(p)ppGpp controls stringent factors by exploiting antagonistic allosteric coupling between catalytic domains.

Roghanian M, Van Nerom K, Takada H, Caballero-Montes J, Tamman H, Kudrin P, Talavera A, Dzhygyr I, Ekström S, Atkinson GC, Garcia-Pino A, Hauryliuk V

Mol. Cell 81 (16) 3310-3322.e6 [2021-08-19; online 2021-08-21]

Amino acid starvation is sensed by Escherichia coli RelA and Bacillus subtilis Rel through monitoring the aminoacylation status of ribosomal A-site tRNA. These enzymes are positively regulated by their product-the alarmone nucleotide (p)ppGpp-through an unknown mechanism. The (p)ppGpp-synthetic activity of Rel/RelA is controlled via auto-inhibition by the hydrolase/pseudo-hydrolase (HD/pseudo-HD) domain within the enzymatic N-terminal domain region (NTD). We localize the allosteric pppGpp site to the interface between the SYNTH and pseudo-HD/HD domains, with the alarmone stimulating Rel/RelA by exploiting intra-NTD autoinhibition dynamics. We show that without stimulation by pppGpp, starved ribosomes cannot efficiently activate Rel/RelA. Compromised activation by pppGpp ablates Rel/RelA function in vivo, suggesting that regulation by the second messenger (p)ppGpp is necessary for mounting an acute starvation response via coordinated enzymatic activity of individual Rel/RelA molecules. Control by (p)ppGpp is lacking in the E. coli (p)ppGpp synthetase SpoT, thus explaining its weak synthetase activity.

Structural Proteomics [Collaborative]

PubMed 34416138

DOI 10.1016/j.molcel.2021.07.026

Crossref 10.1016/j.molcel.2021.07.026

pii: S1097-2765(21)00595-5


Publications 7.1.2