Spieth J, Brooke G, Kuersten S, Lea K, Blumenthal T
Department of Biology, Indiana University, Bloomington 47405.
Cell. 1993 May 7;73(3):521-32. doi: 10.1016/0092-8674(93)90139-h.
The mRNAs of six C. elegans genes are known to be trans-spliced to SL2. We report here that a similarly oriented gene is located 100-300 bp upstream of each. We present evidence that the genes in these clusters are cotranscribed and downstream mRNAs are formed by cleavage at the polyadenylation site and trans-splicing. From one three-gene cluster we isolated cDNA clones representing both polycistronic RNAs and mRNAs polyadenylated at the free 3' end created by trans-splicing, suggesting that polycistronic RNAs can be processed by trans-splicing. Several experiments indicate that SL2 trans-splicing is a consequence of a gene's downstream location in an operon. In particular, when an SL1-accepting gene was moved to a downstream location, its mRNA was trans-spliced largely to SL2. The possible regulatory significance of cotranscription of C. elegans genes is discussed.
已知六种秀丽隐杆线虫基因的mRNA会被反式剪接至SL2。我们在此报告,每个基因上游100 - 300 bp处都有一个方向相似的基因。我们提供的证据表明,这些基因簇中的基因是共转录的,下游mRNA是通过在聚腺苷酸化位点切割和反式剪接形成的。从一个三基因簇中,我们分离出了代表多顺反子RNA和通过反式剪接产生的游离3'端聚腺苷酸化的mRNA的cDNA克隆,这表明多顺反子RNA可以通过反式剪接进行加工。多项实验表明,SL2反式剪接是基因在操纵子中位于下游的结果。特别是,当一个接受SL1的基因移至下游位置时,其mRNA大部分会被反式剪接至SL2。本文还讨论了秀丽隐杆线虫基因共转录可能具有的调控意义。