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VS核酶催化亚结构域的鉴定及活性位点环中显著序列耐受性的证据。

Identification of the catalytic subdomain of the VS ribozyme and evidence for remarkable sequence tolerance in the active site loop.

作者信息

Sood Vanita D, Collins Richard A

机构信息

Department of Molecular and Medical Genetics, University of Toronto, Ontario, Canada M5S 1A8, USA.

出版信息

J Mol Biol. 2002 Jul 12;320(3):443-54. doi: 10.1016/s0022-2836(02)00521-1.

Abstract

We show here that the ribozyme domain of the Neurospora VS ribozyme consists of separable upper and lower subdomains. Deletion analysis demonstrates that the entire upper subdomain (helices III/IV/V) is dispensable for site-specific cleavage activity, providing experimental evidence that the active site is contained within the lower subdomain and within the substrate itself. We demonstrate an important role in cleavage activity for a region of helix VI called the 730 loop. Surprisingly, several loop sequences, sizes, and structures at this position can support site-specific cleavage, suggesting that a variety of non-Watson-Crick structures, rather than a specific loop structure, in this region of the ribozyme can contribute to formation of the active site.

摘要

我们在此表明,粗糙脉孢菌VS核酶的核酶结构域由可分离的上、下子结构域组成。缺失分析表明,整个上子结构域(螺旋III/IV/V)对于位点特异性切割活性是可有可无的,这提供了实验证据,证明活性位点包含在下子结构域和底物本身内。我们证明了螺旋VI中一个称为730环的区域在切割活性中起重要作用。令人惊讶的是,该位置的几个环序列、大小和结构都能支持位点特异性切割,这表明核酶该区域的多种非沃森-克里克结构,而非特定的环结构,可有助于活性位点的形成。

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