Simpson Craig G, Jennings S Nikki, Clark Gillian P, Thow Graham, Brown John W S
Gene Expression, Scottish Crop Research Institute, Invergowrie, Dundee, DD2 5DA Scotland, UK.
Plant J. 2004 Jan;37(1):82-91. doi: 10.1046/j.1365-313x.2003.01941.x.
In potato invertase genes, the constitutively included, 9-nucleotide (nt)-long mini-exon requires a strong branchpoint and U-rich polypyrimidine tract for inclusion. The strength of these splicing signals was demonstrated by greatly enhanced splicing of a poorly spliced intron and by their ability to support splicing of an artificial mini-exon, following their introduction. Plant introns also require a second splicing signal, UA-rich intronic elements, for efficient intron splicing. Mutation of the branchpoint caused loss of mini-exon inclusion without loss of splicing enhancement, showing that the same U-rich sequence can function as either a polypyrimidine tract or a UA-rich intronic element. The distinction between the splicing signals depended on intron context (the presence or absence of an upstream, adjacent and functional branchpoint), and on the sequence context of the U-rich elements. Polypyrimidine tracts tolerated C residues while UA-rich intronic elements tolerated As. Thus, in plant introns, U-rich splicing elements can have dual roles as either a general plant U-rich splicing signal or a polypyrimidine tract. Finally, overexpression of two different U-rich binding proteins enhanced intron recognition significantly. These results highlight the importance of co-operation between splicing signals, the importance of other nucleotides within U-rich elements for optimal binding of competing splicing factors and effects on splicing efficiency of U-rich binding proteins.
在马铃薯转化酶基因中,组成型包含的9个核苷酸(nt)长的小外显子需要一个强分支点和富含U的多嘧啶序列才能被包含。通过显著增强一个剪接效率低的内含子的剪接以及在引入这些剪接信号后它们支持人工小外显子剪接的能力,证明了这些剪接信号的强度。植物内含子还需要第二个剪接信号,即富含UA的内含子元件,以实现高效的内含子剪接。分支点的突变导致小外显子包含缺失但剪接增强没有丧失,这表明相同的富含U的序列既可以作为多嘧啶序列,也可以作为富含UA的内含子元件发挥作用。剪接信号之间的区别取决于内含子背景(上游、相邻且功能性分支点的存在与否)以及富含U的元件的序列背景。多嘧啶序列耐受C残基,而富含UA的内含子元件耐受A残基。因此,在植物内含子中,富含U的剪接元件可以作为一般的植物富含U的剪接信号或多嘧啶序列发挥双重作用。最后,两种不同的富含U的结合蛋白的过表达显著增强了内含子识别。这些结果突出了剪接信号之间合作的重要性、富含U的元件内其他核苷酸对于竞争性剪接因子最佳结合的重要性以及富含U的结合蛋白对剪接效率的影响。