Pitt Jason N, Ferré-D'Amaré Adrian R
Molecular and Cellular Biology Program, University of Washington, Seattle, Washington 98195, USA.
J Am Chem Soc. 2009 Mar 18;131(10):3532-40. doi: 10.1021/ja8067325.
Ribozyme-catalyzed RNA synthesis is central to the RNA world hypothesis. No natural RNA polymerase ribozymes have been discovered. However, ribozymes that catalyze the requisite chemistry, generating a new phosphodiester through attack of a terminal hydroxyl of an RNA on the alpha-phosphate of a triphosphate-activated oligonucleotide, have been isolated by in vitro selection. These experiments often yield ribozymes that generate 2'-5' phosphodiesters rather than conventional 3'-5' linkages. We have determined crystal structures of the duplex formed by the template segment of a representative 2'-5' RNA ligase ribozyme, the class II ligase, and its ligation product. The structures reveal a product-template duplex with a G x A pair at the ligation junction. This sheared pair is flanked on one side by a minor groove-broadening wedge comprised of two unpaired nucleotides. The reported structure of an independently isolated 3'-5' ligase ribozyme, the L1 ligase, shows a product-template duplex that shares the G x A pair with the class II ligase. However, this G x A pair is flanked by G x U wobbles, rather than an unpaired wedge. We demonstrate that these structural differences of the substrate-template duplexes are largely responsible for the divergent regioselectivity of the two ribozymes, independent of their catalytic moieties, by constructing chimeras. The L1 ligase with a class II substrate-template duplex shows a 30-fold increase in 2'-5' bond synthesis, while the class II ligase with an L1 substrate-template duplex produces 3'-5' bonds exclusively. These results demonstrate how local geometry inherent to the substrate-template duplexes controls the regioselectivity of ribozyme-catalyzed RNA ligation reactions.
核酶催化的RNA合成是RNA世界假说的核心。尚未发现天然的RNA聚合酶核酶。然而,通过体外筛选已分离出能催化必要化学反应的核酶,即通过RNA的末端羟基攻击三磷酸激活的寡核苷酸的α-磷酸来生成新的磷酸二酯键。这些实验常常产生生成2'-5'磷酸二酯键而非传统3'-5'连接的核酶。我们已经确定了一种代表性的2'-5'RNA连接酶核酶(II类连接酶)的模板片段与其连接产物形成的双链体的晶体结构。这些结构揭示了在连接位点具有G×A碱基对的产物-模板双链体。这个错配碱基对的一侧由一个由两个未配对核苷酸组成的小沟拓宽楔形结构所环绕。已报道的一种独立分离的3'-5'连接酶核酶(L1连接酶)的结构显示,其产物-模板双链体与II类连接酶共享G×A碱基对。然而,这个G×A碱基对两侧是G×U摆动碱基对,而非未配对的楔形结构。我们通过构建嵌合体证明,底物-模板双链体的这些结构差异在很大程度上决定了这两种核酶不同的区域选择性,而与它们的催化部分无关。具有II类底物-模板双链体的L1连接酶在2'-5'键合成方面增加了30倍,而具有L1底物-模板双链体的II类连接酶则只产生3'-5'键。这些结果证明了底物-模板双链体固有的局部几何结构如何控制核酶催化的RNA连接反应的区域选择性。