Khrapko K R, Khorlyn A A, Shick V V, Florentiev V L, Mirzabekov A D
V.A. Engelhardt Institute of Molecular Biology, Academy of Sciences of the USSR, Moscow.
FEBS Lett. 1989 Oct 9;256(1-2):118-22. doi: 10.1016/0014-5793(89)81730-2.
We have proposed a DNA sequencing method based on hybridization of a DNA fragment to be sequenced with the complete set of fixed-length oligonucleotides (e.g., 4(8) = 65,536 possible 8-mers) immobilized individually as dots of a 2-D matrix [(1989) Dokl. Akad. Nauk SSSR 303, 1508-1511]. It was shown that the list of hybridizing octanucleotides is sufficient for the computer-assisted reconstruction of the structures for 80% of random-sequence fragments up to 200 bases long, based on the analysis of the octanucleotide overlapping. Here a refinement of the method and some experimental data are presented. We have performed hybridizations with oligonucleotides immobilized on a glass plate, and obtained their dissociation curves down to heptanucleotides. Other approaches, e.g., an additional hybridization of short oligonucleotides which continuously extend duplexes formed between the fragment and immobilized oligonucleotides, should considerably increase either the probability of unambiguous reconstruction, or the length of reconstructed sequences, or decrease the size of immobilized oligonucleotides.
我们提出了一种DNA测序方法,该方法基于待测序的DNA片段与固定在二维矩阵中的完整固定长度寡核苷酸集(例如,4⁸ = 65536种可能的8聚体)杂交[(1989) Dokl. Akad. Nauk SSSR 303, 1508 - 1511]。结果表明,基于八核苷酸重叠分析,杂交八核苷酸列表足以对80%长度达200个碱基的随机序列片段进行计算机辅助结构重建。本文给出了该方法的改进及一些实验数据。我们用固定在玻璃板上的寡核苷酸进行了杂交,并获得了直至七核苷酸的解离曲线。其他方法,例如短寡核苷酸的额外杂交,这种杂交可连续延长片段与固定寡核苷酸之间形成的双链,应能显著提高明确重建的概率,或增加重建序列的长度,或减小固定寡核苷酸的大小。