Newman A
MRC Laboratory of Molecular Biology, MRC Centre, Cambridge, UK.
EMBO J. 1987 Dec 1;6(12):3833-9. doi: 10.1002/j.1460-2075.1987.tb02720.x.
In experiments involving deletion and rearrangement of intron sequences two small regions of the intron in the yeast CYH2 ribosomal protein gene were found to play important roles in splicing of the pre-mRNA. One element lies downstream of the 5' splice site, and the other is upstream of the branchpoint sequence UACUAAC. Deletion of the element upstream of the branchpoint prevents spliceosome formation and blocks splicing in vivo and in vitro. Deletion of the element downstream of the 5' splice site does not on its own block splicing but rescues spliceosome formation and splicing of pre-mRNA lacking the element upstream of the branchpoint. These elements correspond to two regions of sequence complementarity which are a conserved feature of the introns in yeast pre-mRNAs. Mixing and matching of the elements from the ACT1 and CYH2 gene introns showed that these elements can cooperate in an intron-specific fashion to control spliceosome assembly.
在涉及内含子序列缺失和重排的实验中,发现酵母CYH2核糖体蛋白基因内含子的两个小区域在pre - mRNA剪接中起重要作用。一个元件位于5'剪接位点下游,另一个位于分支点序列UACUAAC上游。分支点上游元件的缺失会阻止剪接体形成,并在体内和体外阻断剪接。5'剪接位点下游元件的缺失本身并不阻断剪接,但能挽救缺乏分支点上游元件的pre - mRNA的剪接体形成和剪接。这些元件对应于两个序列互补区域,这是酵母pre - mRNA内含子的一个保守特征。来自ACT1和CYH2基因内含子的元件的混合与匹配表明,这些元件可以以内含子特异性方式协同控制剪接体组装。