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The ends of a large RNA molecule are necessarily close.

机译:大RNA分子的末端必须紧密相连。

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We show on general theoretical grounds that the two ends of single-stranded (ss) RNA molecules (consisting of roughly equal proportions of A, C, G and U) are necessarily close together, largely independent of their length and sequence. This is demonstrated to be a direct consequence of two generic properties of the equilibrium secondary structures, namely that the average proportion of bases in pairs is ~60% and that the average duplex length is ~4. Based on mfold and Vienna computations on large numbers of ssRNAs of various lengths (1000-10000 nt) and sequences (both random and biological), we find that the 5'-3' distance-defined as the sum of H-bond and covalent (ss) links separating the ends of the RNA chain-is small, averaging 15-20 for each set of viral sequences tested. For random sequences this distance is ~12, consistent with the theory. We discuss the relevance of these results to evolved sequence complementarity and specific protein binding effects that are known to be important for keeping the two ends of viral and messenger RNAs in close proximity. Finally we speculate on how our conclusions imply indistinguishability in size and shape of equilibrated forms of linear and covalently circularized ssRNA molecules.
机译:我们从一般的理论基础上证明,单链(ss)RNA分子的两端(由大约相等比例的A,C,G和U组成)必须彼此靠近,这在很大程度上与它们的长度和序列无关。证明这是平衡二级结构的两个一般性质的直接结果,即成对碱基的平均比例为〜60%,平均双链体长度为〜4。基于mfold和Vienna对大量不同长度(1000-10000 nt)和序列(随机和生物学)ssRNA的计算,我们发现5'-3'距离定义为H键和共价键的总和分开RNA链末端的(ss)链接很小,每组被测病毒序列平均15-20。对于随机序列,此距离约为12,与理论一致。我们讨论了这些结果与进化的序列互补性和特定蛋白质结合作用的相关性,众所周知,这些作用对于保持病毒RNA和信使RNA的两端非常接近非常重要。最后,我们推测我们的结论如何暗示线性和共价环化的ssRNA分子平衡形式的大小和形状没有可分辨性。

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