Fan J, Ranu R S, Smith C, Ruan C, Fuller C W
Colorado State University, Fort Collins, USA.
Biotechniques. 1996 Dec;21(6):1132-7. doi: 10.2144/96216pf01.
A new approach to DNA sequencing is described. The method is based on the use of [alpha-33P]-labeled dideoxyribonucleoside triphosphate terminators and Thermo Sequenase DNA polymerase in cycle sequencing. Thermo Sequenase DNA polymerase incorporates ddNTPs as efficiently as dNTPs, allowing the use of low concentrations of these nucleotides in DNA sequencing. Because only the properly terminated chains are labeled and visualized on autoradiography of the sequencing gels, the sequence results are free of background. The intensity of DNA bands generated are remarkably uniform, which makes reading of DNA sequences easy. By staggered loading of the sequencing gel (at 2-3 hour intervals), it is possible to sequence DNA at least 450 to 500 nucleotides. Exposure time for autoradiography with [alpha-33P] labels is much shorter than with [35S] and does not substantially compromise autoradiographic resolution. Data can be obtained after only 12 hours of exposure of an X-ray film. Moreover, cycle sequencing requires very small amounts of single- or double-stranded template. Consequently, it is even possible to generate sequence data from a single bacterial colony. The details of the protocol are presented in a stepwise manner, and some important parameters to be considered for sequencing with this method are discussed.
本文描述了一种DNA测序的新方法。该方法基于在循环测序中使用[α-33P]标记的双脱氧核糖核苷三磷酸终止剂和热稳定DNA聚合酶。热稳定DNA聚合酶掺入双脱氧核苷酸三磷酸(ddNTPs)的效率与掺入脱氧核苷酸三磷酸(dNTPs)的效率相同,这使得在DNA测序中可以使用低浓度的这些核苷酸。由于在测序凝胶的放射自显影片上只有正确终止的链被标记并可视化,所以序列结果没有背景干扰。所产生的DNA条带强度非常均匀,这使得读取DNA序列变得容易。通过在测序凝胶上交错加样(间隔2 - 3小时),可以对至少450至500个核苷酸的DNA进行测序。用[α-33P]标记进行放射自显影的曝光时间比用[35S]标记短得多,并且不会显著影响放射自显影分辨率。仅对X射线胶片曝光12小时后就能获得数据。此外,循环测序所需的单链或双链模板量非常少。因此,甚至有可能从单个细菌菌落生成序列数据。本文逐步介绍了该方案的细节,并讨论了使用此方法进行测序时需要考虑的一些重要参数。