| Literature DB >> 31761536 |
Margaret L Rodgers1, Sarah A Woodson2.
Abstract
The synthesis of new ribosomes begins during transcription of the rRNA and is widely assumed to follow an orderly 5' to 3' gradient. To visualize co-transcriptional assembly of ribosomal protein-RNA complexes in real time, we developed a single-molecule platform that simultaneously monitors transcription and protein association with the elongating transcript. Unexpectedly, the early assembly protein uS4 binds newly made pre-16S rRNA only transiently, likely due to non-native folding of the rRNA during transcription. Stable uS4 binding became more probable only in the presence of additional ribosomal proteins that bind upstream and downstream of protein uS4 by allowing productive assembly intermediates to form earlier. We propose that dynamic sampling of elongating RNA by multiple proteins overcomes heterogeneous RNA folding, preventing assembly bottlenecks and initiating assembly within the transcription time window. This may be a common feature of transcription-coupled RNP assembly.Entities:
Keywords: 16S RNA; 30S ribosome; RNP; co-transcriptional RNA folding; co-transcriptional RNP assembly; colocalization single-molecule spectroscopy; ribonucleoprotein assembly; ribosome biogenesis; single-molecule fluorescence; transcription
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Year: 2019 PMID: 31761536 PMCID: PMC6886681 DOI: 10.1016/j.cell.2019.11.007
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582