Evidence map›Paper›PMID 27815363›Full record

ArticleGenetics2017

Stage-Specific Timing of the microRNA Regulation of lin-28 by the Heterochronic Gene lin-14 in Caenorhabditis elegans.

Jennifer Tsialikas, Mitchell A Romens, Allison Abbott, Eric G Moss

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. A molecular timer couples organism-wide temporal identity to developmental checkpoints.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. A developmental timer coordinates organism-wide microRNA transcription.bioRxiv : the preprint server for biology · 2026
    Article
  4. From nematode to Nobel: How community-shared resources fueled the rise ofProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. The multifaceted roles of microRNAs in differentiation.Current opinion in cell biology · 2020
    Review
  11. Development (Cambridge, England) · 2019
    Article
  12. Regulation of nuclear-cytoplasmic partitioning by theDevelopment (Cambridge, England) · 2019
    Article
  13. Article
  14. Article
  15. 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

4 authors at 2 institutions in 1 country.

Jennifer TsialikasDepartment of Molecular Biology, Rowan University, Stratford, New Jersey 08084.
Mitchell A RomensDepartment of Biological Sciences, Marquette University, Milwaukee, Wisconsin 53233.
Allison AbbottDepartment of Biological Sciences, Marquette University, Milwaukee, Wisconsin 53233.
Eric G MossDepartment of Molecular Biology, Rowan University, Stratford, New Jersey 08084 mosseg@rowan.edu.ORCID 0000-0002-0113-6618
Marquette University · USRowan University · US

Funding

Genetic Analysis of Conserved microRNAs in C. elegansR15GM084451 · NIGMS · MARQUETTE UNIVERSITY · PI ABBOTT, ALLISON LYNN · 2008 to 2014
$868k
NIGMS NIH HHS R15 GM084451
6 · The paper itself

Abstract

In normal development, the order and synchrony of diverse developmental events must be explicitly controlled. In the nematode Caenorhabditis elegans, the timing of larval events is regulated by hierarchy of proteins and microRNAs (miRNAs) known as the heterochronic pathway. These regulators are organized in feedforward and feedback interactions to form a robust mechanism for specifying the timing and execution of cell fates at successive stages. One member of this pathway is the RNA binding protein LIN-28, which promotes pluripotency and cell fate decisions in successive stages. Two genetic circuits control LIN-28 abundance: it is negatively regulated by the miRNA lin-4, and positively regulated by the transcription factor LIN-14 through a mechanism that was previously unknown. In this report, we used animals that lack lin-4 to elucidate LIN-14's activity in this circuit. We demonstrate that three let-7 family miRNAs-miR-48, miR-84, and miR-241-inhibit lin-28 expression. Furthermore, we show genetically that these miRNAs act between lin-14 and lin-28, and that they comprise the pathway by which lin-14 positively regulates lin-28 We also show that the lin-4 family member mir-237, also regulates early cell fates. Finally, we show that the expression of these miRNAs is directly inhibited by lin-14 activity, making them the first known targets of lin-14 that act in the heterochronic pathway.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell DifferentiationGene Expression Regulation, DevelopmentalLarvaMicroRNAsNuclear ProteinsRepressor ProteinsRNA-Binding ProteinsTranscription FactorsCaenorhabditis elegans Proteinslet-7 microRNA, C elegansLIN-14 protein, C elegansLIN-28 protein, C eleganslin-4 microRNA, C elegansMicroRNAsNuclear ProteinsRepressor ProteinsRNA-Binding ProteinsTranscription FactorsC. elegansheterochronic geneslet-7LIN-14LIN-28microRNA

Identifiers

PMID27815363
PMCPMC5223506
OpenAlexW2548590503

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.