Brown J W, Feix G, Frendewey D
EMBO J. 1986 Nov;5(11):2749-58. doi: 10.1002/j.1460-2075.1986.tb04563.x.
Two plant introns along with flanking exon sequences have been isolated from an amylase gene of wheat and a legumin gene of pea and cloned behind the phage SP6 promoter. Pre-mRNAs produced by in vitro transcription with SP6 RNA polymerase were tested for their ability to be spliced in a HeLa cell nuclear extract. The plant introns were accurately spliced and the predicted splice junctions were used. Lariat RNAs were observed as both intermediates and final products during the splicing reaction. The branch points were mapped to adenosine residues lying within sequences that showed good homology to the animal branch point consensus. Consensus sequences for the 5' and 3' splice junctions and for putative branch point sequences of plants were derived from an analysis of 168 plant intron sequences.
从小麦的淀粉酶基因和豌豆的豆球蛋白基因中分离出两个植物内含子及其侧翼外显子序列,并克隆到噬菌体SP6启动子的下游。用SP6 RNA聚合酶进行体外转录产生的前体mRNA在HeLa细胞核提取物中进行剪接能力测试。植物内含子被准确剪接,并使用了预测的剪接位点。在剪接反应过程中,套索状RNA被观察为中间产物和最终产物。分支点被定位到与动物分支点共有序列具有良好同源性的腺苷残基上。通过对168个植物内含子序列的分析,得出了植物5'和3'剪接位点以及推定分支点序列的共有序列。