期刊
NATURE COMMUNICATIONS
卷 9, 期 -, 页码 -出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-018-07423-3
关键词
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资金
- Swiss National Science Foundation (SNF) [P2EZP3-152131, P300PA-160978]
- Human Frontier Science Program [LT000628/2015-L]
- NIH [R01 GM053757, R01 GM051266]
- NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM053757, R37GM053757] Funding Source: NIH RePORTER
Cellular protein-RNA complexes assemble on nascent transcripts, but methods to observe transcription and protein binding in real time and at physiological concentrations are not available. Here, we report a single-molecule approach based on zero-mode waveguides that simultaneously tracks transcription progress and the binding of ribosomal protein S15 to nascent RNA transcripts during early ribosome biogenesis. We observe stable binding of S15 to single RNAs immediately after transcription for the majority of the transcripts at 35 degrees C but for less than half at 20 degrees C. The remaining transcripts exhibit either rapid and transient binding or are unable to bind S15, likely due to RNA misfolding. Our work establishes the foundation for studying transcription and its coupled co-transcriptional processes, including RNA folding, ligand binding, and enzymatic activity such as in coupling of transcription to splicing, ribosome assembly or translation.
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