Walker T A, Johnson K D, Olsen G J, Peters M A, Pace N R
Biochemistry. 1982 May 11;21(10):2320-9. doi: 10.1021/bi00539a008.
Secondary structure mapping experiments using S1 nuclease, RNase T1, and diethyl pyrocarbonate as conformational probes have identified those regions in mouse 5.8S rRNA containing major sites of interaction with 28S rRNA. One site encompasses the 3'-terminal 20 nucleotides and corresponds to the region identified previously as a component of an RNase-resistant 5.8S/28S rRNA junction complex. A second site, located at the 5' terminus, has not been defined precisely but is believed to involve approximately 20--30 nucleotides. The existence of these sites of interaction is supported by comparing sequences of eukaryotic 5.8S and 28S rRNA with those of the prokaryotic 23S rRNA. Evidence for the occurrence of at least three helical regions in the central portion of the mouse 5.8S rRNA molecule is also presented.
使用S1核酸酶、核糖核酸酶T1和焦碳酸二乙酯作为构象探针进行的二级结构映射实验,已确定了小鼠5.8S核糖体RNA中与28S核糖体RNA相互作用主要位点所在的区域。一个位点包含3'末端的20个核苷酸,对应于先前被鉴定为核糖核酸酶抗性5.8S/28S核糖体RNA连接复合体组成部分的区域。第二个位点位于5'末端,尚未精确界定,但据信涉及约20 - 30个核苷酸。通过比较真核生物5.8S和28S核糖体RNA与原核生物23S核糖体RNA的序列,支持了这些相互作用位点的存在。本文还提供了小鼠5.8S核糖体RNA分子中部至少三个螺旋区域存在的证据。