Morales J, Borrero M, Sumerel J, Santiago C
University of Puerto Rico, Department of Biology, San Juan 00931-3360.
DNA Seq. 1997;7(5):243-59. doi: 10.3109/10425179709034044.
A PCR approach was used to isolate repeated U5 small nuclear RNA (snRNA) genes from the sea urchin Lytechinus variegatus. A 1.3 kb repeat, LvU5.0, and three other variants, LvU5.1-U5.3, that differ in the coding region and in the proximal sequence element (PSE) region were isolated. Southern Blot analysis indicate that the U5 snRNA genes, unlike other embryonically expressed snRNA genes (U1, U2 and U6), are not found in a simple tandem repeat, but instead, exist in several heterogeneous clusters each with a small number of genes. The U5 PSE has limited sequence similarity with the other sea urchin PSEs. However, when used in a mobility shift assay the U5 PSE forms a protein/DNA complex that is very similar to the complex formed with the U6 PSE. An RNase protection assay used to monitor the accumulation of U5 snRNA during development shows that at least two U5 variants are coordinately expressed during embryogenesis.
采用聚合酶链式反应(PCR)方法从多色刺海胆(Lytechinus variegatus)中分离重复的U5小核RNA(snRNA)基因。分离出一个1.3 kb的重复序列LvU5.0以及其他三个变体LvU5.1 - U5.3,它们在编码区和近端序列元件(PSE)区域存在差异。Southern印迹分析表明,与其他胚胎表达的snRNA基因(U1、U2和U6)不同,U5 snRNA基因并非以简单串联重复的形式存在,而是存在于几个异质簇中,每个簇中有少量基因。U5 PSE与其他海胆PSE的序列相似性有限。然而,在迁移率变动分析中,U5 PSE形成的蛋白质/DNA复合物与U6 PSE形成的复合物非常相似。用于监测发育过程中U5 snRNA积累的核糖核酸酶保护分析表明,在胚胎发生过程中至少有两个U5变体协同表达。