Literature DB >> 2261458

Self-cleavage of hepatitis delta virus genomic strand RNA is enhanced under partially denaturing conditions.

S P Rosenstein1, M D Been.   

Abstract

Self-cleavage of a polyribonucleotide containing an autocleaving sequence from the genomic strand of hepatitis delta virus was enhanced by conditions that destabilized RNA structure. Self-cleavage of the transcripts used in this study required Mg2+ (or another divalent cation), and in the absence of denaturants, maximum cleavage was observed at very low Mg2+ concentrations (0.05-0.1 mM). However, at 37 degrees C and in the presence of 2-10 mM Mg2+ the rate of cleavage was increased as much as 50-fold with the addition of urea to 5 M or formamide to 10 M. Cleavage was prevented by higher concentrations of the same reagents (9.5 M urea or 22.5 M formamide), presumably because a structure required for self-cleavage is disrupted by strongly denaturing conditions. In contrast to a previous report [Wu, H.-N., & Lai, M. M. C. (1989) Science 243, 652-654], we find that chelating Mg2+ with EDTA terminates the cleavage reaction without promoting measurable amounts of ligation of the cleavage products. The ability of denaturants to promote rapid self-cleavage in vitro raises the possibility that an unidentified factor could have a similar effect in vivo.

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Year:  1990        PMID: 2261458     DOI: 10.1021/bi00487a002

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  27 in total

1.  A host-specific function is required for ligation of a wide variety of ribozyme-processed RNAs.

Authors:  C E Reid; D W Lazinski
Journal:  Proc Natl Acad Sci U S A       Date:  2000-01-04       Impact factor: 11.205

2.  A versatile communication module for controlling RNA folding and catalysis.

Authors:  Alexis Kertsburg; Garrett A Soukup
Journal:  Nucleic Acids Res       Date:  2002-11-01       Impact factor: 16.971

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.  Deletion of internal sequence on the HDV-ribozyme: elucidation of functionally important single-stranded loop regions.

Authors:  Y A Suh; P K Kumar; F Nishikawa; E Kayano; S Nakai; O Odai; S Uesugi; K Taira; S Nishikawa
Journal:  Nucleic Acids Res       Date:  1992-02-25       Impact factor: 16.971

6.  The self-cleaving domain from the genomic RNA of hepatitis delta virus: sequence requirements and the effects of denaturant.

Authors:  A T Perrotta; M D Been
Journal:  Nucleic Acids Res       Date:  1990-12-11       Impact factor: 16.971

7.  Non-ribozyme sequences enhance self-cleavage of ribozymes derived from Hepatitis delta virus.

Authors:  M G Belinsky; G Dinter-Gottlieb
Journal:  Nucleic Acids Res       Date:  1991-02-11       Impact factor: 16.971

8.  Alternative tertiary structure attenuates self-cleavage of the ribozyme in the satellite RNA of barley yellow dwarf virus.

Authors:  W A Miller; S L Silver
Journal:  Nucleic Acids Res       Date:  1991-10-11       Impact factor: 16.971

9.  Wild-type is the optimal sequence of the HDV ribozyme under cotranscriptional conditions.

Authors:  Durga M Chadalavada; Andrea L Cerrone-Szakal; Philip C Bevilacqua
Journal:  RNA       Date:  2007-10-23       Impact factor: 4.942

10.  RNA-mediated ligation of self-cleavage products of a Neurospora mitochondrial plasmid transcript.

Authors:  B J Saville; R A Collins
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-01       Impact factor: 11.205

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