Stiege W, Kosack M, Stade K, Brimacombe R
Max-Planck-Institut für Molekulare Genetik, Abteilung Wittmann, Berlin-Dahlem, FRG.
Nucleic Acids Res. 1988 May 25;16(10):4315-29. doi: 10.1093/nar/16.10.4315.
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.
构建了M13克隆,其cDNA插入片段对应于大肠杆菌核糖体RNA的特定区域。克隆的DNA通过与重氮苄氧基甲基纤维素偶联而固定化,并用于通过杂交选择性分离含有互补序列的交联RNA复合物。将具有与覆盖16S RNA的735 - 1384位碱基的四个不同区域互补的插入片段的固定化DNA样品,与通过对体内经紫外线照射交联的30S亚基进行部分消化而产生的16S RNA片段混合物杂交。去杂交后,通过凝胶电泳分离各个RNA片段和交联复合物,并按我们常用的方法进行分析。描述了九个交联;其中四个是迄今未观察到的“二级结构”交联,一个是16S RNA的243 - 247位和891 - 894位之间新的“三级结构”交联。