Query C C, Strobel S A, Sharp P A
Department of Biology, Massachusetts Institute of Technology, Cambridge, 02139-4307, USA.
EMBO J. 1996 Mar 15;15(6):1392-402.
An adenosine at the branch site, the nucleophile for the first transesterification step of splicing, is nearly invariant in mammalian pre-mRNA introns. The chemical groups on the adenine base were varied systematically and assayed for formation of early spliceosome complexes and execution of the first and second steps of splicing. Recognition of constituents of the adenine is critical in formation of a U2 snRNP-containing complex on a minimal branch-site oligonucleotide. Furthermore, the efficiencies of the first and second chemical steps have different dependencies on the functional groups of the adenine. In total, the chemical groups on the adenine base at the branch site are differentially recognized during at least three different processes in the splicing of pre-mRNA. Moreover, a protein, p14, interacts with the adenine in a base-specific fashion and may mediate early recognition of this base.
位于分支位点的腺苷,作为剪接第一步转酯反应的亲核试剂,在哺乳动物前体mRNA内含子中几乎是不变的。对腺嘌呤碱基上的化学基团进行了系统的改变,并检测了早期剪接体复合物的形成以及剪接第一步和第二步的执行情况。腺嘌呤成分的识别对于在最小分支位点寡核苷酸上形成含U2 snRNP的复合物至关重要。此外,第一步和第二步化学反应的效率对腺嘌呤功能基团有不同的依赖性。总体而言,在前体mRNA剪接的至少三个不同过程中,分支位点腺嘌呤碱基上的化学基团受到不同的识别。此外,一种蛋白质p14以碱基特异性方式与腺嘌呤相互作用,可能介导对该碱基的早期识别。