Maruyama Tatsuo, Shinohara Toshimitsu, Hosogi Takuya, Ichinose Hirofumi, Kamiya Noriho, Goto Masahiro
Department of Applied Chemistry, Graduate School of Engineering and Center for Future Chemistry, Kyushu University, Fukuoka 812-8581, Japan.
Anal Biochem. 2006 Jul 1;354(1):8-14. doi: 10.1016/j.ab.2006.03.056. Epub 2006 May 2.
Guanine quenching of a fluorescence-labeled DNA probe is a powerful tool for detecting a mutation in a targeted site of a DNA strand. However, a different guanine adjacent to a targeted site can interfere with detection of a point mutation, resulting in unsatisfactory sensitivity. In the current study, we developed a simple method to improve sensitivity of the guanine quenching method using a masking DNA oligonucleotide. The simple addition of a masking DNA oligonucleotide was found to mask the interference of a different guanine in a target oligonucleotide on fluorescence and to enhance difference in the quenching ratio between wild-type and mutant oligonucleotides. Based on this strategy, we succeeded in discriminating various mutations from the wild-type YMDD motif of the hepatitis B virus DNA polymerase gene using guanine quenching with a masking oligonucleotide.
荧光标记的DNA探针的鸟嘌呤淬灭是检测DNA链靶向位点突变的有力工具。然而,靶向位点附近的不同鸟嘌呤会干扰点突变的检测,导致灵敏度不尽人意。在本研究中,我们开发了一种简单的方法,通过使用掩蔽DNA寡核苷酸来提高鸟嘌呤淬灭法的灵敏度。发现简单地添加掩蔽DNA寡核苷酸可掩盖靶寡核苷酸中不同鸟嘌呤对荧光的干扰,并增强野生型和突变型寡核苷酸之间淬灭率的差异。基于此策略,我们成功地利用掩蔽寡核苷酸的鸟嘌呤淬灭从乙型肝炎病毒DNA聚合酶基因的野生型YMDD基序中鉴别出各种突变。