Evidence map›Paper›PMID 19675127›Full record

ArticleDevelopment (Cambridge, England)2009

Systematic analysis of dynamic miRNA-target interactions during C. elegans development.

Liang Zhang, Molly Hammell, Brian A Kudlow, Victor Ambros, Min Han

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Short interspersed DNA elements and miRNAs: a novel hidden gene regulation layer in zebrafish?Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2015
    Article
  10. Article
  11. Article
  12. microRNAs of parasitic helminths - Identification, characterization and potential as drug targets.International journal for parasitology. Drugs and drug resistance · 2014
    Review
  13. Insights into miRNA regulation of the human glycome.Biochemical and biophysical research communications · 2014
    Article
  14. Mapping posttranscriptional regulation of the human glycome uncovers microRNA defining the glycocode.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

5 authors.

Liang ZhangHoward Hughes Medical Institute and Department of MCDB, University of Colorado, Boulder, CO 80309, USA.
Molly Hammell
Brian A Kudlow
Victor Ambros
Min Han

Funding

GENETIC CONTROL OF NEMATODE DEVELOPMENTR01GM034028 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI AMBROS, VICTOR · 1985 to 2018
$7.0M
Functional analysis of microRNA genes in DrosophilaR01GM066826 · NIGMS · DARTMOUTH COLLEGE · PI AMBROS, VICTOR · 2004 to 2007
$1.1M
Developmental Regulation of MicroRNA ExpressionR01GM088365 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI AMBROS, VICTOR · 2009 to 2010
$771k
A systematic analysis of mir-34 function in C. elegansF32GM087039 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI GALE HAMMELL, MOLLY · 2009 to 2010
$80k
Howard Hughes Medical InstituteNIGMS NIH HHS F32GM087039NIGMS NIH HHS GM066826NIGMS NIH HHS GM34028NIGMS NIH HHS GM47869NIGMS NIH HHS R01 GM088365
6 · The paper itself

Abstract

Although microRNA (miRNA)-mediated functions have been implicated in many aspects of animal development, the majority of miRNA::mRNA regulatory interactions remain to be characterized experimentally. We used an AIN/GW182 protein immunoprecipitation approach to systematically analyze miRNA::mRNA interactions during C. elegans development. We characterized the composition of miRNAs in functional miRNA-induced silencing complexes (miRISCs) at each developmental stage and identified three sets of miRNAs with distinct stage-specificity of function. We then identified thousands of miRNA targets in each developmental stage, including a significant portion that is subject to differential miRNA regulation during development. By identifying thousands of miRNA family-mRNA pairs with temporally correlated patterns of AIN-2 association, we gained valuable information on the principles of physiological miRNA::target recognition and predicted 1589 high-confidence miRNA family::mRNA interactions. Our data support the idea that miRNAs preferentially target genes involved in signaling processes and avoid genes with housekeeping functions, and that miRNAs orchestrate temporal developmental programs by coordinately targeting or avoiding genes involved in particular biological functions.

Indexed as

Caenorhabditis elegansGene Expression Regulation, Developmental3' Untranslated RegionsAnimalsCaenorhabditis elegans ProteinsCarrier ProteinsGene Expression ProfilingMicroRNAsOligonucleotide Array Sequence AnalysisRecombinant Fusion ProteinsRNA, Messenger3' Untranslated RegionsAIN-2 protein, C elegansCaenorhabditis elegans ProteinsCarrier ProteinsMicroRNAsRecombinant Fusion ProteinsRNA, Messenger

Identifiers

PMID19675127
PMCPMC2730362

What OpenQuestion holds

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Read underepoch 390

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.