Guanine-rich sequences inhibit proofreading DNA polymerases

被引:9
|
作者
Zhu, Xiao-Jing [1 ]
Sun, Shuhui [1 ]
Xie, Binghua [1 ]
Hu, Xuemei [2 ]
Zhang, Zunyi [1 ]
Qiu, Mengsheng [1 ,2 ]
Dai, Zhong-Min [1 ]
机构
[1] Hangzhou Normal Univ, Coll Life Sci, Key Lab Organ Dev & Regenerat Zhejiang Prov, Inst Life Sci, Hangzhou 310036, Zhejiang, Peoples R China
[2] Univ Louisville, Dept Anat Sci & Neurobiol, Louisville, KY 40292 USA
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
中国国家自然科学基金;
关键词
ENZYMATIC AMPLIFICATION;
D O I
10.1038/srep28769
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
DNA polymerases with proofreading activity are important for accurate amplification of target DNA. Despite numerous efforts have been made to improve the proofreading DNA polymerases, they are more susceptible to be failed in PCR than non-proofreading DNA polymerases. Here we showed that proofreading DNA polymerases can be inhibited by certain primers. Further analysis showed that G-rich sequences such as GGGGG and GGGGHGG can cause PCR failure using proofreading DNA polymerases but not Taq DNA polymerase. The inhibitory effect of these G-rich sequences is caused by G-quadruplex and is dose dependent. G-rich inhibitory sequence-containing primers can be used in PCR at a lower concentration to amplify its target DNA fragment.
引用
收藏
页数:8
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