Hoadley Kelly A, Purtha Whitney E, Wolf Amanda C, Flynn-Charlebois Amber, Silverman Scott K
Department of Chemistry, University of Illinois at Urbana-Champaign, 600 South Mathews Avenue, Urbana, Illinois 61801, USA.
Biochemistry. 2005 Jun 28;44(25):9217-31. doi: 10.1021/bi050146g.
We report Zn(2+)-dependent deoxyribozymes that ligate RNA. The DNA enzymes were identified by in vitro selection and ligate RNA with k(obs) up to 0.5 min(-)(1) at 1 mM Zn(2+) and 23 degrees C, pH 7.9, which is substantially faster than our previously reported Mg(2+)-dependent deoxyribozymes. Each new Zn(2+)-dependent deoxyribozyme mediates the reaction of a specific nucleophile on one RNA substrate with a 2',3'-cyclic phosphate on a second RNA substrate. Some of the Zn(2+)-dependent deoxyribozymes create native 3'-5' RNA linkages (with k(obs) up to 0.02 min(-)(1)), whereas all of our previous Mg(2+)-dependent deoxyribozymes that use a 2',3'-cyclic phosphate create non-native 2'-5' RNA linkages. On this basis, Zn(2+)-dependent deoxyribozymes have promise for synthesis of native 3'-5'-linked RNA using 2',3'-cyclic phosphate RNA substrates, although these particular Zn(2+)-dependent deoxyribozymes are likely not useful for this practical application. Some of the new Zn(2+)-dependent deoxyribozymes instead create non-native 2'-5' linkages, just like their Mg(2+) counterparts. Unexpectedly, other Zn(2+)-dependent deoxyribozymes synthesize one of three unnatural linkages that are formed upon the reaction of an RNA nucleophile other than a 5'-hydroxyl group. Two of these unnatural linkages are the 3'-2' and 2'-2' linear junctions created when the 2'-hydroxyl of the 5'-terminal guanosine of one RNA substrate attacks the 2',3'-cyclic phosphate of the second RNA substrate. The third unnatural linkage is a branched RNA that results from attack of a specific internal 2'-hydroxyl of one RNA substrate at the 2',3'-cyclic phosphate. When compared with the consistent creation of 2'-5' linkages by Mg(2+)-dependent ligation, formation of this variety of RNA ligation products by Zn(2+)-dependent deoxyribozymes highlights the versatility of transition metals such as Zn(2+) for mediating nucleic acid catalysis.
我们报道了能连接RNA的锌离子依赖性脱氧核酶。这些DNA酶是通过体外筛选鉴定出来的,在1 mM锌离子、23摄氏度、pH 7.9的条件下,它们连接RNA的观测速率常数(k(obs))高达0.5 min⁻¹,这比我们之前报道的镁离子依赖性脱氧核酶快得多。每个新的锌离子依赖性脱氧核酶介导一个RNA底物上特定亲核试剂与另一个RNA底物上的2',3'-环磷酸酯的反应。一些锌离子依赖性脱氧核酶能形成天然的3'-5' RNA连接(k(obs)高达0.02 min⁻¹),而我们之前所有使用2',3'-环磷酸酯的镁离子依赖性脱氧核酶都会形成非天然的2'-5' RNA连接。在此基础上,锌离子依赖性脱氧核酶有望利用2',3'-环磷酸酯RNA底物合成天然的3'-5'-连接RNA,尽管这些特定的锌离子依赖性脱氧核酶可能对这一实际应用并无用处。一些新的锌离子依赖性脱氧核酶反而会形成非天然的2'-5'连接,就像它们的镁离子对应物一样。出乎意料的是,其他锌离子依赖性脱氧核酶会合成三种非天然连接中的一种,这些连接是由除5'-羟基以外的RNA亲核试剂反应形成的。其中两种非天然连接是当一个RNA底物5'-末端鸟苷的2'-羟基攻击第二个RNA底物的2',3'-环磷酸酯时形成的3'-2'和2'-2'线性连接。第三种非天然连接是一种分支RNA,它是由一个RNA底物特定的内部2'-羟基攻击2',3'-环磷酸酯产生的。与镁离子依赖性连接一致产生2'-5'连接相比,锌离子依赖性脱氧核酶形成这种多样的RNA连接产物凸显了锌离子等过渡金属在介导核酸催化方面的多功能性。