Evidence map›Paper›PMID 12552015›Full record

ArticleJournal of virology2003

Adeno-associated virus type 2-mediated gene transfer: role of cellular T-cell protein tyrosine phosphatase in transgene expression in established cell lines in vitro and transgenic mice in vivo.

Keyun Qing, Weiming Li, Li Zhong, Mengqun Tan, Jonathan Hansen, Kirsten A Weigel-Kelley, Linyuan Chen, Mervin C Yoder, Arun Srivastava

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.5field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
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  4. Review
  5. Article
  6. Article
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  8. Article
  9. Article
  10. Review
  11. Liver-Directed Adeno-Associated Viral Gene Therapy for Hemophilia.Journal of genetic syndromes & gene therapy · 2012
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. High-efficiency transduction of the mouse retina by tyrosine-mutant AAV serotype vectors.Molecular therapy : the journal of the American Society of Gene Therapy · 2009
    Article
  17. Article
  18. Article
  19. Gene therapy using adeno-associated virus vectors.Clinical microbiology reviews · 2008
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Keyun QingDepartment of Microbiology and Immunology, Walther Oncology Center, Walther Cancer Institute, Indiana University School of Medicine, 635 Barnhill Drive, Indianapolis, IN 46202, USA.
Weiming Li
Li Zhong
Mengqun Tan
Jonathan Hansen
Kirsten A Weigel-Kelley
Linyuan Chen
Mervin C Yoder
Arun Srivastava
Cancer Institute (WIA) · INWalther Cancer Foundation · USIndiana University – Purdue University Indianapolis · US

Funding

BASIC SCIENCE STUDIES ON GENE THERAPY OF BLOOD DISEASEST32HL007910 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI Roland W. Herzog, Reuben Kapur · 1999 to 2026
$7.6M
ENDOTHELIAL CELL ROLE IN YOLK SAC STEM CELL DEVELOPMENTR01HL063169 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI YODER, MERVIN C. · 1999 to 2008
$3.0M
Hematepoietic Stem Cell Transduction by AAV2 VectorsR01HL065570 · NHLBI · UNIVERSITY OF FLORIDA · PI SRIVASTAVA, ARUN · 2001 to 2004
$1.7M
PARVOVIRUS VECTORS FOR HUMAN GENE THERAPYR01HL058881 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI SRIVASTAVA, ARUN · 1997 to 2002
$1.2M
NHLBI NIH HHS HL 65570NHLBI NIH HHS R01 HL058881NHLBI NIH HHS R01 HL063169NHLBI NIH HHS R01 HL065570NHLBI NIH HHS R01 HL 58881NHLBI NIH HHS R01 HL 63169NHLBI NIH HHS T32 HL007910NHLBI NIH HHS T32 HL 07910
6 · The paper itself

Abstract

The use of adeno-associated virus type 2 (AAV) vectors has gained attention as a potentially useful alternative to the more commonly used retrovirus and adenovirus vectors for human gene therapy. However, the transduction efficiency of AAV vectors varies greatly in different cells and tissues in vitro and in vivo. We have documented that a cellular protein that binds the immunosuppressant drug FK506, termed the FK506-binding protein (FKBP52), interacts with the single-stranded D sequence within the AAV inverted terminal repeats, inhibits viral second-strand DNA synthesis, and consequently limits high-efficiency transgene expression (K. Qing, J. Hansen, K. A. Weigel-Kelley, M. Tan, S. Zhou, and A. Srivastava, J. Virol., 75: 8968-8976, 2001). FKBP52 can be phosphorylated at both tyrosine and serine/threonine residues, but only the phosphorylated forms of FKBP52 interact with the D sequence. Furthermore, the tyrosine-phosphorylated FKBP52 inhibits AAV second-strand DNA synthesis by greater than 90%, and the serine/threonine-phosphorylated FKBP52 causes approximately 40% inhibition, whereas the dephosphorylated FKBP52 has no effect on AAV second-strand DNA synthesis. In the present study, we have identified that the tyrosine-phosphorylated form of FKBP52 is a substrate for the cellular T-cell protein tyrosine phosphatase (TC-PTP). Deliberate overexpression of the murine wild-type (wt) TC-PTP gene, but not that of a cysteine-to-serine (C-S) mutant, caused tyrosine dephosphorylation of FKBP52, leading to efficient viral second-strand DNA synthesis and resulting in a significant increase in AAV-mediated transduction efficiency in HeLa cells in vitro. Both wt and C-S mutant TC-PTP expression cassettes were also used to generate transgenic mice. Primitive hematopoietic stem/progenitor cells from wt TC-PTP-transgenic mice, but not from C-S mutant TC-PTP-transgenic mice, could be successfully transduced by recombinant AAV vectors. These studies corroborate the fact that tyrosine phosphorylation of the cellular FKBP52 protein strongly influences AAV transduction efficiency, which may have important implications in the optimal use of AAV vectors in human gene therapy.

Indexed as

Genetic VectorsGene Transfer TechniquesMice, TransgenicTransgenesAnimalsDependovirusGenetic TherapyHeLa CellsHumansMicePhosphorylationProtein Tyrosine Phosphatase, Non-Receptor Type 2Protein Tyrosine PhosphatasesTacrolimus Binding ProteinsTransduction, GeneticTyrosineProtein Tyrosine Phosphatase, Non-Receptor Type 2Protein Tyrosine PhosphatasesPTPN2 protein, humanPtpn2 protein, mousetacrolimus binding protein 4Tacrolimus Binding ProteinsTyrosine

Identifiers

PMID12552015
PMCPMC141114
OpenAlexW2160411205

What OpenQuestion holds

Textmetadata
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.