Sekiya T, Gait M J, Noris K, Ramamoorthy B, Khorana H G
J Biol Chem. 1976 Aug 10;251(15):4481-9.
The sequence of the first 29 nucleotides in the promoter region of a tyrosine tRNA gene has previously been determined (Sekiya, T., van Ormondt, H., and Khorana, H.G. (1975) J. Biol. Chem. 250, 1087-1098). This work has now been extended to give the sequence of a total of 59 nucleotides; the sequence is as follows: (see article). The general approach used in the determination of the sequence involved the DNA polymerase I-catalyzed elongation of synthetic deoxyribopolynucleotide primers hydridized to the l-strand of phi80psu+III DNA at the appropriate site. Sequencing of the newly added nucleotides was facilitated by the use of a number of techniques including (a) elongation of the primer with the use of all of the four nucleoside 5'-triphosphates but limiting the concentration of one of the triphosphates, (b) insertion of ribonucleotide units at appropriate sites so as to permit subsequent specific cleavages by pancreatic RNase, and (c) two-dimensional fingerprinting of the oligonucleotides in conjunction with partial exonucleolytic degradation, comprehensive nearest neighbor analyses, and the determination of pyrimidine tracts.
先前已确定了酪氨酸tRNA基因启动子区域前29个核苷酸的序列(关谷敏郎、范·奥蒙德特、霍拉纳(1975年)《生物化学杂志》250卷,1087 - 1098页)。现在这项工作已扩展至总共59个核苷酸的序列测定;序列如下:(见文章)。测定该序列所采用的总体方法涉及在适当位点,DNA聚合酶I催化与phi80psu + III DNA的l链杂交的合成脱氧核糖多核苷酸引物的延伸。通过使用多种技术有助于对新添加核苷酸进行测序,这些技术包括:(a)使用所有四种核苷5'-三磷酸但限制其中一种三磷酸的浓度来延伸引物;(b)在适当位点插入核糖核苷酸单元,以便随后通过胰核糖核酸酶进行特异性切割;以及(c)对寡核苷酸进行二维指纹图谱分析,并结合部分核酸外切降解、全面的相邻碱基分析以及嘧啶序列的测定。