Comparative analysis of the whole set of rRNA operons between an enterohemorrhagic Escherichia coli O157:H7 Sakai strain and an Escherichia coli K-12 strain MG1655

被引:14
作者
Ohnishi, M
Murata, T
Nakayama, K
Kuhara, S
Hattori, M
Kurokawa, K
Yasunaga, T
Yokoyama, K
Makino, K
Shinagawa, H
Hayashi, T
机构
[1] Shinshu Univ, Sch Med, Dept Bacteriol, Matsumoto, Nagano 3908621, Japan
[2] Kyushu Univ, Grad Sch Genet Resources Technol, Higashi Ku, Fukuoka 812, Japan
[3] Kitasato Univ, RIKEN, Genom Sci Ctr, Human Genome Res Grp, Sagamihara, Kanagawa 228, Japan
[4] Osaka Univ, Genome Informat Res Ctr, Suita, Osaka, Japan
[5] Osaka Univ, Microbial Dis Res Inst, Dept Mol Microbiol, Suita, Osaka, Japan
[6] Univ Tokyo, Human Genom Ctr, Inst Med Sci, Minato Ku, Tokyo, Japan
基金
日本学术振兴会;
关键词
rrn operon; direct sequencing; enterohemorrhagic E. coli O157 : H7; E. coli K-12; intraspecific variation; intercistronic variation;
D O I
10.1016/S0723-2020(00)80059-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Two primer sets for direct sequence determination of all seven rRNA operons (rrn)) of Escherichia coli have been developed; one is for specific-amplification of each nn operon and the other is for direct sequencing of the amplified operons. Using these primer sets, we determined the nucleotide sequences of seven rrn operons, including promoter and terminator regions, of an enterohemorrhagic E. coli (EHEC) O157:H7 Sakai strain. To elucidate the intercistronic or intraspecific variation of rin operons, their sequences were compared with those for the K-12 rrn operons. The rrn genes and the internal transcribed spacer regions showed a higher similarity to each other in each strain than between the corresponding operons of the two strains. However, the degree of intercistronic homogeneity was much higher in the EHEC strain than in K-12. In contrast, promoter and terminator regions in each operons were conserved between the corresponding operons of the two strains, which exceeded intercistronic similarity.
引用
收藏
页码:315 / 324
页数:10
相关论文
共 26 条
[1]  
Antón AI, 1999, J BACTERIOL, V181, P2703
[2]   Sequence diversity in the 16S-23S intergenic spacer region (ISR) of the rRNA operons in representatives of the Escherichia coli ECOR collection [J].
Antón, AI ;
Martínez-Murcia, AJ ;
Rodríguez-Valera, F .
JOURNAL OF MOLECULAR EVOLUTION, 1998, 47 (01) :62-72
[3]   The complete genome sequence of Escherichia coli K-12 [J].
Blattner, FR ;
Plunkett, G ;
Bloch, CA ;
Perna, NT ;
Burland, V ;
Riley, M ;
ColladoVides, J ;
Glasner, JD ;
Rode, CK ;
Mayhew, GF ;
Gregor, J ;
Davis, NW ;
Kirkpatrick, HA ;
Goeden, MA ;
Rose, DJ ;
Mau, B ;
Shao, Y .
SCIENCE, 1997, 277 (5331) :1453-+
[4]   GENE ORGANIZATION AND PRIMARY STRUCTURE OF A RIBOSOMAL-RNA OPERON FROM ESCHERICHIA-COLI [J].
BROSIUS, J ;
DULL, TJ ;
SLEETER, DD ;
NOLLER, HF .
JOURNAL OF MOLECULAR BIOLOGY, 1981, 148 (02) :107-127
[5]  
BROSIUS J, 1978, P NATL ACAD SCI USA, V75, P4801, DOI 10.1073/pnas.75.10.4801
[6]   NUCLEOTIDE SEQUENCE OF 5S-RIBOSOMAL RNA FROM ESCHERICHIA COLI [J].
BROWNLEE, GG ;
SANGER, F ;
BARRELL, BG .
NATURE, 1967, 215 (5102) :735-&
[7]   Sequence heterogeneities among 16S ribosomal RNA sequences, and their effect on phylogenetic analyses at the species level [J].
Cilia, V ;
Lafay, B ;
Christen, R .
MOLECULAR BIOLOGY AND EVOLUTION, 1996, 13 (03) :451-461
[8]   INTRASPECIFIC VARIATION IN SMALL-SUBUNIT RIBOSOMAL-RNA SEQUENCES IN GENBANK - WHY SINGLE SEQUENCES MAY NOT ADEQUATELY REPRESENT PROKARYOTIC TAXA [J].
CLAYTON, RA ;
SUTTON, G ;
HINKLE, PS ;
BULT, C ;
FIELDS, C .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1995, 45 (03) :595-599
[9]   COMPARISON OF THE EXPRESSION OF THE 7 RIBOSOMAL-RNA OPERONS IN ESCHERICHIA-COLI [J].
CONDON, C ;
PHILIPS, J ;
FU, ZY ;
SQUIRES, C ;
SQUIRES, CL .
EMBO JOURNAL, 1992, 11 (11) :4175-4185
[10]   IDENTIFICATION OF PROMOTER MUTANTS DEFECTIVE IN GROWTH-RATE-DEPENDENT REGULATION OF RIBOSOMAL-RNA TRANSCRIPTION IN ESCHERICHIA-COLI [J].
DICKSON, RR ;
GAAL, T ;
DEBOER, HA ;
DEHASETH, PL ;
GOURSE, RL .
JOURNAL OF BACTERIOLOGY, 1989, 171 (09) :4862-4870