Neĭlin M U, Nigul A I, Toots I E, Saarma M Iu
Bioorg Khim. 1987 Jan;13(1):128-30.
Two small RNA fragments, 5,3S and 4,7S, were observed in gel electrophoretic analysis of RNA of the 40S ribosomal subunit of rat liver. 5,3S RNA (134-136 nucleotides long) proved to be 5'-terminal fragment of 18S ribosomal RNA, whereas 4,7 RNA is the degradation product of 5,3S RNA with 27-28 5'-terminal nucleotides lost. The secondary structure of 5,3S RNA was probed with two structure-specific nucleases, S1 nuclease and the double-strand specific cobra venom endoribonuclease. The nuclease digestion data agree well with the computer generated secondary structure model for 5,3S RNA. This model predicts that the 5'-terminal part of rat liver ribosomal 18S RNA forms an independent structural domain. The affinity chromatography experiments with the immobilized 5,3S fragment show that 5,3S RNA does not bind rat liver ribosomal proteins.
在大鼠肝脏40S核糖体亚基RNA的凝胶电泳分析中观察到两个小RNA片段,即5.3S和4.7S。5.3S RNA(长度为134 - 136个核苷酸)被证明是18S核糖体RNA的5'末端片段,而4.7S RNA是5.3S RNA的降解产物,丢失了27 - 28个5'末端核苷酸。用两种结构特异性核酸酶,即S1核酸酶和双链特异性眼镜蛇毒核糖核酸内切酶探测了5.3S RNA的二级结构。核酸酶消化数据与计算机生成的5.3S RNA二级结构模型非常吻合。该模型预测大鼠肝脏核糖体18S RNA的5'末端部分形成一个独立的结构域。用固定化的5.3S片段进行的亲和层析实验表明,5.3S RNA不结合大鼠肝脏核糖体蛋白。