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使用简并引物通过合成进行DNA测序。

DNA sequencing by synthesis with degenerate primers.

作者信息

Tang Chao, Shi Xiaolong, Li Xiujie, Lu Zuhong

机构信息

State Key Laboratory of Bioelectronics, Southeast University, Nanjing, China.

出版信息

J Genet Genomics. 2008 Sep;35(9):545-51. doi: 10.1016/S1673-8527(08)60074-0.

Abstract

The degenerate primer-based sequencing was developed by a synthesis method (DP-SBS) for high-throughput DNA sequencing, in which a set of degenerate primers are hybridized on the arrayed DNA templates and extended by DNA polymerase on microarrays. In this method, a different set of degenerate primers containing a given number (n) of degenerate nucleotides at the 3'-ends were annealed to the sequenced templates that were immobilized on the solid surface. The nucleotides (n+1) on the template sequences were determined by detecting the incorporation of fluorescent labeled nucleotides. The fluorescent labeled nucleotide was incorporated into the primer in a base-specific manner after the enzymatic primer extension reactions and nine-base length were read out accurately. The main advantage of the DP-SBS is that the method only uses very conventional biochemical reagents and avoids the complicated special chemical reagents for removing the labeled nucleotides and reactivating the primer for further extension. From the present study, it is found that the DP-SBS method is reliable, simple, and cost-effective for laboratory-sequencing a large amount of short DNA fragments.

摘要

基于简并引物的测序是通过一种合成方法(DP-SBS)开发的用于高通量DNA测序,其中一组简并引物与排列好的DNA模板杂交,并由DNA聚合酶在微阵列上进行延伸。在该方法中,一组在3'端含有给定数量(n)简并核苷酸的不同简并引物与固定在固体表面的测序模板退火。通过检测荧光标记核苷酸的掺入来确定模板序列上的核苷酸(n + 1)。在酶促引物延伸反应后,荧光标记核苷酸以碱基特异性方式掺入引物中,并准确读出九个碱基长度。DP-SBS的主要优点是该方法仅使用非常常规的生化试剂,避免了用于去除标记核苷酸和重新激活引物以进行进一步延伸的复杂特殊化学试剂。从本研究发现,DP-SBS方法对于在实验室中对大量短DNA片段进行测序是可靠、简单且具有成本效益的。

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