Weiss-Brummer B, Holl J, Schweyen R J, Rödel G, Kaudewitz F
Cell. 1983 May;33(1):195-202. doi: 10.1016/0092-8674(83)90348-3.
Revertants have been obtained from six mutants of the box9 cluster, which are supposed to be defective in RNA splicing as a result of alterations in a splice signal sequence. This sequence is in the 5' part of intron 4 of the cob gene, 330 to 340 bp downstream from the 5' splice site. Sequencing reveals that reversion to splicing competence is achieved by restoration of the wild-type box9 sequence; by creation of novel box9 sequences; and by introduction of a second site or suppressor mutation (sup-) compensating for the effect of the primary box9- mutation. The sup- mutation alters a sequence in intron 4,293 bp upstream from the box9- primary mutation. The box9 sequence and this upstream sequence can base pair to form an intramolecular hybrid in intron RNA in which box9- and sup- are compensatory base pair exchanges (G----A and C----U, respectively). Thus intramolecular hybrid structures of intron RNA are essential for RNA splicing.
已从box9基因簇的六个突变体中获得了回复突变体,这些突变体由于剪接信号序列的改变而被认为在RNA剪接方面存在缺陷。该序列位于cob基因内含子4的5'部分,在5'剪接位点下游330至340 bp处。测序显示,回复到剪接活性是通过恢复野生型box9序列、创建新的box9序列以及引入第二个位点或抑制突变(sup-)来补偿最初的box9突变的影响来实现的。sup-突变改变了box9主要突变上游293 bp处内含子4中的一个序列。box9序列和这个上游序列可以碱基配对,在内含子RNA中形成分子内杂交体,其中box9-和sup-是互补的碱基对交换(分别为G----A和C----U)。因此,内含子RNA的分子内杂交结构对于RNA剪接至关重要。