Desai S M, Hunt C, Locker J, Weiss S B
J Biol Chem. 1978 Sep 25;253(18):6544-50.
The tRNA genes of bacteriophage T5 are located in four clusters on the continuous heavy DNA strand (Chen, M.-J., Locker, J., and Weiss, S.B. (1976) J. Biol. Chem. 251, 536--547). Three of the four clusters are within the DNA C segment; the fourth cluster, to which only tRNAArg has been localized, maps in a 3.02 kilobase (kb) region of which 1.99 kb are at the right end of the C segment and 1.03 kb at the left end of the D segment. In order to localize the tRNAArg gene further and to define its relationship to the C-D nick, we devised a suitable method for preparing T5 DNA fragments whose ends correspond to the position of the T5 DNA nicks contained in the light DNA strand. In this method, DNA is denatured, partially renatured, and digested with low concentrations of S1 nuclease. Agarose-gel electrophoresis of these digests gives a pattern of bands which correlate in size with the pattern expected from the nicked structure of T5 DNA. Annealing of individual purified T5 [35P]tRNA species to the T5 DNA fragments transferred to nitrocellulose filters shows that tRNAArg hybridizes exclusively to the D fragment and is therefore localized to 1.03 kb at the 5' (left) end of the heavy strand of the D segment. This finding suggests that the promotor for this early gene is to the right of the C-D nick in T5 DNA; hence, the C-D nick does not coincide with this early promotor.
噬菌体T5的tRNA基因位于连续的重DNA链上的四个簇中(Chen,M.-J.,Locker,J.和Weiss,S.B.(1976年)《生物化学杂志》251,536 - 547)。四个簇中的三个位于DNA C片段内;第四个簇,仅tRNAArg已定位于此,位于一个3.02千碱基(kb)的区域,其中1.99 kb在C片段的右端,1.03 kb在D片段的左端。为了进一步定位tRNAArg基因并确定其与C - D切口的关系,我们设计了一种合适的方法来制备T5 DNA片段,其末端对应于轻DNA链中所含T5 DNA切口的位置。在这种方法中,DNA被变性、部分复性,并用低浓度的S1核酸酶消化。这些消化产物的琼脂糖凝胶电泳给出了一组条带模式,其大小与T5 DNA切口结构预期的模式相关。将单个纯化的T5 [35P]tRNA种类与转移到硝酸纤维素滤膜上的T5 DNA片段退火,结果表明tRNAArg仅与D片段杂交,因此定位于D片段重链5'(左)端的1.03 kb处。这一发现表明,这个早期基因的启动子在T5 DNA中C - D切口的右侧;因此,C - D切口与这个早期启动子不一致。