Shibata Kazuhiro, Izawa Masaki, Hayashizaki Yoshihide, Watahiki Masanori
Genome Science Laboratory, RIKEN Discovery and Research Institute, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
J Struct Funct Genomics. 2003;4(1):35-9. doi: 10.1023/a:1024677331154.
Transcriptional sequencing (TS) is a method that differs considerably from conventional sequencing methods. These differences include the use RNA polymerases with rNTPs and 3'-dNTPs as substrates and terminators respectively, and initiation from double stranded promoters on templates of ds-DNA. We used TS in an attempt to sequence 33 clones whose electropherogram peaks suddenly became absent or weak with conventional sequencing methods. All of the TS reactions overcame the difficulty in sequencing the problematic target regions of the 33 clones. Therefore, TS can be applied to sequence not only GC-rich regions, but also whole genome sequences with a high GC content.
转录测序(TS)是一种与传统测序方法有很大差异的方法。这些差异包括分别使用以核糖核苷三磷酸(rNTPs)和3'-脱氧核苷三磷酸(3'-dNTPs)作为底物和终止剂的RNA聚合酶,以及从双链DNA(ds-DNA)模板上的双链启动子起始。我们使用TS试图对33个克隆进行测序,这些克隆的电泳图峰在传统测序方法中突然消失或变弱。所有的TS反应都克服了对这33个克隆的有问题靶区域进行测序的困难。因此,TS不仅可以应用于富含GC区域的测序,还可以应用于高GC含量的全基因组序列测序。