Hartshorne T, Agabian N
School of Pharmacy, University of California, San Francisco 94143-1204.
Genes Dev. 1990 Dec;4(12A):2121-31. doi: 10.1101/gad.4.12a.2121.
A new model of U2 RNA secondary structure has been developed by comparing U2 RNA sequences from distantly related trypanosomatids, which process their RNAs by trans-splicing, and U2 RNAs from cis-splicing organisms. The trypanosomatid U2 RNA retains structural similarity in important functional domains of cis-splicing U2 RNAs yet differs from previous consensus models in that only two helices, rather than three, can form in the stem-loop II region. This alteration eliminates the capacity for pseudoknot formation and produces a single-stranded region 3' to stem-loop II, which may be accessible for snRNP protein binding. Trypanosomatid U2 RNAs differ in the putative branchpoint recognition sequences, which completely diverge from the conserved GUAGUA consensus of cis-splicing organisms.
通过比较来自远缘锥虫(其通过反式剪接加工RNA)的U2 RNA序列和顺式剪接生物体的U2 RNA,开发了一种新的U2 RNA二级结构模型。锥虫的U2 RNA在顺式剪接U2 RNA的重要功能域中保留了结构相似性,但与先前的共有模型不同,因为在茎环II区域只能形成两个螺旋,而不是三个。这种改变消除了假结形成的能力,并在茎环II的3'端产生了一个单链区域,该区域可能可供snRNP蛋白结合。锥虫的U2 RNA在假定的分支点识别序列上有所不同,该序列与顺式剪接生物体保守的GUAGUA共有序列完全不同。