Biology Department, Brandeis University, 415 South St., Waltham, MA 02155, USA.
Nucleic Acids Res. 2010 Jun;38(11):e119. doi: 10.1093/nar/gkq111. Epub 2010 Feb 26.
We have recently described a Dilute-'N'-Go protocol that greatly simplifies preparation and sequencing of both strands of an amplicon generated using linear-after-the-exponential (LATE)-PCR, an advanced form of asymmetric PCR . The same protocol can also be used to sequence all limiting primer strands in a multiplex LATE-PCR, by adding back each of the depleted limiting primers to a separate aliquot of the multiplex reaction. But, Dilute-'N'-Go sequencing cannot be used directly to sequence each of the excess primer strands in the same multiplex reaction, because all of the excess primers are still present at high concentration. This report demonstrates for the first time that it is possible to sequence each of the excess primer strands using a modified Dilute-'N'-Go protocol in which blockers are added to prevent all but one of the excess primers serving as the sequencing primer in separate aliquots. The optimal melting temperatures, positions and concentrations of blockers relative to their corresponding excess primers are defined in detail. We are using these technologies to measure DNA sequence changes in mitochondrial genomes that accompany aging and exposure to certain drugs.
我们最近描述了一种 Dilute-'N'-Go 方案,该方案极大地简化了使用线性后指数(LATE)-PCR 产生的扩增子的两条链的制备和测序,LATE-PCR 是一种先进的不对称 PCR 形式。同一方案也可用于通过将每种耗尽的限制引物添加回多重 LATE-PCR 的单独等分试样中,来对多重 LATE-PCR 中的所有限制引物链进行测序。但是,Dilute-'N'-Go 测序不能直接用于对同一多重反应中的每个过量引物链进行测序,因为所有过量的引物仍处于高浓度。本报告首次证明,通过添加阻滞剂来防止过量引物中的除一条以外的所有引物在单独的等分试样中用作测序引物,使用改良的 Dilute-'N'-Go 方案可以对每个过量引物链进行测序。详细定义了相对于其相应的过量引物的阻滞剂的最佳熔解温度、位置和浓度。我们正在使用这些技术来测量伴随衰老和暴露于某些药物的线粒体基因组中的 DNA 序列变化。