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Antisense-induced guanine quadruplexes inhibit reverse transcription by HIV-1 reverse transcriptase.
Hagihara, Masaki; Yamauchi, Lisa; Seo, Akiko; Yoneda, Keisuke; Senda, Mayo; Nakatani, Kazuhiko.
Afiliação
  • Hagihara M; Department of Regulatory Bioorganic Chemistry, The Institute of Scientific and Industrial Research, Osaka University, Ibaraki 567-0047, Osaka, Japan.
J Am Chem Soc ; 132(32): 11171-8, 2010 Aug 18.
Article em En | MEDLINE | ID: mdl-20698683
ABSTRACT
Guanine quadruplex structures in DNA and RNA affect normal cellular processes such as replication, recombination, and translation. Thus, controlling guanine quadruplex structures could make it possible to manipulate the biological function of nucleic acids. Here, we report a novel antisense strategy using guanine-tethered antisense oligonucleotides (g-ASs) that introduces an RNA-DNA heteroquadruplex structure on RNA templates in a predictable and sequence-specific manner, which in practice effectively inhibited reverse transcription on a variety of RNA sequences, including the HIV-1 RNA genome. Reverse transcriptase-mediated enzymatic analysis, together with other biophysical analyses, elucidated a cooperative binding of duplex and quadruplex in g-AS-RNA complexes. The remarkable ability of g-ASs to inhibit reverse transcription could make possible the development of novel anti-retroviral gene therapies based on blocking the replication of RNA genomes to complementary DNA, which is a critical step for integration into the host's genome.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oligonucleotídeos Antissenso / HIV-1 / Transcrição Reversa / Transcriptase Reversa do HIV / Quadruplex G Idioma: En Revista: J Am Chem Soc Ano de publicação: 2010 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oligonucleotídeos Antissenso / HIV-1 / Transcrição Reversa / Transcriptase Reversa do HIV / Quadruplex G Idioma: En Revista: J Am Chem Soc Ano de publicação: 2010 Tipo de documento: Article País de afiliação: Japão