repetitive DNA sequences and fluorescent bands in plants
Autor: | Hieronim Golczyk |
---|---|
Rok vydání: | 2019 |
Předmět: |
0106 biological sciences
0301 basic medicine Indoles rDNA Plant Science Tradescantia DNA Ribosomal 01 natural sciences Fluorescence 03 medical and health sciences chemistry.chemical_compound Heterochromatin medicine Repeated sequence In Situ Hybridization Fluorescence Ethylene carbonate Repetitive Sequences Nucleic Acid Base Sequence medicine.diagnostic_test biology Fluorescence in situ hybridization Hybridization probe Chromosome Dioxolanes Karyotype Cell Biology General Medicine Plants Chromosome DAPI banding biology.organism_classification 030104 developmental biology Biochemistry chemistry Original Article DNA Probes 010606 plant biology & botany |
Zdroj: | Protoplasma |
ISSN: | 1615-6102 0033-183X |
DOI: | 10.1007/s00709-019-01345-7 |
Popis: | The major drawbacks of standard plant fluorescence in situ hybridization (FISH) designed for double-stranded DNA probes include requirement for experimentally determined heat denaturation of chromosomes at high temperatures and at least overnight hybridization. Consequently, processing with chromosomal preparations may easily result in heat-induced deterioration of chromosomal structural details, is time-consuming, and involves the use of toxic formamide and formaldehyde. Here, I have described a simple and appealing non-toxic procedure with ethylene carbonate (EC)—a formamide-substituting solvent and double-stranded repetitive DNA probes. Applying EC as a component of the hybridization solution at 46 °C not only allowed successful overnight hybridization but also gave a possibility to reduce the hybridization time to 3 h, hence converting the technique into a 1-day procedure. Importantly, the EC-FISH tended to preserve well chromosome structural details, e.g., DAPI-positive bands, thus facilitating simultaneous FISH mapping and chromosome banding on the same slide. The procedure requires no formaldehyde and RNA-se treatment of chromosomes, and no heat denaturation of chromosomal DNA. The key condition is to obtain high-quality cytoplasm-free preparations. The method was reproducible in all the plants studied (Allium, Nigella, Tradescantia, Vicia), giving a species-specific signal pattern together with clear DAPI bands on chromosomes. The procedure described here is expected to give a positive stimulus for improving gene-mapping approaches in plants. Electronic supplementary material The online version of this article (10.1007/s00709-019-01345-7) contains supplementary material, which is available to authorized users. |
Databáze: | OpenAIRE |
Externí odkaz: |