Chiaruttini C, Milet M
Institut de Biologie Physico-chimique, Paris, France.
J Mol Biol. 1993 Mar 5;230(1):57-76. doi: 10.1006/jmbi.1993.1126.
Southern blot analysis of genomic DNA of the mesophilic lactic bacterium Lactococcus lactis subsp. lactis strain IL1403, illuminated six rRNA gene clusters. Each cluster contains one copy each of three rRNA genes, displaying the typical eubacterial organization of physically linked 16 S, 23 S and 5 S rRNA genes. Five of the six rRNA clusters were cloned into plasmid pBR322. One recombinant plasmid, pSLCM6, containing a 6500 base-pair genomic DNA fragment, was characterized by physical mapping and the sequences encoding rRNAs and tRNAs were localized by Southern hybridization. This fragment contains a single operon composed of one promoter, a leader sequence, a 16 S rRNA gene, a tRNA(Ala) gene, a 23 S rRNA gene, a 5 S rRNA gene and a tRNA(Asn) gene. S1 nuclease mapping and primer extension analysis of in vivo transcripts localized one transcriptional initiation site 150 base-pairs upstream from the start of the 16 S rRNA gene. These procedures also suggest that this transcript is processed by an RNAse III-like activity similar to Bacillus subtilis; i.e. the L. lactis nuclease might be sequence-specific. The chronology of specific cleavages occurring during the maturation process of the precursor transcript is described. One interesting observation is that the regions flanking the 16 S and 23 S rRNAs containing the primary processing sites are identical and contain sequences that could be involved in transcriptional antitermination. S1 mapping of the 3' ends of in vivo transcripts indicate that a terminator-like sequence a few base-pairs downstream from the distal tRNA(Asn) gene is inefficient in arresting transcription.
对嗜温乳酸菌乳酸乳球菌乳酸亚种IL1403的基因组DNA进行Southern杂交分析,发现了6个rRNA基因簇。每个基因簇包含三个rRNA基因的各一个拷贝,呈现出典型的真细菌中物理连接的16S、23S和5S rRNA基因的组织形式。6个rRNA基因簇中的5个被克隆到质粒pBR322中。通过物理图谱分析对一个含有6500个碱基对基因组DNA片段的重组质粒pSLCM6进行了表征,并通过Southern杂交确定了编码rRNA和tRNA的序列的位置。该片段包含一个单一操纵子,由一个启动子、一个前导序列、一个16S rRNA基因、一个tRNA(Ala)基因、一个23S rRNA基因、一个5S rRNA基因和一个tRNA(Asn)基因组成。对体内转录本进行S1核酸酶图谱分析和引物延伸分析,确定了一个转录起始位点位于16S rRNA基因起始位点上游150个碱基对处。这些实验还表明,该转录本是由一种类似于枯草芽孢杆菌的RNase III样活性进行加工的;即乳酸乳球菌核酸酶可能具有序列特异性。描述了前体转录本成熟过程中发生的特异性切割的时间顺序。一个有趣的发现是,16S和23S rRNA侧翼含有主要加工位点的区域是相同的,并且包含可能参与转录抗终止的序列。对体内转录本3'末端的S1图谱分析表明,在远端tRNA(Asn)基因下游几个碱基对处的一个类似终止子的序列在阻止转录方面效率不高。