Genomic Structure of the Cyanobacterium Synechocystis sp PCC 6803 Strain GT-S

被引:37
|
作者
Tajima, Naoyuki [1 ]
Sato, Shusei [2 ]
Maruyama, Fumito [3 ]
Kaneko, Takakazu [4 ]
Sasaki, Naobumi V. [1 ]
Kurokawa, Ken [5 ]
Ohta, Hiroyuki [6 ]
Kanesaki, Yu [7 ]
Yoshikawa, Hirofumi [7 ,8 ]
Tabata, Satoshi [2 ]
Ikeuchi, Masahiko [1 ]
Sato, Naoki [1 ]
机构
[1] Univ Tokyo, Grad Sch Arts & Sci, Dept Life Sci, Meguro Ku, Tokyo 1538902, Japan
[2] Kazusa DNA Res Inst, Kisarazu, Chiba 2920818, Japan
[3] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Sect Bacterial Pathogenesis, Bunkyo Ku, Tokyo 1138510, Japan
[4] Kyoto Sangyo Univ, Fac Life Sci, Kita Ku, Kyoto 6038555, Japan
[5] Tokyo Inst Technol, Dept Biol Informat, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[6] Tokyo Inst Technol, Ctr Biol Resources & Informat, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[7] Tokyo Univ Agr, Nodai Res Inst, Genome Res Ctr, Setagaya Ku, Tokyo 1568502, Japan
[8] Tokyo Univ Agr, Dept Biosci, Setagaya Ku, Tokyo 1568502, Japan
关键词
Synechocystis sp PCC 6803; genome re-sequencing; insertion sequence; single nucleotide polymorphism; CyanoClust; MULTIPLE SEQUENCE; SP PCC-6803; GENERATION; PROTEINS;
D O I
10.1093/dnares/dsr026
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Synechocystis sp. PCC 6803 is the most popular cyanobacterial strain, serving as a standard in the research fields of photosynthesis, stress response, metabolism and so on. A glucose-tolerant (GT) derivative of this strain was used for genome sequencing at Kazusa DNA Research Institute in 1996, which established a hallmark in the study of cyanobacteria. However, apparent differences in sequences deviating from the database have been noticed among different strain stocks. For this reason, we analysed the genomic sequence of another GT strain (GT-S) by 454 and partial Sanger sequencing. We found 22 putative single nucleotide polymorphisms (SNPs) in comparison to the published sequence of the Kazusa strain. However, Sanger sequencing of 36 direct PCR products of the Kazusa strains stored in small aliquots resulted in their identity with the GT-S sequence at 21 of the 22 sites, excluding the possibility of their being SNPs. In addition, we were able to combine five split open reading frames present in the database sequence, and to remove the C-terminus of an ORF. Aside from these, two of the Insertion Sequence elements were not present in the GT-S strain. We have thus become able to provide an accurate genomic sequence of Synechocystis sp. PCC 6803 for future studies on this important cyanobacterial strain.
引用
收藏
页码:393 / 399
页数:7
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