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在大肠杆菌中表达编码35个氨基酸的细胞杀伤肽的稳定信使核糖核酸(mRNA)和顺式编码的小反义核糖核酸(RNA)的长直接重复(LDR)序列的分子特征分析

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.

作者信息

Kawano Mitsuoki, Oshima Taku, Kasai Hiroaki, Mori Hirotada

机构信息

Research and Education Center for Genetic Information, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0101, Japan.

出版信息

Mol Microbiol. 2002 Jul;45(2):333-49. doi: 10.1046/j.1365-2958.2002.03042.x.

Abstract

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.

摘要

大肠杆菌K-12的基因组序列分析揭示了四个长重复元件拷贝。这些序列被指定为长直接重复(LDR)序列。其中三个重复序列(LDR-A、-B、-C),每个长度约为500 bp,在遗传图谱上位于27.4分钟处串联重复。另一个拷贝(LDR-D),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。在本研究中,我们证明LDR-D编码一种35个氨基酸的肽LdrD,其过表达会导致宿主细胞快速死亡和类核凝聚。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)和不稳定的顺式编码反义RNA(约60个核苷酸)组成型转录,反义RNA作为ldrD翻译的反式作用调节因子发挥作用。我们提出LDR编码一个毒素-抗毒素模块。LDR同源序列在任何已知质粒上均不存在,但在沙门氏菌和其他肠杆菌物种中保守。

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