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A small, microRNA-size, ribonucleic acid regulating gene expression and development of Shiga toxin-converting bacteriophage Φ24Β

机译:一个微小的,微小RNA大小的核糖核酸,调控志贺毒素转化噬菌体Φ24Β的基因表达和发育

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A microRNA-size (20-nt long) molecule has been identified in Escherichia coli after induction of Shiga toxin-converting bacteriophage Φ24B. This small RNA, named 24B_1, is encoded in the lom - vb_24B_43 region of the phage genome, and apparently it is produced by cleavage of a larger transcript. A phage devoid of 24B_1 revealed decreased efficiency of lysogenization, quicker prophage induction after provoking the SOS response, higher efficiency of progeny phage production during the lytic cycle and less efficient adsorption on the host cells. Expression of most of phage genes was drastically increased after infection of E. coli by the Φ24BΔ24B_1 phage. Since 24B_1 may impair expression of the d_ant gene, coding for an anti-repressor, these results may explain the mechanism of regulations of the physiological processes by this small RNA due to impaired activity of the cI repressor and changed expression of vast majority of phage genes. To our knowledge, this is the first example of functional microRNA-size molecule in bacterial cells.
机译:在诱导志贺毒素转化噬菌体Φ24 B 后,在大肠杆菌中鉴定出一个微小RNA分子(长20nt)。这个名为24B_1的小RNA在噬菌体基因组的lom-vb_24B_43区域编码,并且显然是通过切割更大的转录物而产生的。缺乏24B_1的噬菌体显示出溶血原化的效率降低,激发SOS反应后诱导更快的噬菌体诱导,在裂解周期中产生子代噬菌体的​​效率更高,对宿主细胞的吸附效率更低。 Φ24 B Δ24B_1噬菌体感染大肠杆菌后,大多数噬菌体基因的表达急剧增加。由于24B_1可能会削弱编码抗阻遏物的d_ant基因的表达,因此这些结果可能解释了由于cI阻遏物活性受损和绝大多数噬菌体基因表达改变而导致的这种小RNA调节生理过程的机制。 。据我们所知,这是细菌细胞中功能性microRNA大小分子的第一个例子。

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