Yamada Y, Ohki M, Ishikura H
Nucleic Acids Res. 1983 May 25;11(10):3037-45. doi: 10.1093/nar/11.10.3037.
Clones carring Bacillus subtilis tRNA genes were isolated from a lambda 816 library. A recombinant phage lambda 816-BS83 which was hybridized effectively with unfractionated tRNA probes contained a 3-kb fragment. By a Southern's blot analysis, it was found that tRNA genes were located in Eco RI-Hinc II region of this fragment. Sequence determination revealed the presence of a cluster of four tRNA genes in this region. The gene organization was as follows: tDNALys-9bp-tDNAGlu-81bp-tDNAAsp-30bp-tDNAPhe. The RNA sequences expected from tDNALys and tDNAPhe were identical with the reported RNA sequences. Two tRNA genes, tDNALys and tDNAAsp encoded the CCA sequence of 3'-terminal region, but the other two, tDNAGlu and tDNAPhe did not. A promoter-like sequence which corresponds to the sigma 55-recognition site was found in a region about 100bp upstream from tDNALys.
从λ816文库中分离出携带枯草芽孢杆菌tRNA基因的克隆。一个与未分级的tRNA探针有效杂交的重组噬菌体λ816 - BS83含有一个3kb的片段。通过Southern印迹分析发现,tRNA基因位于该片段的Eco RI - Hinc II区域。序列测定表明该区域存在四个tRNA基因簇。基因组织如下:tDNALys - 9bp - tDNAGlu - 81bp - tDNAAsp - 30bp - tDNAPhe。tDNALys和tDNAPhe预期的RNA序列与报道的RNA序列相同。两个tRNA基因tDNALys和tDNAAsp编码3'末端区域的CCA序列,但另外两个tDNAGlu和tDNAPhe不编码。在tDNALys上游约100bp的区域发现了一个与σ55识别位点相对应的启动子样序列。