Kleid D G, Agarwal K L, Khorana H G
J Biol Chem. 1975 Jul 25;250(14):5574-82.
The sequence of 18 nucleotides in the region preceding the initiation of transcription of the gene N of bacteriophage lambda has been determined to be as follows (see article). The basic approach used for the sequence determination involved Escherichia coli DNA polymerase I-catalyzed elongation of the octadecanucleotide primer, dT-C-A-G-T-G-C-G-T-C-C-T-G-C-T-G-A-rU, possessing the appropriate polarity and nucleotide sequence corresponding to the 5' end of the gene N transcript. Following hybridization of the primer to the r-stand of bacteriophage lambda CI85657, sequences of the newly grown ollgonucleotide chains were determined by a) partial exonuclease digestion followed by two-dimensional fingerprinting; b) determination of pyrimidine tracts; and c) nearest neighbor analyses. Primer elongation was carried out in a controlled manner, the size of the newly grown chains being kept short by the following techniques: a) insertion of a ribonucleotide unit as the 3' terminus of the primer; b) use of a limited number of deoxynucleoside 5'-triphosphates in the elongation reaction; and c) enlongation of the primer using all the four nucleoside triphosphates with one of the triphosphates being supplied in a limiting concentration.
噬菌体λ基因N转录起始前区域的18个核苷酸序列已确定如下(见文章)。用于序列测定的基本方法包括利用大肠杆菌DNA聚合酶I催化具有适当极性和与基因N转录本5'端相对应核苷酸序列的十八聚体引物dT-C-A-G-T-G-C-G-T-C-C-T-G-C-T-G-A-rU进行延伸。在引物与噬菌体λCI85657的r链杂交后,通过以下方法确定新合成的寡核苷酸链的序列:a)部分核酸外切酶消化后进行二维指纹图谱分析;b)嘧啶序列测定;c)相邻碱基分析。引物延伸以可控方式进行,通过以下技术使新合成链的长度保持较短:a)在引物的3'末端插入一个核糖核苷酸单元;b)在延伸反应中使用有限数量的脱氧核苷5'-三磷酸;c)使用所有四种核苷三磷酸进行引物延伸,其中一种三磷酸以限制浓度提供。