Bulygin K N, Popugaeva E A, Repkova M N, Meshchaninova M I, Ven'iaminova A G, Gaĭfer D M, Frolova L Iu, Karpova G G
Mol Biol (Mosk). 2007 Sep-Oct;41(5):858-67.
Positioning of stop codon and the adjacent triplet downstream of it with respect to the components of human 80S termination complex was studied with the use of mRNA analogues that bore stop signal UPuPuPu (Pu is A or G) and photoactivatable perfluoroaryl azide group. This group was attached to one of nucleotides of the stop signal or 3' of it (in positions +4 to +9 with respect to the first nucleotide of the P site codon). It was shown that upon mild UV irradiation the mRNA analogues crosslinked to components of model complexes imitating state of 80S ribosome in the course of translation termination. It was found that termination factors eRF1 and eRF3 do not affect mutual arrangement of stop signal and the 18S rRNA. Factor eRF1 was shown to cross-link to modified nucleotides in positions +5 to +9 (ability of eRF1 to cross-link to stop codon nucleotide in position +4 was shown earlier). Fragments of eRF1 containing cross-linking sites of the mRNA analogues were determined. In fragment 52-195 (containing the N-domain and a part of the M-domain) we have found cross-linking sites of the analogues that bore modifying groups on A or G in positions +5 to +9 or at the terminal phosphate of nucleotide in position +7. For mRNA analogues bearing modifying groups on G site of cross-linking from positions +5 to +7 was found in the eRF1 fragment
利用携带终止信号UPuPuPu(Pu为A或G)以及可光活化的全氟芳基叠氮基团的mRNA类似物,研究了终止密码子及其下游相邻三联体相对于人80S终止复合物各组分的定位情况。该基团连接在终止信号的一个核苷酸上或其3'端(相对于P位点密码子的第一个核苷酸,位于+4至+9位)。结果表明,在温和紫外线照射下,mRNA类似物与模拟翻译终止过程中80S核糖体状态的模型复合物的组分发生交联。研究发现,终止因子eRF1和eRF3不影响终止信号与18S rRNA的相互排列。已证明因子eRF1与+5至+9位的修饰核苷酸发生交联(先前已表明eRF1能够与+4位的终止密码子核苷酸发生交联)。确定了含有mRNA类似物交联位点的eRF1片段。在片段52 - 195(包含N结构域和部分M结构域)中,我们发现了在+5至+9位的A或G上带有修饰基团或在+7位核苷酸的末端磷酸基团上带有修饰基团的类似物的交联位点。对于在+5至+7位的交联G位点上带有修饰基团的mRNA类似物,在eRF1片段中也有发现