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Informational Complexity and Functional Activity of RNA Structures

机译:RNA结构的信息复杂性和功能活性

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摘要

Very little is known about the distribution of functional DNA, RNA, and protein molecules in sequence space. The question of how the number and complexity of distinct solutions to a particular biochemical problem varies with activity is an important aspect of this general problem. Here we present a comparison of the structures and activities of eleven distinct GTP-binding RNAs (aptamers). By experimentally measuring the amount of information required to specify each optimal binding structure, we show that defining a structure capable of 10-fold tighter binding requires approximately 10 additional bits of information. This increase in information content is equivalent to specifying the identity of five additional nucleotide positions and corresponds to an ~1000-fold decrease in abundance in a sample of random sequences. We observe a similar relationship between structural complexity and activity in a comparison of two catalytic RNAs (ribozyme ligases), raising the possibility of a general relationship between the complexity of RNA structures and their functional activity. Describing how information varies with activity in other heteropolymers, both biological and synthetic, may lead to an objective means of comparing their functional properties. This approach could be useful in predicting the functional utility of novel heteropolymers.
机译:关于功能性DNA,RNA和蛋白质分子在序列空间中的分布知之甚少。解决特定生化问题的不同解决方案的数量和复杂性如何随活动而变化的问题是此一般问题的重要方面。在这里,我们提出了十一种不同的GTP结合RNA(适体)的结构和活性的比较。通过实验测量指定每个最佳绑定结构所需的信息量,我们显示出定义能够进行10倍更紧密绑定的结构需要大约10个附加信息位。信息含量的这种增加等同于指定了另外五个核苷酸位置的同一性,并且对应于随机序列样本中的丰度降低了约1000倍。我们在两个催化RNA(核酶连接酶)的比较中观察到结构复杂性和活性之间的相似关系,从而增加了RNA结构的复杂性与其功能活性之间一般关系的可能性。描述信息如何随生物和合成的其他杂聚物中的活性变化而变化,可能导致比较它们的功能特性的客观手段。这种方法可能对预测新型杂聚物的功能有用。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2004年第16期|p. 5130-5137|共8页
  • 作者单位

    Howard Hughes Medical Institute and Department of Molecular Biology, Massachusetts General Hospital, Boston, MA, 02114;

    Howard Hughes Medical Institute and Department of Molecular Biology, Massachusetts General Hospital, Boston, MA, 02114;

    EMD-Lexigen Pharmaceuticals, 45A Middlesex Turnpike, Billerica, MA 01821;

    Howard Hughes Medical Institute and Department of Molecular Biology, Massachusetts General Hospital, Boston, MA, 02114;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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