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XXII. BIOCHEMICKÝ ZJAZD - Jesseniova lekárska fakulta

XXII. BIOCHEMICKÝ ZJAZD - Jesseniova lekárska fakulta

XXII. BIOCHEMICKÝ ZJAZD - Jesseniova lekárska fakulta

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Posters<br />

31.<br />

CHaraCTERIZATION OF a GENE ENCODING a SMALL REGULATORY RPOE<br />

– DEPENDENT RNA IN SALMoneLLA enTerICA SEROvar TYPHIMURIUM<br />

Dagmar Homerová, Bronislava Řežuchová, Henrieta Škovierová and Ján Kormanec<br />

Institute of Molecular Biology, Slovak Academy of Sciences, Bratislava<br />

Gene regulation of bacteria is a complex process in which proteins have been believed<br />

as the only relevant regulators for a long time. In recent years, the family of small noncoding<br />

RNA (sRNA) with the important role especially in post-transcription control<br />

was described. Enterobacterial pathogen Salmonella enterica serovar Typhimurium<br />

(S. Typhimurium) is an attractive model for studying sRNAs, since the research could<br />

clarify many processes affecting the regulation of bacterial pathogenicity. So far, more<br />

than 70 sRNAs with various roles in control of gene expression have been identified in S.<br />

Typhimurium. Among them, small antisense RNA MicA, activated by sigma factor RpoE,<br />

strongly represses the mRNAs of two porins, OmpA and LamB. To understand the role<br />

of MicA we have investigated its expression and role in virulence of S. Typhimurium. In<br />

vitro transcriptional analysis revealed presence of a single promoter, micAp, with the<br />

high similarity with the consensus RpoE promoter sequence showing clear dependence<br />

upon this sigma factor. Activity of micAp increased towards stationary phase and was<br />

induced by several stresses including heat shock, cold shock, acid stress, oxidative stress,<br />

ethanol, polymixin B, and by degS-specific stress elicited by unfolded C-terminal outer<br />

membrane protein OmpA. Lack of micA elicited an RpoE-dependent envelope stress<br />

response. Although in vitro phenotypic analysis revealed no significant differences between<br />

wild type and micA mutant strains, in vivo studies showed that the micA mutant<br />

is more virulent in the mouse model.<br />

Ackowledgement: This work was supported by the VEGA grant 2/0104/09 from Slovak<br />

Academy of Sciences.<br />

<strong>XXII</strong>. Biochemistry Congress, Martin<br />

149

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