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10S RNA的特性:一种来自大肠杆菌的新型稳定RNA分子。

Characterization of 10S RNA: a new stable rna molecule from Escherichia coli.

作者信息

Ray B K, Apirion D

出版信息

Mol Gen Genet. 1979 Jul 2;174(1):25-32. doi: 10.1007/BF00433301.

Abstract

When cells of Escherichia coli are labeled with 32Pi for long periods of time and the cell content is subjected to electrophoresis in polyacrylamide gels, an RNA band appears which is about 10S in size. This band seems to contain three conformers. After treatment with formamide only a single band appears in this region of the gel, which contains 550 nucleotides as determined from its mobility. The complexity of the fingerprint of this material, after digestion with T1-RNase, is in agreement with the size as determined by the mobility, this confirming that indeed it is a single molecule. Composition of the T1-oligonucleotides was determined by digesting the T1-generated oligonucleotides with pancreatic RNase and T2-RNase. The quantitative and qualitative analysis of these digestions suggest that 10S RNA contains 609 nucleotides. The molecule contains, besides the four regular bases, one copy per molecule of the modified base pseudouridine. 10S RNA cannot be processed by cell extracts to tRNA-sized molecules and does not bind significantly to ribosomes, hence it is unlikely to be a tRNA precursor or an mRNA.

摘要

当用³²P i长时间标记大肠杆菌细胞,并使其细胞内容物在聚丙烯酰胺凝胶中进行电泳时,会出现一条大小约为10S的RNA条带。这条带似乎包含三种构象体。用甲酰胺处理后,凝胶的该区域仅出现一条带,根据其迁移率测定,该带含有550个核苷酸。用T1核糖核酸酶消化后,这种物质指纹图谱的复杂性与由迁移率测定的大小一致,这证实它确实是一个单分子。通过用胰核糖核酸酶和T2核糖核酸酶消化T1产生的寡核苷酸来确定T1寡核苷酸的组成。这些消化的定量和定性分析表明,10S RNA含有609个核苷酸。该分子除了含有四种常规碱基外,每分子还含有一个修饰碱基假尿苷。10S RNA不能被细胞提取物加工成tRNA大小的分子,也不与核糖体显著结合,因此它不太可能是tRNA前体或mRNA。

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