Wassarman D A, Steitz J A
Department of Molecular Biophysics and Biochemistry, Yale University School of Medicine, Haven, CT 06536.
Science. 1992 Sep 25;257(5078):1918-25. doi: 10.1126/science.1411506.
Precursor messenger RNA splicing requires multiple factors including U1, U2, U4, U5, and U6 small nuclear RNA's. The crosslinking reagent psoralen was used to analyze the interactions of these RNA's with an adenovirus precursor messenger RNA in HeLa nuclear extract. An endogenous U2-U4-U6 crosslinkable complex dissociated upon incubation with precursor messenger RNA. During splicing, U1, U2, U5, and U6 became crosslinked to precursor messenger RNA and U2, U5, and U6 became crosslinked to excised lariat intron. U2 also formed a doubly crosslinked complex with U6 and precursor messenger RNA. The U1, U5, and U6 crosslinks to the precursor messenger RNA mapped to intron sequences near the 5' splice site, whereas the U2 crosslink mapped to the branch site. The kinetics of crosslink formation and disappearance delineates a temporal pathway for the action of small RNA's in the spliceosome. Potential base pairing interactions between conserved sequences in the small nuclear RNA's and precursor messenger RNA at the sites of crosslinking suggest that the 5' splice site is defined in several steps prior to the first cleavage event.
前体信使核糖核酸剪接需要多种因子,包括U1、U2、U4、U5和U6小核核糖核酸。交联剂补骨脂素用于分析这些核糖核酸与HeLa细胞核提取物中腺病毒前体信使核糖核酸的相互作用。一种内源性的U2-U4-U6可交联复合物在与前体信使核糖核酸孵育时解离。在剪接过程中,U1、U2、U5和U6与前体信使核糖核酸发生交联,U2、U5和U6与切除的套索状内含子发生交联。U2还与U6和前体信使核糖核酸形成了双重交联复合物。U1、U5和U6与前体信使核糖核酸的交联定位在5'剪接位点附近的内含子序列上,而U2的交联定位在分支位点。交联形成和消失的动力学描绘了小核糖核酸在剪接体中作用的时间途径。小核核糖核酸和前体信使核糖核酸在交联位点的保守序列之间潜在的碱基配对相互作用表明,5'剪接位点在第一次切割事件之前是分几步确定的。