Evidence map›Paper›PMID 21158564›Full record

ArticleZebrafish2010

A zebrafish cell culture assay for the identification of microRNA targets.

Weiyi Liu, Yihong Guan, Paul Collodi

Abstract read
In one paragraph

Article in Zebrafish, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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.

Weiyi LiuDepartment of Animal Sciences, Purdue University, West Lafayette, Indiana 47907, USA.
Yihong Guan
Paul Collodi

Funding

Zebrafish ES cell lines for targeted mutagenesisR01GM069384 · NIGMS · PURDUE UNIVERSITY WEST LAFAYETTE · PI COLLODI, PAUL · 2003 to 2010
$2.6M
NIGMS NIH HHS R01 GM069384NIGMS NIH HHS R01GM069384
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are endogenous small noncoding RNAs that regulate gene expression at the posttranscriptional level. Studies have shown that zebrafish miRNAs play a key role in embryo development, tissue fate establishment, and differentiation by interacting with specific targets, usually in the 3'UTR of the mRNA. Identification of the target sequence is fundamental to elucidating miRNA function. Since bioinformatics can predict hundreds of potential targets for each miRNA, experimental validation of the actual target site is required. Although recent studies have employed the HEK293 cell line to investigate mammalian miRNA targets, our results have shown that the cell line is not suitable for studies of zebrafish miR-430b miRNA. In this article we describe a convenient in vitro assay system that involves the use of zebrafish cell cultures and a luciferase reporter construct to evaluate miR-430b target sites. The cell culture-based assay could be used to validate target sequences of other zebrafish miRNAs.

Indexed as

Genetic TechniquesZebrafishAnimalsCell Culture TechniquesCell LineDNA, ComplementaryMicroRNAsRNA, MessengerDNA, ComplementaryMicroRNAsRNA, Messenger

Identifiers

PMID21158564
PMCPMC3017427

What OpenQuestion holds

Textmetadata
LicenceTDM
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.