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首页> 外文期刊>Biochemistry >In vitro selection of hairpin ribozymes activated with short oligonucleotides.
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In vitro selection of hairpin ribozymes activated with short oligonucleotides.

机译:短寡核苷酸激活的发夹核酶的体外选择。

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We have carried out an in vitro selection to obtain an allosteric hairpin ribozyme, which has cleavage activity in the presence of an exogenous short oligonucleotide as a regulator. Random sequences were inserted in a region corresponding to the hairpin loop of the ribozyme. After 12 rounds of selection, DNA templates were cloned. Of a total of 34 clones, 18 contained the same sequence, and the obtained hairpin ribozymes showed the cleavage activity specifically in the presence of the regulator oligonucleotide. All of the clones contained sequences complementary to the regulator oligonucleotide. The ribozymes with high cleavage activities gained characteristic hairpin loops at the random domain, which were similar to each other. In the absence of the oligonucleotide, the loop domain within the allosteric ribozyme probably forms a slipped hairpin loop, and the complementary sequence, with the regulator oligonucleotide located at the single stranded loop, would allow easy access of the oligonucleotide. The binding of the regulator oligonucleotide triggers a structural change of the hairpin loop to form an active conformation. Furthermore, we constructed an allosteric hammerhead ribozyme by introducing the characteristic hairpin loop. The modified hammerhead ribozyme was also changed to an allosteric ribozyme, which was activated by the addition of the regulator oligonucleotide. The characteristic hairpin loop, which was proved to be regulated by an exogenous oligonucleotide in this report, may be used to control RNA functions in various fields.
机译:我们已经进行了体外选择以获得变构发夹状核酶,其在外源短寡核苷酸作为调节剂的存在下具有切割活性。将随机序列插入对应于核酶发夹环的区域。经过12轮选择后,克隆了DNA模板。在总共34个克隆中,有18个包含相同的序列,并且所获得的发夹状核酶在调节寡核苷酸的存在下特异性地显示了切割活性。所有克隆均包含与调节寡核苷酸互补的序列。具有高裂解活性的核酶在随机域获得了特征性的发夹环,这些环彼此相似。在缺少寡核苷酸的情况下,变构核酶内的环结构域可能会形成一个滑动的发夹环,并且互补序列(调节寡核苷酸位于单链环上)将使寡核苷酸易于进入。调节寡核苷酸的结合触发发夹环的结构变化,以形成活性构象。此外,我们通过引入特征性的发夹环构建了变构锤头状核酶。修饰的锤头状核酶也改变为变构核酶,其通过添加调节剂寡核苷酸而被激活。在本报告中已证明由外源性寡核苷酸调节的发夹状特征环可用于控制各个领域的RNA功能。

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