Copertino D W, Christopher D A, Hallick R B
Department of Molecular and Cellular Biology, University of Arizona, Tucson 85721.
Nucleic Acids Res. 1991 Dec 11;19(23):6491-7. doi: 10.1093/nar/19.23.6491.
The splicing of a 409 nucleotide intron from the Euglena gracilis chloroplast ribosomal protein S3 gene (rps3) was examined by cDNA cloning and sequencing, and northern hybridization. Based on the characterization of a partially spliced pre-mRNA, the intron was characterized as a 'mixed' twintron, composed of a 311 nucleotide group II intron internal to a 98 nucleotide group III intron. Twintron excision is via a 2-step sequential splicing pathway, with removal of the internal group II intron preceding excision of the external group III intron. Based on secondary structural analysis of the twintron, we propose that group III introns may represent highly degenerate versions of group II introns. The existence of twintrons is interpreted as evidence that group II introns were inserted during the evolution of Euglena chloroplast genes from a common ancestor with eubacteria, archaebacteria, cyanobacteria, and other chloroplasts.
通过cDNA克隆、测序以及Northern杂交,对纤细裸藻叶绿体核糖体蛋白S3基因(rps3)中一个409个核苷酸的内含子的剪接进行了研究。基于对部分剪接的前体mRNA的特征分析,该内含子被鉴定为一个“混合”双内含子,由一个98个核苷酸的III类内含子内部的311个核苷酸的II类内含子组成。双内含子的切除是通过两步连续剪接途径进行的,内部II类内含子的切除先于外部III类内含子的切除。基于对双内含子的二级结构分析,我们提出III类内含子可能代表II类内含子的高度退化形式。双内含子的存在被解释为II类内含子是在纤细裸藻叶绿体基因从与真细菌、古细菌、蓝细菌和其他叶绿体的共同祖先进化过程中插入的证据。