Rose Alan B
Molecular and Cellular Biology, University of California, Davis, California, 95616, USA.
RNA. 2002 Nov;8(11):1444-53. doi: 10.1017/s1355838202020551.
To explore possible mechanisms of intron-mediated enhancement of gene expression, the features of PAT1 intron 1 required to elevate mRNA accumulation were systematically tested in transgenic Arabidopsis. This intron is remarkably resilient, retaining some ability to increase mRNA accumulation when splicing was prevented by mutation of 5' and 3' splice sites, branchpoint sequences, or when intron U-richness was reduced. Enhancement was abolished by simultaneously eliminating branchpoints and the 5' splice site, structures involved in the first two steps of spliceosome assembly. Although this suggests that the splicing machinery is required, intron splicing is clearly not enough to enhance mRNA accumulation. Five other introns were all efficiently spliced but varied widely in their ability to increase mRNA levels. Furthermore, PAT1 intron 1 was spliced but lost the ability to elevate mRNA accumulation when moved to the 3' UTR. These findings demonstrate that splicing per se is neither necessary nor sufficient for an intron to enhance mRNA accumulation, and suggest a mechanism that requires intron recognition by the splicing machinery but also involves nonconserved intron sequences.
为了探究内含子介导的基因表达增强的可能机制,在转基因拟南芥中系统测试了提高mRNA积累所需的PAT1内含子1的特征。该内含子具有显著的弹性,当5'和3'剪接位点、分支点序列发生突变阻止剪接时,或者当内含子富含尿嘧啶的程度降低时,仍保留一定增加mRNA积累的能力。通过同时消除分支点和5'剪接位点(这两个结构参与剪接体组装的前两步),增强作用被消除。虽然这表明需要剪接机制,但内含子剪接显然不足以增强mRNA积累。其他五个内含子都能有效剪接,但在增加mRNA水平的能力上差异很大。此外,PAT1内含子1被剪接,但当移至3'非翻译区时失去了提高mRNA积累的能力。这些发现表明,剪接本身对于内含子增强mRNA积累既不是必需的也不是充分的,并提示了一种机制,该机制需要剪接机制识别内含子,但也涉及非保守的内含子序列。