A nested double pseudoknot is required for self-cleavage activity of both the genomic and antigenomic hepatitis delta virus ribozymes

被引:84
作者
Wadkins, TS
Perrotta, AT
Ferré-D'Amaré, AR
Doudna, JA
Been, MD [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Biochem, Durham, NC 27710 USA
[2] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[3] Yale Univ, Howard Hughes Med Inst, New Haven, CT 06520 USA
关键词
catalytic; RNA; hepatitis delta virus; RNA structure; self-cleaving RNA;
D O I
10.1017/S1355838299990209
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The crystal structure of a;genomic hepatitis delta virus (HDV) ribozyme 3' cleavage product predicts the existence of a 2 bp duplex, P1.1, that had not been previously identified in the HDV ribozymes. P1.1 consists of two canonical C-G base: pairs stacked beneath the G.U wobble pair at the cleavage site and would appear-to pull together critical structural elements of the ribozyme. P1.1 is the second Stem of a second pseudoknot in. the ribozyme, making the overall fold of the ribozyme a nested double pseudoknot Sequence comparison suggests the potential for P1.1 and a similar fold in the antigenomic ribozyme. In this study, the base pairing requirements of P1.1 for cleavage activity were tested in both the genomic and antigenomic HDV ribozymes by mutagenesis. In both sequences, cleavage activity was severely reduced when mismatches were introduced into P1.1, but restored when alternative base pairing combinations were incorporated. Thus, P1.1 is an essential: structural element required for cleavage of both the genomic and antigenomic HDV ribozymes and the model for the antigenomic ribozyme secondary structure should also be modified to include P1.1.
引用
收藏
页码:720 / 727
页数:8
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