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The δ subunit and NTPase HelD institute a two-pronged mechanism for RNA polymerase recycling

H.-H. Pei, T. Hilal, Z. A. Chen, Y.-H. Huang, Y. Gao, N. Said, B. Loll, J. Rappsilber, G. A. Belogurov, I. Artsimovitch and M. C. Wahl – 2020

Cellular RNA polymerases (RNAPs) can become trapped on DNA or RNA, threatening genome stability and limiting free enzyme pools, but how RNAP recycling into active states is achieved remains elusive. In Bacillus subtilis, the RNAP δ subunit and NTPase HelD have been implicated in RNAP recycling. We structurally analyzed Bacillus subtilis RNAP-δ-HelD complexes. HelD has two long arms: a Gre cleavage factor-like coiled-coil inserts deep into the RNAP secondary channel, dismantling the active site and displacing RNA, while a unique helical protrusion inserts into the main channel, prying the β and β′ subunits apart and, aided by δ, dislodging DNA. RNAP is recycled when, after releasing trapped nucleic acids, HelD dissociates from the enzyme in an ATP-dependent manner. HelD abundance during slow growth and a dimeric (RNAP-δ-HelD)2 structure that resembles hibernating eukaryotic RNAP I suggest that HelD might also modulate active enzyme pools in response to cellular cues.

Titel
The δ subunit and NTPase HelD institute a two-pronged mechanism for RNA polymerase recycling
Verfasser
H.-H. Pei, T. Hilal, Z. A. Chen, Y.-H. Huang, Y. Gao, N. Said, B. Loll, J. Rappsilber, G. A. Belogurov, I. Artsimovitch and M. C. Wahl
Datum
2020
Kennung
DOI:10.1038/s41467-020-20159-3
Zitierweise
Nat Commun 2020, 11 (1), 6418
Sprache
eng
Art
Text