Detection of RNA-DNA hybrids by immunostaining in meiotic nuclei of Saccharomyces cerevisiae
RNA transcripts can anneal with template DNA strands to form RNA-DNA hybrids (or R-loops if the non-template DNA strands exist), which play a variety of roles in many physiological processes. Here, we provide an accessible and reproducible approach for immunofluorescent staining of RNA-DNA hybrids w...
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Veröffentlicht in: | STAR protocols 2022-06, Vol.3 (2), p.101325-101325, Article 101325 |
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Sprache: | eng |
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Zusammenfassung: | RNA transcripts can anneal with template DNA strands to form RNA-DNA hybrids (or R-loops if the non-template DNA strands exist), which play a variety of roles in many physiological processes. Here, we provide an accessible and reproducible approach for immunofluorescent staining of RNA-DNA hybrids with the S9.6 antibody in spread meiotic nuclei of Saccharomyces cerevisiae. This protocol allows the examination of RNA-DNA hybrids as clearly distinguishable foci and the colocalizations of RNA-DNA hybrids with other proteins.
For complete details on the use and execution of this protocol, please refer to Yang et al. (2021).
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•Protocol for sensitive detection of RNA-DNA hybrids in yeast meiotic nuclei•Detailed description of optimized meiotic synchronization and chromosome spread•General protocol for detection of RNA-DNA hybrids and interested proteins
Publisher's note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics.
RNA transcripts can anneal with template DNA strands to form RNA-DNA hybrids (or R-loops if the non-template DNA strands exist), which play a variety of roles in many physiological processes. Here, we provide an accessible and reproducible approach for immunofluorescent staining of RNA-DNA hybrids with the S9.6 antibody in spread meiotic nuclei of Saccharomyces cerevisiae. This protocol allows the examination of RNA-DNA hybrids as clearly distinguishable foci and the colocalizations of RNA-DNA hybrids with other proteins. |
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ISSN: | 2666-1667 2666-1667 |
DOI: | 10.1016/j.xpro.2022.101325 |