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

被引:116
作者
Kawano, M
Oshima, T
Kasai, H
Mori, H
机构
[1] Nara Inst Sci & Technol, Res & Educ Ctr Genet Informat, Nara 6300101, Japan
[2] Marine Biotechnol Inst, Kamaishi Labs, Iwate 0260001, Japan
关键词
D O I
10.1046/j.1365-2958.2002.03042.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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 (approximate to 370 nucleotides) encoding LdrD and an unstable cis -encoded antisense RNA (approximate to 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 present on any known plasmids but are conserved in Salmonella and other enterobacterial species.
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页码:333 / 349
页数:17
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