Vary C P, Vournakis J N
J Biol Chem. 1984 Mar 10;259(5):3299-307.
A general method is described for the removal of 3'-terminal polyadenylate tracts from eukaryotic messenger RNA to generate essentially homogeneous length products that can be 3'-end labeled and sequenced. Hybridization of specific oligodeoxyribonucleotides was used to direct ribonuclease H to the junction of the 3'-noncoding region and the polyadenylate sequence of rabbit alpha and beta globin mRNAs. Site-specific deadenylylation of both globin mRNAs is demonstrated by partial enzymatic sequence analysis following 3'-terminal labeling with 5'-pCp (where p indicates the labeled phosphate group). The secondary structure of the 3'-noncoding region is studied by enzymatic digestion with S1 nuclease and cobra venom ribonuclease. Structural features of the 3'-noncoding regions of these mRNAs are described, including the protein synthesis termination and the poly(A) addition recognition sites.
描述了一种从真核生物信使RNA中去除3'末端聚腺苷酸序列的通用方法,以产生基本上长度均一的产物,这些产物可进行3'末端标记和测序。使用特定的寡脱氧核糖核苷酸杂交来引导核糖核酸酶H作用于兔α和β珠蛋白mRNA的3'非编码区与聚腺苷酸序列的交界处。在用5'-pCp(其中p表示标记的磷酸基团)进行3'末端标记后,通过部分酶促序列分析证明了两种珠蛋白mRNA的位点特异性去腺苷酸化。用S1核酸酶和眼镜蛇毒核糖核酸酶进行酶切消化研究了3'非编码区的二级结构。描述了这些mRNA的3'非编码区的结构特征,包括蛋白质合成终止和聚(A)添加识别位点。