Literature DB >> 1731072

Sequence and structure of the catalytic RNA of hepatitis delta virus genomic RNA.

H N Wu1, Y J Wang, C F Hung, H J Lee, M M Lai.   

Abstract

Human hepatitis delta virus (HDV) RNA has been shown to contain a self-catalyzed cleavage activity. The sequence requirement for its catalytic activity appears to be different from that of other known ribozymes. In this paper, we define the minimum contiguous sequence and secondary structure of the HDV genomic RNA required for the catalytic activity. By using nested-set deletion mutants, we have determined that the essential sequence for the catalytic activity is contained within no more than 85 nucleotides of HDV RNA. These results are in close agreement with the previous determinations and confirmed the relative insignificance of the sequence at the 5' side of the cleavage site. The smallest catalytic RNA, representing HDV genomic RNA nucleotide positions 683 to 770, was used as the basis for studying the secondary structure requirements for catalytic activity. Analysis of the RNA structure, using RNase V1, nuclease S1 and diethylpyrocarbonate treatments showed that this RNA contains at least two stem-and-loop structures. Other larger HDV RNA subfragments containing the catalytic activity also have a very similar secondary structure. By performing site-specific mutagenesis studies, it was shown that one of the stem-and-loop structures could be deleted to half of its original size without affecting the catalytic activity. In addition, the other stem-and-loop contained a six base-pair helix, and the structure, rather than the sequence, of this helix was required for the catalytic activity. However, the structure of a portion of the stem-and-loop remains uncertain. We also report that this RNA can be divided into two separate molecules, which alone did not have cleavage activity but, when mixed, one of the RNAs could be cleaved in trans. This study thus reveals some features of the secondary structure of the HDV genomic RNA involved in self-catalyzed cleavage. A model of this RNA structure is presented.

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Year:  1992        PMID: 1731072     DOI: 10.1016/0022-2836(92)90728-3

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  24 in total

1.  Analysis of the cleavage reaction of a trans-acting human hepatitis delta virus ribozyme.

Authors:  H Fauzi; J Kawakami; F Nishikawa; S Nishikawa
Journal:  Nucleic Acids Res       Date:  1997-08-01       Impact factor: 16.971

2.  Ribozyme-based gene-inactivation systems require a fine comprehension of their substrate specificities; the case of delta ribozyme.

Authors:  Lucien Junior Bergeron; Jonathan Ouellet; Jean-Pierre Perreault
Journal:  Curr Med Chem       Date:  2003-12       Impact factor: 4.530

3.  Mutagenesis analysis of the self-cleavage domain of hepatitis delta virus antigenomic RNA.

Authors:  H N Wu; Z S Huang
Journal:  Nucleic Acids Res       Date:  1992-11-25       Impact factor: 16.971

4.  Random mutations to evaluate the role of bases at two important single-stranded regions of genomic HDV ribozyme.

Authors:  P K Kumar; Y A Suh; H Miyashiro; F Nishikawa; J Kawakami; K Taira; S Nishikawa
Journal:  Nucleic Acids Res       Date:  1992-08-11       Impact factor: 16.971

5.  Determination of the secondary structure of and cellular protein binding to the 3'-untranslated region of the hepatitis C virus RNA genome.

Authors:  T Ito; M M Lai
Journal:  J Virol       Date:  1997-11       Impact factor: 5.103

6.  Imino proton NMR analysis of HDV ribozymes: nested double pseudoknot structure and Mg2+ ion-binding site close to the catalytic core in solution.

Authors:  Yoichiro Tanaka; Tamaki Hori; Mitsuhiro Tagaya; Taiichi Sakamoto; Yasuyuki Kurihara; Masato Katahira; Seiichi Uesugi
Journal:  Nucleic Acids Res       Date:  2002-02-01       Impact factor: 16.971

7.  Core-associated non-duplex sequences distinguishing the genomic and antigenomic self-cleaving RNAs of hepatitis delta virus.

Authors:  T S Wadkins; M D Been
Journal:  Nucleic Acids Res       Date:  1997-10-15       Impact factor: 16.971

8.  Local helix content and RNA-binding activity of the N-terminal leucine-repeat region of hepatitis delta antigen.

Authors:  J W Cheng; I J Lin; Y C Lou; M T Pai; H N Wu
Journal:  J Biomol NMR       Date:  1998-07       Impact factor: 2.835

9.  A pseudoknot ribozyme structure is active in vivo and required for hepatitis delta virus RNA replication.

Authors:  K S Jeng; A Daniel; M M Lai
Journal:  J Virol       Date:  1996-04       Impact factor: 5.103

10.  Nuclear localization signals, but not putative leucine zipper motifs, are essential for nuclear transport of hepatitis delta antigen.

Authors:  M F Chang; S C Chang; C I Chang; K Wu; H Y Kang
Journal:  J Virol       Date:  1992-10       Impact factor: 5.103

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