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来自人类病原体丁型肝炎病毒的顺式和反式作用核酶。

Cis- and trans-acting ribozymes from a human pathogen, hepatitis delta virus.

作者信息

Been M D

机构信息

Department of Biochemistry, Duke University Medical Center, Durham, NC 27710.

出版信息

Trends Biochem Sci. 1994 Jun;19(6):251-6. doi: 10.1016/0968-0004(94)90151-1.

Abstract

Hepatitis delta virus (HDV) contains two self-cleaving RNA sequences (ribozymes) that may naturally function as such in human cells. A pseudo-knot-containing structural motif, which is distinct from the well-characterized secondary structures of self-cleaving RNAs common to the plant pathogenic RNAs, is shared by the cis-acting HDV ribozymes. Definition of the sequences and secondary structures of the HDV ribozymes has facilitated the design of novel catalytic molecules, such as small RNA circles, capable of site-specific cleavage of RNA in trans.

摘要

丁型肝炎病毒(HDV)含有两个自我切割RNA序列(核酶),它们可能在人类细胞中自然发挥此类功能。顺式作用的HDV核酶具有一种含假结的结构基序,该结构基序不同于植物致病RNA中常见的自我切割RNA的特征性二级结构。HDV核酶的序列和二级结构的确定促进了新型催化分子的设计,如能够反式对RNA进行位点特异性切割的小RNA环。

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