Literature DB >> 18707243

A triplex ribozyme expression system based on a single hairpin ribozyme.

Guillermo Aquino-Jarquin1, María Luisa Benítez-Hess, Joseph A DiPaolo, Luis M Alvarez-Salas.   

Abstract

Triplex ribozyme (RZ) configurations allow for the individual activity of trans-acting RZs in multiple expression cassettes (multiplex), thereby increasing target cleavage relative to conventionally expressed RZs. Although hairpin RZs have been advantageously compared to hammerhead RZs, their longer size and structural features complicated triplex design. We present a triplex expression system based on a single hairpin RZ with transcleavage capability and simple engineering. The system was tested in vitro using cis- and trans-cleavage kinetic assays against a known target RNA from HPV-16 E6/E7 mRNA. Single and multiplex triplex RZ constructs were more efficient in cleaving the target than tandem-cloned hairpin RZs, suggesting that the release of individual RZs enhanced trans-cleavage kinetics. Multiplex systems constructed with two different hairpin RZs resulted in better trans-cleavage compared to standard double-RZ constructs. In addition, the triplex RZ performed cis- and trans-cleavage in cervical cancer cells. The use of triplex configurations with multiplex RZs permit differential targeting of the same or different RNA, thus improving potential use against unstable targets. This prototype will provide the basis for the development of future RZ-based therapies and technologies.

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Year:  2008        PMID: 18707243      PMCID: PMC2966833          DOI: 10.1089/oli.2008.0130

Source DB:  PubMed          Journal:  Oligonucleotides        ISSN: 1545-4576


  23 in total

Review 1.  The hairpin ribozyme: structure, assembly and catalysis.

Authors:  N G Walter; J M Burke
Journal:  Curr Opin Chem Biol       Date:  1998-02       Impact factor: 8.822

2.  Folding of the four-way RNA junction of the hairpin ribozyme.

Authors:  F Walter; A I Murchie; D M Lilley
Journal:  Biochemistry       Date:  1998-12-15       Impact factor: 3.162

3.  Factors governing the activity in vivo of ribozymes transcribed by RNA polymerase III.

Authors:  S Koseki; T Tanabe; K Tani; S Asano; T Shioda; Y Nagai; T Shimada; J Ohkawa; K Taira
Journal:  J Virol       Date:  1999-03       Impact factor: 5.103

4.  The loop B domain is physically separable from the loop A domain in the hairpin ribozyme.

Authors:  C Shin; J N Choi; S I Song; J T Song; J H Ahn; J S Lee; Y D Choi
Journal:  Nucleic Acids Res       Date:  1996-07-15       Impact factor: 16.971

5.  Inhibition of HPV-16 E6/E7 immortalization of normal keratinocytes by hairpin ribozymes.

Authors:  L M Alvarez-Salas; A E Cullinan; A Siwkowski; A Hampel; J A DiPaolo
Journal:  Proc Natl Acad Sci U S A       Date:  1998-02-03       Impact factor: 11.205

6.  Inhibition of HIV-1 replication by retroviral vectors expressing monomeric and multimeric hammerhead ribozymes.

Authors:  A Ramezani; S F Ding; S Joshi
Journal:  Gene Ther       Date:  1997-08       Impact factor: 5.250

7.  Design of hairpin ribozymes for in vitro and cellular applications.

Authors:  Q Yu; J M Burke
Journal:  Methods Mol Biol       Date:  1997

Review 8.  The hairpin ribozyme: discovery, two-dimensional model, and development for gene therapy.

Authors:  A Hampel
Journal:  Prog Nucleic Acid Res Mol Biol       Date:  1998

9.  A multifunctional expression vector for an anti-HIV-1 ribozyme that produces a 5'- and 3'-trimmed trans-acting ribozyme, targeted against HIV-1 RNA, and cis-acting ribozymes that are designed to bind to and thereby sequester trans-activator proteins such as Tat and Rev.

Authors:  N Yuyama; J Ohkawa; T Koguma; M Shirai; K Taira
Journal:  Nucleic Acids Res       Date:  1994-11-25       Impact factor: 16.971

10.  Triple ribozyme-mediated down-regulation of the retinoblastoma gene.

Authors:  C M Benedict; W Pan; S E Loy; G A Clawson
Journal:  Carcinogenesis       Date:  1998-07       Impact factor: 4.944

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