Evidence map›Paper›PMID 19805217›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

Identification of an RNA-dependent RNA polymerase in Drosophila involved in RNAi and transposon suppression.

Concetta Lipardi, Bruce M Paterson

RetractedOpen access · greenAbstract readRetracted Publication
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
6.7field-weighted citation impact, top 2% 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

38 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. RNAi technology: a new platform for crop pest control.Physiology and molecular biology of plants : an international journal of functional plant biology · 2017
    Review
  6. Predicted trans-acting siRNAs in the human brain.International journal of molecular sciences · 2015
    Article
  7. Review
  8. Article
  9. Tick cell lines for study of Crimean-Congo hemorrhagic fever virus and other arboviruses.Vector borne and zoonotic diseases (Larchmont, N.Y.) · 2012
    Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. RNA interference and heterochromatin assembly.Cold Spring Harbor perspectives in biology · 2011
    Review
  17. Review
  18. Article
  19. Article
  20. RNAi effector diversity in nematodes.PLoS neglected tropical diseases · 2011
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Concetta LipardiLaboratory of Biochemistry and Molecular Biology, National Cancer Institute, National Institutes of Health, Building 37, Room 6118, 9000 Rockville Pike, Bethesda, MD 20892, USA.
Bruce M Paterson
National Institutes of Health · US

Funding

Molecular Studies of Eukaryotic Gene RegulationZIABC005258 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI PATERSON, BRUCE · 2009 to 2015
$6.1M
6 · The paper itself

Abstract

Here, we show that recombinant Drosophila elp1 (D-elp1) produced in Sf9 cells or Escherichia coli, corresponding to the largest of the three subunits in the RNA polymerase II core elongator complex, has RNA-dependent RNA polymerase (RdRP) activity. D-elp1 is a noncanonical RdRP that can synthesize dsRNA from different ssRNA templates using either a primer-dependent or primer-independent initiation mechanism. Of the three core subunits, only D-elp1 depletion inhibits RNAi in S2 cells but does not affect micro RNA function. Furthermore, D-elp1 depletion results in increased steady state levels of representative transposon RNAs and a decrease in the corresponding transposon antisense transcripts and endo siRNAs. In contrast, although Dcr-2 depletion results in increased transposon RNA levels and a reduction in the corresponding endo siRNAs, there is no change in the transposon antisense RNA levels. In D-elp1 null third instar larvae transposon RNA levels are also increased and the corresponding transposon antisense RNAs are reduced. D-elp1 associates tightly with Dcr-2, similar to the Dicer-RdRP interaction observed in lower eukaryotes. These results identify an aspect of the RNAi pathway in Drosophila that suggest transposon derived endo siRNAs, critical for transposon suppression, are produced, in part, in a D-elp1 dependent step that converts transposon RNA into dsRNA that is subsequently processed by Dcr-2. The generality of this mechanism in genome defense and RNA silencing in higher eukaryotes is suggested.

Indexed as

AnimalsBaculoviridaeCell LineDNA Transposable ElementsDrosophilaDrosophila ProteinsEscherichia coliGene DeletionGenes, InsectRecombinant ProteinsRibonuclease IIIRNA-Dependent RNA PolymeraseRNA HelicasesRNA InterferenceSuppression, GeneticDCR-2 protein, DrosophilaDNA Transposable ElementsDrosophila ProteinsRecombinant ProteinsRibonuclease IIIRNA-Dependent RNA PolymeraseRNA Helicases

Identifiers

PMID19805217
PMCPMC2736140
OpenAlexW2162674498

What OpenQuestion holds

Textmetadata
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.