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Resistance of human hepatitis delta virus RNAs to dicer activity
Journal article   Open access   Peer reviewed

Resistance of human hepatitis delta virus RNAs to dicer activity

Jinhong Chang, Patrick Provost and John M Taylor
Journal of virology, v 77(22), pp 11910-11917
01 Nov 2003
PMID: 14581527
url
https://doi.org/10.1128/JVI.77.22.11910-11917.2003View
Published, Version of Record (VoR)Open Access (License Unspecified) Open

Abstract

Genome, Viral Hepatitis delta Antigens - physiology Hepatitis Delta Virus - genetics Recombinant Proteins - pharmacology Ribonuclease III - pharmacology RNA, Small Interfering - analysis RNA, Viral - chemistry RNA, Viral - metabolism Virus Replication
The endonuclease dicer cleaves RNAs that are 100% double stranded and certain RNAs with extensive but <100% pairing to release approximately 21-nucleotide (nt) fragments. Circular 1,679-nt genomic and antigenomic RNAs of human hepatitis delta virus (HDV) can fold into a rod-like structure with 74% pairing. However, during HDV replication in hepatocytes of human, woodchuck, and mouse origin, no approximately 21-nt RNAs were detected. Likewise, in vitro, purified recombinant dicer gave <0.2% cleavage of unit-length HDV RNAs. Similarly, rod-like RNAs of potato spindle tuber viroid (PSTVd) and avocado sunblotch viroid (ASBVd) were only 0.5% cleaved. Furthermore, when a 66-nt hairpin RNA with 79% pairing, the putative precursor to miR-122, which is an abundant liver micro-RNA, replaced one end of HDV genomic RNA, it was poorly cleaved, both in vivo and in vitro. In contrast, this 66-nt hairpin, in the absence of appended HDV sequences, was >80% cleaved in vitro. Other 66-nt hairpins derived from one end of genomic HDV, PSTVd, or ASBVd RNAs were also cleaved. Apparently, for unit-length RNAs of HDV, PSTVd, and ASBVd, it is the extended structure with <100% base pairing that confers significant resistance to dicer action.

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Web of Science research areas
Virology
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