Escherichia coli NusG Links the Lead Ribosome with the Transcription Elongation Complex

Summary

It has been known for more than 50 years that transcription and translation are physically coupled in bacteria, but whether or not this coupling may be mediated by the two-domain protein N-utilization substance (Nus) G in Escherichia coli is still heavily debated. Here, we combine integrative structural biology and functional analyses to provide conclusive evidence that NusG can physically link transcription with translation by contacting both RNA polymerase and the ribosome. We present a cryo-electron microscopy structure of a NusG:70S ribosome complex and nuclear magnetic resonance spectroscopy data revealing simultaneous binding of NusG to RNAP and the intact 70S ribosome, providing the first direct structural evidence for NusG-mediated coupling. Furthermore, in vivo reporter assays show that recruitment of NusG occurs late in transcription and strongly depends on translation. Thus, our data suggest that coupling occurs initially via direct RNAP:ribosome contacts and is then mediated by NusG.

Graphical Abstract

Highlights

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  NusG can contact RNAP and lead ribosome simultaneously

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  NusG recruitment occurs late during transcription and depends on translation

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  NusG-mediated coupling happens during late translation

Abstract

Biochemistry; Biochemistry Methods; Structural Biology; Three-Dimensional Reconstruction of Biomolecular Structures