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Dalla Rizza, J.

Publications and source records attributed to Dalla Rizza, J..

2 recordsLinked to original sources

Bacterial targeting of host paraspeckles uncovers a new SFPQ-based regulation

Nuclear functions are key in protecting cells against infections, yet intracellular pathogens like Legionella pneumophila can exploit these mechanisms to survive. We characterized a L. pneumophila protein, LpDot1, which shares sequence similarity with the eukaryotic catalytic domain of the histone methyltransferase DOT1. Structure determination, together with biochemical and biophysical analyses, revealed that LpDot1 methylates non-histone nuclear proteins, notably the splicing factor proline-glutamine rich protein (SFPQ). Importantly, LpDot1 targets the previously uncharacterized K518, located on an important structural motif of SFPQ, therefore impairing its dimerization in vitro. During infection, L. pneumophila modulates SFPQ abundance and activities in a LpDot1-dependent manner, thereby hijacking paraspeckle organization and the host cell splicing machinery, leading to alternative splice variants of infection related genes such as NF-kB2 and CD45. To our knowledge, this is the first report of a bacterial effector directly modifying paraspeckle dynamics, providing new insight into previously uncharacterized eukaryotic regulatory pathways.

microbiology↗

Engineering directional phosphoryl flow enables programmable signaling dynamics in bacteria

Cells must make critical decisions by integrating information from a constantly changing environment to ensure their survival. They rely on intricate signaling networks to detect external and internal cues to trigger specific responses, yet these systems are generally viewed as components wired with simpler linear connections. Bacterial phosphorelay systems offer a versatile framework for studying more complex connections and engineering new biological circuits. Here, using the well-studied Bacillus subtilis sporulation phosphorelay, we demonstrate that the directionality of information flow can be reprogrammed to generate different dynamic responses. We show that phosphoryl-transfer reversibility is an evolvable trait encoded in conserved, surface-exposed motifs of two-component system proteins. Unidirectional phosphoryl-transfer generates a short-term information storage mechanism, enabling signal integration over time and allowing phosphatases, acting at different levels, to produce different outcomes. In contrast, a bidirectional system enhanced the action of phosphatase activity early in the pathway. The ability to control phosphoryl-transfer equilibria opens exciting avenues for designing sophisticated synthetic signaling systems with enhanced decision-making capabilities.

systems biology↗