Highly accurate genome sequences of Escherichia coli K-12 strains MG1655 and W3110

被引:378
作者
Hayashi, Koji
Morooka, Naoki
Yamamoto, Yoshihiro
Fujita, Katsutoshi
Isono, Katsumi
Choi, Sunju
Ohtsubo, Eiichi
Baba, Tomoya
Wanner, Barry L.
Mori, Hirotada
Horiuchi, Takashi
机构
[1] Natl Inst Basic Biol, Div Genome Dynam, Okazaki, Aichi 4448585, Japan
[2] Purdue Univ, Dept Biol Sci, W Lafayette, IN 47907 USA
[3] Hyogo Coll Med, Nishinomiya, Hyogo, Japan
[4] Kobe Univ, Grad Sch Sci & Technol, Kobe, Hyogo 657, Japan
[5] Univ Tokyo, Inst Mol & Cell Biosci, Bunkyo Ku, Tokyo, Japan
[6] Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata, Japan
[7] Nara Inst Sci & Technol, Ikoma, Nara, Japan
关键词
crp mutation; E. coli K-12 genome; E. coli K-12 pedigree; genome corrections; rpoS mutations;
D O I
10.1038/msb4100049
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
With the goal of solving the whole-cell problem with Escherichia coli K-12 as a model cell, highly accurate genomes were determined for two closely related K-12 strains, MG1655 and W3110. Completion of the W3110 genome and comparison with the MG1655 genome revealed differences at 267 sites, including 251 sites with short, mostly single-nucleotide, insertions or deletions (indels) or base substitutions (totaling 358 nucleotides), in addition to 13 sites with an insertion sequence element or defective prophage in only one strain and two sites for the W3110 inversion. Direct DNA sequencing of PCR products for the 251 regions with short indel and base disparities revealed that only eight sites are true differences. The other 243 discrepancies were due to errors in the original MG1655 sequence, including 79 frameshifts, one amino-acid residue deletion, five amino-acid residue insertions, 73 missense, and 17 silent changes within coding regions. Errors in the original MG1655 sequence (< 1 per 13000 bases) were mostly within portions sequenced with out-dated technology based on radioactive chemistry.
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页数:5
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