TY - JOUR
T1 - Formation of a membraneless compartment regulates bacterial virulence
AU - Aroeti, Lior
AU - Elbaz, Netanel
AU - Faigenbaum-Romm, Raya
AU - Yakovian, Oren
AU - Altuvia, Yael
AU - Argaman, Liron
AU - Katsowich, Naama
AU - Bejerano-Sagie, Michal
AU - Ravins, Miriam
AU - Margalit, Hanah
AU - Ben-Yehuda, Sigal
AU - Rosenshine, Ilan
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - The RNA-binding protein CsrA regulates the expression of hundreds of genes in several bacterial species, thus controlling virulence and other processes. However, the outcome of the CsrA-mRNA interactions is modulated by competing small RNAs and other factors through mechanisms that are only partially understood. Here, we show that CsrA accumulates in a dynamic membraneless compartment in cells of E. coli and other pathogenic species. In addition to CsrA, the compartment contains components of the RNA-degrading complex (degradosome), regulatory small RNAs, and selected mRNAs. Formation of the compartment is associated with a switch between promoting and repressing virulence gene expression by CsrA. We suggest that similar CsrA switches may be widespread in diverse bacteria.
AB - The RNA-binding protein CsrA regulates the expression of hundreds of genes in several bacterial species, thus controlling virulence and other processes. However, the outcome of the CsrA-mRNA interactions is modulated by competing small RNAs and other factors through mechanisms that are only partially understood. Here, we show that CsrA accumulates in a dynamic membraneless compartment in cells of E. coli and other pathogenic species. In addition to CsrA, the compartment contains components of the RNA-degrading complex (degradosome), regulatory small RNAs, and selected mRNAs. Formation of the compartment is associated with a switch between promoting and repressing virulence gene expression by CsrA. We suggest that similar CsrA switches may be widespread in diverse bacteria.
UR - http://www.scopus.com/inward/record.url?scp=105003311990&partnerID=8YFLogxK
U2 - 10.1038/s41467-025-58829-9
DO - 10.1038/s41467-025-58829-9
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C2 - 40268935
AN - SCOPUS:105003311990
SN - 2041-1723
VL - 16
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 3834
ER -