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A σD-dependent antisense transcript modulates expression of the cyclic-di-AMP hydrolase GdpP in Bacillus subtilis

机译:σd依赖性的反义转录物调节枯草芽孢杆菌中环菌-i-amp水解酶Gdpp的表达

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Cyclic-di-AMP (c-di-AMP) is an essential second messenger in Bacillus subtilis, and depletion leads to defects in the integrity of the cell wall. Levels of c-di-AMP are regulated by both the rates of synthesis (by diadenylate cyclases) and the rates of degradation (by the GdpP phosphodiesterase, formerly YybT). Little is known about the regulation of gdpP expression or GdpP activity, but mutations that inactivate GdpP lead to high-level resistance to β-lactam antibiotics. Here we demonstrate that expression of gdpP is regulated by a cis-acting antisense RNA (gdpPas) in vivo. Transcription of this antisense RNA is initiated in the middle of the gdp gene and is dependent on an alternative sigma factor, σD, previously associated with the expression of late flagellar genes, chemotaxis proteins and cell wall autolytic enzymes. Changes in σD activity can modulate GdpP protein levels by ~2.5-fold, which may provide a mechanism for the cell to upregulate c-di-AMP levels in coordination with the activation of autolytic enzymes.
机译:环偶-AMP(C-DI-AMP)是枯草芽孢杆菌的必需第二信使,并且耗尽导致细胞壁完整性缺陷。 C-Di-AMP的水平通过合成率(通过二氧羰基环酶)和降解速度(通过GDPP磷酸二酯酶,以前的YYBT)来调节。关于调节GDPP表达或GDPP活性的难题少众所周知,但灭活GDPP的突变导致对β-内酰胺抗生素的高水平抗性。在这里,我们证明GDPP的表达由体内CIS作用反义RNA(GDPPA)调节。该反义RNA的转录在GDP基因的中间开始,依赖于先前与晚期鞭毛基因,趋化性蛋白质和细胞壁自化酶的表达相关的替代Σ因子。 σd活性的变化可以通过〜2.5倍调节GDPP蛋白水平,这可以提供细胞的机制,以使C-DI-AMP水平与自固溶性酶的激活相同。

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