Kawano Mitsuoki, Oshima Taku, Kasai Hiroaki, Mori Hirotada
Research and Education Center for Genetic Information, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0101, Japan.
Mol Microbiol. 2002 Jul;45(2):333-49. doi: 10.1046/j.1365-2958.2002.03042.x.
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.
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。