Stoflet E S, Koeberl D D, Sarkar G, Sommer S S
Department of Biochemistry and Molecular Biology, Mayo Clinic/Foundation, Rochester, MN 55905.
Science. 1988 Jan 29;239(4839):491-4. doi: 10.1126/science.3340835.
A sequencing method called genomic amplification with transcript sequencing (GAWTS) is described that is based on amplification with the polymerase chain reaction (PCR). GAWTS bypasses cloning and increases the rate of sequence acquisition by at least fivefold. The method involves the attachment of a phage promoter onto at least one of the PCR primers. The segments amplified by PCR are transcribed to further increase the signal and to provide an abundance of single-stranded template for reverse transcriptase-mediated dideoxy sequencing. An end-labeled reverse transcriptase primer complementary to the desired sequence generates the additional specificity required to generate unambiguous sequence data. GAWTS can be performed on as little as a nanogram of genomic DNA. The rate of GAWTS can be increased by coamplification and cotranscription of multiple regions as illustrated by two regions of the factor IX gene. Since GAWTS lends itself well to automation, further increases in the rate of sequence acquisition can be expected.
描述了一种称为转录测序基因组扩增(GAWTS)的测序方法,该方法基于聚合酶链反应(PCR)扩增。GAWTS绕过克隆,将序列获取率提高至少五倍。该方法包括将噬菌体启动子连接到至少一个PCR引物上。通过PCR扩增的片段被转录以进一步增加信号,并为逆转录酶介导的双脱氧测序提供大量单链模板。与所需序列互补的末端标记逆转录酶引物产生生成明确序列数据所需的额外特异性。GAWTS可以在低至一纳克的基因组DNA上进行。如因子IX基因的两个区域所示,通过多个区域的共扩增和共转录可以提高GAWTS的速率。由于GAWTS非常适合自动化,预计序列获取率会进一步提高。