TY - JOUR
T1 - Global RNA interactome of Salmonella discovers a 5′ UTR sponge for the MicF small RNA that connects membrane permeability to transport capacity
AU - Matera, Gianluca
AU - Altuvia, Yael
AU - Gerovac, Milan
AU - El Mouali, Youssef
AU - Margalit, Hanah
AU - Vogel, Jörg
N1 - Publisher Copyright: © 2021 The Author(s)
PY - 2022/2/3
Y1 - 2022/2/3
N2 - The envelope of Gram-negative bacteria is a vital barrier that must balance protection and nutrient uptake. Small RNAs are crucial regulators of the envelope composition and function. Here, using RIL-seq to capture the Hfq-mediated RNA-RNA interactome in Salmonella enterica, we discover envelope-related riboregulators, including OppX. We show that OppX acts as an RNA sponge of MicF sRNA, a prototypical porin repressor. OppX originates from the 5′ UTR of oppABCDF, encoding the major inner-membrane oligopeptide transporter, and sequesters MicF's seed region to derepress the synthesis of the porin OmpF. Intriguingly, OppX operates as a true sponge, storing MicF in an inactive complex without affecting its levels or stability. Conservation of the opp-OppX-MicF-ompF axis in related bacteria suggests that it serves an important mechanism, adjusting envelope porosity to specific transport capacity. These data also highlight the resource value of this Salmonella RNA interactome, which will aid in unraveling RNA-centric regulation in enteric pathogens.
AB - The envelope of Gram-negative bacteria is a vital barrier that must balance protection and nutrient uptake. Small RNAs are crucial regulators of the envelope composition and function. Here, using RIL-seq to capture the Hfq-mediated RNA-RNA interactome in Salmonella enterica, we discover envelope-related riboregulators, including OppX. We show that OppX acts as an RNA sponge of MicF sRNA, a prototypical porin repressor. OppX originates from the 5′ UTR of oppABCDF, encoding the major inner-membrane oligopeptide transporter, and sequesters MicF's seed region to derepress the synthesis of the porin OmpF. Intriguingly, OppX operates as a true sponge, storing MicF in an inactive complex without affecting its levels or stability. Conservation of the opp-OppX-MicF-ompF axis in related bacteria suggests that it serves an important mechanism, adjusting envelope porosity to specific transport capacity. These data also highlight the resource value of this Salmonella RNA interactome, which will aid in unraveling RNA-centric regulation in enteric pathogens.
KW - 5' Untranslated Regions
KW - Biological Transport
KW - Cell Membrane/genetics
KW - Escherichia coli Proteins/genetics
KW - Gene Expression Regulation, Bacterial
KW - Host Factor 1 Protein/genetics
KW - Host-Pathogen Interactions
KW - Permeability
KW - Porins/genetics
KW - RNA, Bacterial/genetics
KW - RNA-Seq
KW - Salmonella enterica/genetics
UR - http://www.scopus.com/inward/record.url?scp=85123693602&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.molcel.2021.12.030
DO - https://doi.org/10.1016/j.molcel.2021.12.030
M3 - مقالة
C2 - 35063132
SN - 1097-2765
VL - 82
SP - 629-644.e4
JO - Molecular Cell
JF - Molecular Cell
IS - 3
ER -