Evidence map›Paper›PMID 20932845›Full record

ArticleJournal of molecular biology2010

Substrate-specific kinetics of Dicer-catalyzed RNA processing.

Srinivas Chakravarthy, Samuel H Sternberg, Colleen A Kellenberger, Jennifer A Doudna

Open access · bronzeAbstract read
In one paragraph

Article in Journal of molecular biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

94 citing papers in PubMed, 146 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
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  9. Article
  10. Nuclear miRNAs: Gene Regulation Activities.International journal of molecular sciences · 2024
    Review
  11. Article
  12. Next-Cell Hypothesis: Mechanism of Obesity-Associated Carcinogenesis.Advances in experimental medicine and biology · 2024
    Review
  13. MicroRNAs as Epigenetic Regulators of Obesity.Advances in experimental medicine and biology · 2024
    Review
  14. Regulatory role of RNA-binding proteins in microRNA biogenesis.Frontiers in molecular biosciences · 2024
    Review
  15. Structure of pre-miR-31 reveals an active role in Dicer-TRBP complex processing.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  16. Article
  17. Article
  18. Structural Modifications of siRNA Improve Its Performance In Vivo.International journal of molecular sciences · 2023
    Review
  19. Structure of pre-miR-31 reveals an active role in Dicer processing.bioRxiv : the preprint server for biology · 2023
    Article
  20. Review

34 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Srinivas ChakravarthyHoward Hughes Medical Institute, Berkeley, CA 94720, USA.
Samuel H Sternberg
Colleen A Kellenberger
Jennifer A Doudna
Howard Hughes Medical Institute · USUniversity of California, Berkeley · US

Funding

Structure and Function of RNAi-related NucleasesR01GM073794 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI DOUDNA, JENNIFER A · 2005 to 2013
$2.1M
NIGMS NIH HHS R01 GM073794
6 · The paper itself

Abstract

The specialized ribonuclease Dicer plays a central role in eukaryotic gene expression by producing small regulatory RNAs-microRNAs (miRNAs) and short interfering RNAs (siRNAs)-from larger double-stranded RNA (dsRNA) substrates. Although Dicer will cleave both imperfectly base-paired hairpin structures (pre-miRNAs) and perfect duplexes (pre-siRNAs) in vitro, it has not been clear whether these are mechanistically equivalent substrates and how dsRNA binding proteins such as trans-activation response (TAR) RNA binding protein (TRBP) influence substrate selection and RNA processing efficiency. We show here that human Dicer is much faster at processing a pre-miRNA substrate compared to a pre-siRNA substrate under both single and multiple turnover conditions. Maximal cleavage rates (V(max)) calculated by Michaelis-Menten analysis differed by more than 100-fold under multiple turnover conditions. TRBP was found to enhance dicing of both substrates to similar extents, and this stimulation required the two N-terminal dsRNA binding domains of TRBP. These results demonstrate that multiple factors influence dicing kinetics. While TRBP stimulates dicing by enhancing the stability of Dicer-substrate complexes, Dicer itself generates product RNAs at rates determined at least in part by the structural properties of the substrate.

Indexed as

RNA Processing, Post-TranscriptionalAmino Acid SubstitutionBase SequenceDEAD-box RNA HelicasesHumansIn Vitro TechniquesKineticsMicroRNAsModels, BiologicalMutagenesis, Site-DirectedPhosphorylationProtein Interaction Domains and MotifsRecombinant ProteinsRibonuclease IIIRNA-Binding ProteinsRNA PrecursorsDEAD-box RNA HelicasesDICER1 protein, humanMicroRNAsmirnlet7 microRNA, humanRecombinant ProteinsRibonuclease IIIRNA-Binding ProteinsRNA PrecursorsTrans-Activation Responsive RNA-Binding Protein

Identifiers

PMID20932845
PMCPMC3005596
OpenAlexW2093928169

What OpenQuestion holds

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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.