Evidence map›Paper›PMID 17426139›Full record

ArticleNucleic acids research2007

Optimization and characterization of tRNA-shRNA expression constructs.

Lisa J Scherer, Richard Frank, John J Rossi

Abstract read
In one paragraph

Article in Nucleic acids research, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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

29 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Novel RNA-based strategies for therapeutic gene silencing.Molecular therapy : the journal of the American Society of Gene Therapy · 2010
    Review
  18. Article
  19. Article
  20. Concepts in in vivo siRNA delivery for cancer therapy.Journal of cellular physiology · 2009
    Review
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

3 authors.

Lisa J SchererDepartment of Molecular Biology Beckman Research Institute of the City of Hope, 1450 E. Duarte Road, Duarte, California 91010, USA.
Richard Frank
John J Rossi

Funding

COMBINATORIAL USE OF CCR5 RIBOZYMES WITH ANTI HIV1 RNASR01AI042552 · NIAID · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI ROSSI, JOHN JOSEPH · 1998 to 2019
$7.8M
Enhancing the Intracellular Functioning of HIV RibozymesR37AI029329 · NIAID · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI ROSSI, JOHN JOSEPH · 2002 to 2011
$6.7M
Studies on RNAi Based Delivery in VivoR01DK078424 · NIDDK · STANFORD UNIVERSITY · PI KAY, MARK A · 2006 to 2014
$4.1M
YEAST SYSTEM FOR DEVELOPING ANTI-HIV-1 RIBOZYMESR01AI029329 · NIAID · LOMA LINDA UNIVERSITY · PI ROSSI, JOHN JOSEPH · 1990 to 2018
$3.9M
SELECTED TOPICS IN CARDIOLOGYT32HL007470 · NHLBI · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI GETTES, LEONARD S · 1985 to 1989
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NHLBI NIH HHS HL07470NIAID NIH HHS AI29329NIAID NIH HHS AI42552NIAID NIH HHS R01 AI029329NIAID NIH HHS R01 AI042552NIAID NIH HHS R37 AI029329NIDDK NIH HHS R01 DK078424
6 · The paper itself

Abstract

Expression of short hairpin RNAs via the use of PolIII-based transcription systems has proven to be an effective mechanism for triggering RNAi in mammalian cells. The most popular promoters for this purpose are the U6 and H1 promoters since they are easily manipulated for expression of shRNAs with defined start and stop signals. Multiplexing (the use of siRNAs against multiple targets) is one strategy that is being developed by a number of laboratories for the treatment of HIV infection since it increases the likelihood of suppressing the emergence of resistant virus in applications. In this context, the development of alternative small PolIII promoters other than U6 and H1 would be useful. We describe tRNA(Lys3)-shRNA chimeric expression cassettes which produce siRNAs with comparable efficacy and strand selectivity to U6-expressed shRNAs, and show that their activity is consistent with processing by endogenous 3' tRNAse. In addition, our observations suggest general guidelines for expressing effective tRNA-shRNAs with the potential for graded response, to minimize toxicities associated with competition for components of the endogenous RNAi pathway in cells.

Indexed as

RNA InterferenceBase SequenceCell LineGene Products, revGene Products, tatGenetic VectorsHIV-1HumansMolecular Sequence DataPromoter Regions, Geneticrev Gene Products, Human Immunodeficiency VirusRNA, Small InterferingRNA, Transfer, Amino AcylRNA, Untranslatedtat Gene Products, Human Immunodeficiency VirusGene Products, revGene Products, tatrev Gene Products, Human Immunodeficiency VirusRNA, Small InterferingRNA, Transfer, Amino AcylRNA, Untranslatedtat Gene Products, Human Immunodeficiency Virus

Identifiers

PMID17426139
PMCPMC1885648

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.