首页> 外文期刊>Journal of Molecular Biology >IDENTIFICATION OF FUNCTIONAL DOMAINS IN THE SELF-CLEAVING NEUROSPORA VS RIBOZYME USING DAMAGE SELECTION
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IDENTIFICATION OF FUNCTIONAL DOMAINS IN THE SELF-CLEAVING NEUROSPORA VS RIBOZYME USING DAMAGE SELECTION

机译:利用损伤选择识别自切神经元VS核酶中的功能域

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摘要

Varkud Satellite (VS) RNA contains a small self-cleaving RNA motif that is distinct in its sequence and secondary structure from the hammerhead, hairpin, and hepatitis delta virus ribozymes, which are found in other natural RNAs. We have used a base specific chemical damage selection (modification interference) assay to identify functionally important nucleotides and structural elements in VS RNA. Many modified bases interfered with self-cleavage and most of these clustered at helix junctions, certain internal loops, and in a long-range pseudoknot; these correspond to previously determined sites of magnesium-dependent protection from chemical modification. The clustering suggests that these bases are important not only for a large number of individual interactions, but because they form a smaller number of structural elements that are important for activity. Modification of bases in other single-stranded regions, which did not exhibit magnesium-dependent protection, generally did not interfere with activity, suggesting that some of these regions might be dispensable for function. Surprisingly, we found a separate cluster of bases whose modification significantly enhanced cleavage. These bases appear to form a structural element that naturally attenuates the self-cleavage reaction. In natural VS RNA this attenuator structure may affect the cleavage/ligation equilibrium by inhibiting circle re-opening, thereby helping to maintain the RNA in a circular form, which is the predominant form of VS RNA in vivo. Taken together, the results of the damage selection experiments localize the catalytic core of VS RNA to a small subset of the previously determined minimal contiguous sequence. (C) 1997 Academic Press Limited. [References: 28]
机译:Varkud卫星(VS)RNA包含一个小的自我切割RNA基序,其序列和二级结构与其他天然RNA中发现的锤头状,发夹状和丙型肝炎三角洲病毒核酶不同。我们已使用碱基特异性化学损伤选择(修饰干扰)测定法来鉴定VS RNA中功能上重要的核苷酸和结构元件。许多修饰的碱基干扰了自身裂解,并且大多数碱基聚集在螺旋连接处,某些内部环和远距离的假结中。这些对应于先前确定的镁依赖性保护免受化学修饰的位点。聚类表明,这些碱基不仅对于大量的个体相互作用非常重要,而且因为它们形成了对活动重要的较少数量的结构元素。其他未显示镁依赖性保护作用的单链区域中的碱基修饰通常不会干扰活性,这表明其中某些区域可能对功能没有作用。令人惊讶地,我们发现了一个单独的碱基簇,其修饰显着增强了切割。这些碱基似乎形成了自然减弱自切割反应的结构元件。在天然VS RNA中,这种减毒剂结构可能会通过抑制环的重新开放而影响切割/连接平衡,从而有助于将RNA保持为环状,而环状是体内VS RNA的主要形式。两者合计,损伤选择实验的结果将VS RNA的催化核心定位到先前确定的最小连续序列的一小部分。 (C)1997 Academic Press Limited。 [参考:28]

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