Fischel J L, Krol A, Ehresmann C, Fellner P, Ebel J P
Biochimie. 1975;57(8):885-97. doi: 10.1016/s0300-9084(75)80211-2.
We have studied the primary structure of 16S ribosomal RNA from Proteus vulgaris. The oligonucleotides containing methylated bases appeared to be the same as those of Escherichia coli, with one exception. We have also studied the base composition of the oligonucleotides obtained after T1 ribonuclease digestion of 16S RNA. On the basis both of their position on the fingerprint and of their pancreatic ribonuclease analyses, approximately 25 appeared to differ from those found in the E. coli T1 fingerprints. From the isolation of large fragments arising from the action of endogeneous endonucleases, we have concluded that the RNA sequences of both species are very similar. We have shown that the 5' and 3' extremities of 16S RNA are mostly conserved. It appears that the regions which are known to interact with ribosomal proteins in E. coli (particularly S8 and S15) are also less modified. It is noteworthy that the sequence modifications which have been observed are clustered and often correspond to regions of heterogeneity in E. coli 16S RNA.
我们研究了普通变形杆菌16S核糖体RNA的一级结构。含甲基化碱基的寡核苷酸似乎与大肠杆菌的相同,只有一个例外。我们还研究了用T1核糖核酸酶消化16S RNA后得到的寡核苷酸的碱基组成。基于它们在指纹图谱上的位置以及它们的胰核糖核酸酶分析,大约25种似乎与大肠杆菌T1指纹图谱中发现的不同。从内源性核酸内切酶作用产生的大片段的分离中,我们得出结论,这两个物种的RNA序列非常相似。我们已经表明,16S RNA的5'和3'末端大多是保守的。已知在大肠杆菌中与核糖体蛋白相互作用的区域(特别是S8和S15)似乎也较少被修饰。值得注意的是,观察到的序列修饰是成簇的,并且常常对应于大肠杆菌16S RNA中的异质性区域。