Quantitative comparison of DNA detection by GFP-lac repressor tagging, fluorescence in situ hybridization and immunostaining
Autor: | Roland Eils, Il Han Kim, Boris Knerr, Steffen Dietzel, Karl Rohr, Jens Nagel, Simone Otten |
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Jazyk: | angličtina |
Rok vydání: | 2007 |
Předmět: |
Recombinant Fusion Proteins
lcsh:Biotechnology Cell Green Fluorescent Proteins Repressor Biology Lac repressor Green fluorescent protein chemistry.chemical_compound Mice Cell Line Tumor lcsh:TP248.13-248.65 medicine Image Processing Computer-Assisted Animals In Situ Hybridization Fluorescence medicine.diagnostic_test DNA Molecular biology Immunohistochemistry Repressor Proteins medicine.anatomical_structure chemistry Immunostaining Fluorescence in situ hybridization Biotechnology Research Article |
Zdroj: | BMC Biotechnology, Vol 7, Iss 1, p 92 (2007) BMC Biotechnology |
ISSN: | 1472-6750 |
Popis: | Background GFP-fusion proteins and immunostaining are methods broadly applied to investigate the three-dimensional organization of cells and cell nuclei, the latter often studied in addition by fluorescence in situ hybridization (FISH). Direct comparisons of these detection methods are scarce, however. Results We provide a quantitative comparison of all three approaches. We make use of a cell line that contains a transgene array of lac operator repeats which are detected by GFP-lac repressor fusion proteins. Thus we can detect the same structure in individual cells by GFP fluorescence, by antibodies against GFP and by FISH with a probe against the transgene array. Anti-GFP antibody detection was repeated after FISH. Our results show that while all four signals obtained from a transgene array generally showed qualitative and quantitative similarity, they also differed in details. Conclusion Each of the tested methods revealed particular strengths and weaknesses, which should be considered when interpreting respective experimental results. Despite the required denaturation step, FISH signals in structurally preserved cells show a surprising similarity to signals generated before denaturation. |
Databáze: | OpenAIRE |
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