Multiple group-specific sequencing primers for reliable and rapid DNA sequencing

被引:15
作者
Gharizadeh, B
Ohlin, A
Mölling, P
Bäckman, A
Amini, B
Olcén, P
Nyrén, P
机构
[1] Royal Inst Technol, Stockholm Ctr Phys Astron & Biotechnol, Dept Biotechnol, SE-10691 Stockholm, Sweden
[2] Orebro Univ Hosp, Dept Pediat, SE-70185 Orebro, Sweden
[3] Orebro Univ Hosp, Dept Clin Microbiol, SE-70185 Orebro, Sweden
关键词
group-specific multiple sequencing primers; DNA sequencing; non-specific amplification products; Pyrosequencing technology;
D O I
10.1016/S0890-8508(03)00054-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Pyrosequencing(TM) technology is a bioluminometric DNA sequencing method that employs a cascade of four enzymes to deliver sequence signals. To date this technology has been limited to the sequencing of short stretches of DNA. As an improvement to this technique, we have introduced a bacterial group-specific, multiple sequencing primer approach that circumvents sequencing of less informative semi-conservative regions of the 16S rRNA gene. This new approach is suitable for challenging templates, improving sequence data quality, avoiding sequencing of non-specific amplification products, lessening sequencing time, and moreover, this strategy should open the way for many new applications in the future. The group-specific, multiple sequencing primers can be applied in the Sanger dideoxy sequencing method as well. In addition, we have improved the chemistry of the Pyrosequencing system enabling sequencing of longer stretches of DNA, which allows numerous new applications. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:203 / 210
页数:8
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