首页> 美国卫生研究院文献>Nucleic Acids Research >Intra-RNA cross-linking in Escherichia coli 30S ribosomal subunits: selective isolation of cross-linked products by hybridization to specific cDNA fragments.
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Intra-RNA cross-linking in Escherichia coli 30S ribosomal subunits: selective isolation of cross-linked products by hybridization to specific cDNA fragments.

机译:大肠杆菌30S核糖体亚基中的RNA内交联:通过与特定cDNA片段杂交来选择性分离交联产物。

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摘要

M13 clones were constructed with cDNA inserts corresponding to specific regions of E. coli ribosomal RNA. The DNA from the clones was immobilized by coupling to diazobenzyloxymethyl cellulose, and was used for the selective isolation by hybridization of cross-linked RNA complexes containing the complementary sequences. Immobilized DNA samples with inserts complementary to four different regions covering bases 735-1384 of the 16S RNA were hybridized with a mixture of 16S RNA fragments generated by partial digestion of 30S subunits that had been cross-linked by ultraviolet irradiation in vivo. After dehybridization, the individual RNA fragments and cross-linked complexes were separated by gel electrophoresis and analysed by our usual procedures. Nine cross-links are described; four of these are hitherto unobserved "secondary structural" cross-links, and one is a new "tertiary structural" cross-link between positions 243-247 and 891-894 of the 16S RNA.
机译:用对应于大肠杆菌核糖体RNA特定区域的cDNA插入片段构建M13克隆。来自克隆的DNA通过偶联至重氮苄氧基甲基纤维素而被固定,并通过杂交包含互补序列的交联RNA复合物用于选择性分离。将具有与覆盖16S RNA的碱基735-1384的四个不同区域互补的插入物的固定化DNA样品与通过部分消化30S亚基而产生的16S RNA片段的混合物进行杂交,该30S亚基已通过体内紫外线照射进行了交联。脱杂交后,通过凝胶电泳分离各个RNA片段和交联的复合物,并通过我们的常规程序进行分析。描述了九个交联键。这些中的四个是迄今为止从未观察到的“二级结构”交联,一个是16S RNA的243-247和891-894位之间的新“三级结构”交联。

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