HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Single-polarity recombinant adeno-associated virus 2 vector-mediated transgene expression in vitro and in vivo: mechanism of transduction.

Abstract
Recombinant adeno-associated virus 2 (AAV) vectors encapsidate single-stranded genomes of either polarity equally frequently in separate mature virions. Because viral genomes of either polarity are transcriptionally inactive, both the failure to undergo viral second-strand DNA synthesis and the failure to undergo DNA strand annealing have been proposed as possible reasons to account for the observed low efficiency of transgene expression. We compared the transduction efficiencies of conventional AAV vectors containing both [-] and [+] polarity genomes with those containing either the [-] or the [+] polarity genomes, in vitro as well as in vivo. We document that the transduction efficiency of single-polarity AAV vectors is significantly enhanced by (i) co-infection with adenovirus; (ii) small interfering RNA (siRNA)-mediated down-modulation of a cellular protein, FKBP52, tyrosine-phosphorylated forms of which inhibit AAV second-strand DNA synthesis; (iii) over-expression of a cellular protein tyrosine phosphatase, T cell protein tyrosine phosphatase (TC-PTP), which catalyzes tyrosine-dephosphorylation of FKBP52; and (iv) deliberate over-expression of TC-PTP, or the absence of FKBP52, respectively, in TC-PTP-transgenic mice and in FKBP52-knockout mice. These data confirm that viral second-strand DNA synthesis, rather than DNA strand annealing, is the rate-limiting step in efficient transduction by AAV vectors. This finding has implications in the use of these vectors in human gene therapy.
AuthorsLi Zhong, Xiaohuai Zhou, Yanjun Li, Keyun Qing, Xiao Xiao, Richard Jude Samulski, Arun Srivastava
JournalMolecular therapy : the journal of the American Society of Gene Therapy (Mol Ther) Vol. 16 Issue 2 Pg. 290-5 (Feb 2008) ISSN: 1525-0024 [Electronic] United States
PMID18087261 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
Chemical References
  • RNA, Small Interfering
  • Tacrolimus Binding Proteins
  • tacrolimus binding protein 4
Topics
  • Animals
  • Blotting, Northern
  • Blotting, Southern
  • Cell Line, Tumor
  • Dependovirus (genetics)
  • Genetic Vectors (genetics)
  • HeLa Cells
  • Humans
  • Mice
  • Models, Theoretical
  • RNA, Small Interfering (genetics)
  • Tacrolimus Binding Proteins (genetics, physiology)
  • Transduction, Genetic
  • Transgenes (genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: