Rasmussen O F, Christiansen C
Genetic Engineering Group, Technical University of Denmark, Lyngby, Denmark.
Isr J Med Sci. 1987 May;23(5):342-6.
Four clones harboring fragments of the rRNA cistrons have been isolated from a genomic library of Mycoplasma PG50 DNA. By heteroduplex and displacement loop analysis, supplemented with sequence data, we demonstrate that the four clones together cover the two rRNA cistrons of Mycoplasma PG50 as well as the flanking regions. Parts of the cloned fragments have been analyzed in detail, and the following conclusions have been reached. Genes for tRNALys and tRNALeu are located about 450 bp upstream of the 16S rRNA gene of rrnA. An open reading frame of at least 215 codons is located just upstream of and in the same direction as rrnB. Analysis of the 3' flanking region of rrnA reveals that no tRNA genes succeed this operon. Also here an open reading frame can be identified, which is at least 83 codons long and has a putative promoter and a possible ribosome binding site. Its direction is the same as that of rrnA. None of the open reading frames has any function assigned yet. The last 880 bp of the 23S and the 5S genes of rrnA are compared with the corresponding Bacillus subtilis sequence and sequences of other Mycoplasma species, respectively.
已从支原体PG50 DNA的基因组文库中分离出四个携带rRNA顺反子片段的克隆。通过异源双链和置换环分析,并辅以序列数据,我们证明这四个克隆共同覆盖了支原体PG50的两个rRNA顺反子以及侧翼区域。已对克隆片段的部分进行了详细分析,并得出以下结论。tRNALys和tRNALeu的基因位于rrnA的16S rRNA基因上游约450 bp处。一个至少215个密码子的开放阅读框位于rrnB上游且方向相同。对rrnA的3'侧翼区域分析表明,该操纵子之后没有tRNA基因。在此处也可鉴定出一个开放阅读框,其长度至少为83个密码子,有一个推定的启动子和一个可能的核糖体结合位点。其方向与rrnA相同。尚未确定任何一个开放阅读框的功能。分别将rrnA的23S和5S基因的最后880 bp与相应的枯草芽孢杆菌序列和其他支原体物种的序列进行了比较。