Sekiua T, Ormondt H V, Khorana H G
J Biol Chem. 1975 Feb 10;250(3):1087-98.
The sequence of 29 nucleotides in the region preceding the initiation of the transcription of the Escherichia coli tyrosine tRNA gene has been determined. This is: (5') ---GGGGCGCATCATATCAAATGACGCGCCGC--- (3') (3') ---CCCCGCGTAGTATAGTTTACTGCGGCGGCG--- (5'). The general approach used for the sequence determination involved the DNA polymerase I-catalyzed elongation of suitable deoxyribopolynucleotide primers when hybridized to the 1-strand of phi80psuIII plus DNA at the appropriate site. Sequences of the newly grown oligonucleotide chains were determined by a combination of two-dimensional fingerprinting following partial exonucleolytic degradation, nearst neighbor analyses, and determination of pyrimidine tracts. Primer elongations were carried out in a controlled and stepwise manner and the newly grown oligonucleotide chains were kept short by incorporating the following features into the method: (a) the insertion of a ribonucleotide unit at or near the 3' terminus of the primers; (b) the use of a maximum of three nucleoside 5'-triphosphates in the first stage of the elongation reaction isolation of the elongated primer, and its reuse in a second step together with different sets of deoxy-nucleoside triphosphates; and (c) elongation of the primer using all of the four nucleoside triphosphates with one of the triphosphates being supplied in a limiting concentration.
已确定大肠杆菌酪氨酸tRNA基因转录起始前区域的29个核苷酸序列。其序列如下:(5')---GGGGCGCATCATATCAAATGACGCGCCGC---(3')(3')---CCCCGCGTAGTATAGTTTACTGCGGCGGCG---(5')。用于序列测定的一般方法包括:当合适的脱氧核糖多核苷酸引物与phi80psuIII加DNA的1链在适当位点杂交时,由DNA聚合酶I催化其延伸。新合成的寡核苷酸链的序列通过以下方法组合确定:部分核酸外切降解后的二维指纹图谱、最近邻分析以及嘧啶序列的测定。引物延伸以可控且逐步的方式进行,并且通过将以下特征纳入该方法使新合成的寡核苷酸链保持较短:(a)在引物的3'末端或其附近插入一个核糖核苷酸单元;(b)在延伸反应的第一阶段使用最多三种核苷5'-三磷酸,分离延伸后的引物,并在第二步中与不同组的脱氧核苷三磷酸一起重复使用;(c)使用所有四种核苷三磷酸延伸引物,其中一种三磷酸以限制浓度提供。