Bossi L
Mol Gen Genet. 1983;192(1-2):163-70. doi: 10.1007/BF00327662.
In S. typhimurium, the hisR locus is defined by mutations causing reduced levels of the histidine transfer RNA. As a preliminary step in the analysis of the hisR mutants, a 972 bp DNA fragment containing the histidine tRNA gene from wild-type Salmonella was cloned and completely sequenced. This analysis revealed the existence of a tRNA gene cluster which, in addition to the tRNAHis gene, includes the genes for tRNALeu1, tRNAPro1 and a tentative tRNAArgCGG. All four tRNA genes are present as single copies and are separated by spacer sequences ranging from 20 to 53 bp in length. The gene cluster is efficiently transcribed in vitro by E. coli RNA polymerase and yields a transcript, approximately 480 nucleotides long, which contains all four tRNA sequences. This tetrameric precursor can be processed to 4S RNA in vitro with a wild-type Salmonella extract, but not with an extract prepared from a hisU (RNase P) mutant. Using portions of the tRNA gene cluster as specific hybridization probes, various processing intermediates were shown to accumulate in vivo in the hisU mutant. Most of these RNAs are monomeric precursors only a few nucleotides longer than the respective mature tRNA species.
在鼠伤寒沙门氏菌中,hisR位点由导致组氨酸转移RNA水平降低的突变所定义。作为分析hisR突变体的初步步骤,克隆了一个包含野生型沙门氏菌组氨酸tRNA基因的972 bp DNA片段并进行了全序列测定。该分析揭示了一个tRNA基因簇的存在,除了tRNAHis基因外,还包括tRNALeu1、tRNAPro1基因以及一个推测的tRNAArgCGG基因。所有四个tRNA基因均以单拷贝形式存在,由长度在20至53 bp之间的间隔序列隔开。该基因簇在体外可被大肠杆菌RNA聚合酶有效转录,并产生一个约480个核苷酸长的转录本,其中包含所有四个tRNA序列。这种四聚体前体在体外能用野生型沙门氏菌提取物加工成4S RNA,但不能用从hisU(核糖核酸酶P)突变体制备的提取物加工。使用tRNA基因簇的部分作为特异性杂交探针,结果表明各种加工中间体在hisU突变体的体内积累。这些RNA中的大多数是单体前体,仅比各自的成熟tRNA种类长几个核苷酸。