Sugisaki H, Takanami M
Institute for Chemical Research, Kyoto University, Japan.
J Biol Chem. 1993 Jan 15;268(2):887-91.
We analyzed the chimeric guide RNA (gRNA)-mRNA molecules in Crithidia fasciculata that are predicted to transiently exist in editing of the 5'-terminal domain of apocytochrome b (CYb) mRNA, by polymerase chain reaction amplification and DNA sequencing, and obtained evidence suggesting that among the 14 editing sites numbered from 3' to 5', the sequence in the 3'-half of the sites (3' block) was specified by one guide RNA species (gRNA-I) and that in the remaining half of the sites (5' block) by the other guide RNA species (gRNA-II) and that the direction of editing in each block was 3' to 5'. The predicted transition site of editing by two gRNAs was between the first and second U residues from the 3' end within editing site 7. We found that a stretch of the edited sequence in the 3' block of mRNA could form a stable duplex with a stretch immediately upstream of the guide sequence in gRNA-II. The result leads to a successive editing model that the 3' block of pre-edited mRNA is first edited by gRNA-I, and after completion of editing, the 5' portion of gRNA-II pairs with the edited mRNA for editing of the 5' block.
我们通过聚合酶链反应扩增和DNA测序,分析了在克氏锥虫中预测会短暂存在于脱辅基细胞色素b(CYb)mRNA 5'-末端结构域编辑过程中的嵌合向导RNA(gRNA)-mRNA分子,并获得了证据,表明在从3'到5'编号的14个编辑位点中,位点3'半部分(3'块)的序列由一种向导RNA种类(gRNA-I)指定,其余位点半部分(5'块)的序列由另一种向导RNA种类(gRNA-II)指定,并且每个块中的编辑方向是从3'到5'。两种gRNA编辑的预测转换位点在编辑位点7中从3'端起的第一个和第二个U残基之间。我们发现,mRNA的3'块中的一段编辑序列可以与gRNA-II中向导序列紧邻上游的一段序列形成稳定的双链体。该结果导致了一个连续编辑模型,即预编辑mRNA的3'块首先由gRNA-I编辑,编辑完成后,gRNA-II的5'部分与编辑后的mRNA配对以编辑5'块。