McPheeters D S
Department of Biochemistry, Case Western Reserve University, School of Medicine, Cleveland, Ohio 44106-4935, USA.
RNA. 1996 Nov;2(11):1110-23.
The small nuclear RNA (snRNA) components of the spliceosome have been proposed to catalyze the excision of introns from nuclear pre-mRNAs. If this hypothesis is correct, then the snRNA components of the spliceosome may interact directly with the reactive groups of pre-mRNA substrates. To explore this possibility, a genetic screen has been used to identify potential interactions between the U6 RNA and the pre-mRNA branch site. Notably, the selection yielded mutants in two regions of the yeast U6 RNA implicated previously in the catalytic events of splicing. These mutants significantly increase the splicing of pre-mRNA substrates containing non-adenosine branch sites. U6 mutants in U2/U6 helix Ia show strong allele-specific interactions with the branch site nucleotide and interact with PRP16, a factor implicated previously in branch site utilization. The other mutants cluster in the intramolecular helix of U6 and suppress the effects of branch site mutations in a nonallele-specific fashion. The locations of these mutants may define positions important for binding of the U6 intramolecular helix to the catalytic core of the spliceosome.
剪接体的小核RNA(snRNA)组分被认为可催化从核前体mRNA中切除内含子。如果这一假说是正确的,那么剪接体的snRNA组分可能会直接与前体mRNA底物的反应基团相互作用。为了探究这种可能性,已利用遗传筛选来鉴定U6 RNA与前体mRNA分支位点之间的潜在相互作用。值得注意的是,筛选在酵母U6 RNA的两个区域产生了突变体,这两个区域先前被认为与剪接的催化事件有关。这些突变体显著增加了含有非腺苷分支位点的前体mRNA底物的剪接。U2/U6螺旋Ia中的U6突变体与分支位点核苷酸表现出强烈的等位基因特异性相互作用,并与PRP16相互作用,PRP16是一种先前被认为与分支位点利用有关的因子。其他突变体聚集在U6的分子内螺旋中,并以非等位基因特异性方式抑制分支位点突变的影响。这些突变体的位置可能确定了U6分子内螺旋与剪接体催化核心结合的重要位置。