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首页> 外文期刊>Molecular Microbiology >Molecular characterization of long direct repeat (LDR) sequences expressing a stable mRNA encoding for a 35-amino-acid cell-killing peptide and a cis-encoded small antisense RNA in Escherichia coli.
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Molecular characterization of long direct repeat (LDR) sequences expressing a stable mRNA encoding for a 35-amino-acid cell-killing peptide and a cis-encoded small antisense RNA in Escherichia coli.

机译:在大肠杆菌中表达稳定的mRNA的长直接重复序列(LDR)的分子表征,该稳定的mRNA编码35个氨基酸的细胞杀伤肽和顺式编码的小反义RNA。

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摘要

Genome sequence analyses of Escherichia coli K-12 revealed four copies of long repetitive elements. These sequences are designated as long direct repeat (LDR) sequences. Three of the repeats (LDR-A, -B, -C), each approximately 500 bp in length, are located as tandem repeats at 27.4 min on the genetic map. Another copy (LDR-D), 450 bp in length and nearly identical to LDR-A, -B and -C, is located at 79.7 min, a position that is directly opposite the position of LDR-A, -B and -C. In this study, we demonstrate that LDR-D encodes a 35-amino-acid peptide, LdrD, the overexpression of which causes rapid cell killing and nucleoid condensation of the host cell. Northern blot and primer extension analysis showed constitutive transcription of a stable mRNA (approximately 370 nucleotides) encoding LdrD and an unstable cis-encoded antisense RNA (approximately 60 nucleotides), which functions as a trans-acting regulator of ldrD translation. We propose that LDR encodes a toxin-antitoxin module. LDR-homologous sequences are not pre-sent on any known plasmids but are conserved in Salmonella and other enterobacterial species.
机译:大肠杆菌K-12的基因组序列分析揭示了四个副本的长重复元素。这些序列称为长直接重复(LDR)序列。三个重复序列(LDR-A,-B,-C)的长度分别约为500 bp,在基因图谱上位于27.4分钟的串联重复序列中。另一个副本(LDR-D)的长度为450 bp,与LDR-A,-B和-C几乎相同,位于79.7分钟处,该位置与LDR-A,-B和-C的位置直接相对。在这项研究中,我们证明LDR-D编码一个35个氨基酸的肽LdrD,LdrD的过表达引起宿主细胞的快速细胞杀伤和核苷缩合。 Northern印迹和引物延伸分析表明,编码LdrD的稳定mRNA(约370个核苷酸)和不稳定的顺式反义RNA(约60个核苷酸)组成性转录,其作为ldrD翻译的反式调节因子。我们建议LDR编码毒素-抗毒素模块。 LDR同源序列在任何已知质粒中均不存在,但在沙门氏菌和其他肠细菌物种中是保守的。

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