Evidence map›Paper›PMID 26176784›Full record

ArticlePloS one2015

Expression and Misexpression of the miR-183 Family in the Developing Hearing Organ of the Chicken.

Kaidi D Zhang, Michelle L Stoller, Donna M Fekete

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Development (Cambridge, England) · 2020
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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 at 2 institutions in 1 country.

Kaidi D ZhangDepartment of Biological Sciences, Purdue University, West Lafayette, Indiana, United States of America.
Michelle L StollerDepartment of Biological Sciences, Purdue University, West Lafayette, Indiana, United States of America.
Donna M FeketeDepartment of Biological Sciences, Purdue University, West Lafayette, Indiana, United States of America; Purdue University Center for Cancer Research, Purdue University, West Lafayette, Indiana, United States of America.
Purdue University West Lafayette · USCenter for Cancer Research · US

Funding

Transgenic Mouse Core Facility Shared Resource (TMCF-SR)P30CA023168 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI Yoon Yeo · 1985 to 2026
$43.4M
DEVELOPMENT STUDIES OF THE INNER EARR01DC002756 · NIDCD · PURDUE UNIVERSITY WEST LAFAYETTE · PI FEKETE, DONNA M · 1995 to 2019
$6.8M
Gene Transfer Tools for Delivery and Investigation of Inner Ear MicroRNAsF31DC011687 · NIDCD · PURDUE UNIVERSITY · PI STOLLER, MICHELLE LYNN · 2011 to 2014
$124k
NCI NIH HHS P300CA023168NCI NIH HHS P30 CA023168NIDCD NIH HHS F31 DC011687NIDCD NIH HHS F31DC011687NIDCD NIH HHS R01 DC002756NIDCD NIH HHS R01DC002756
6 · The paper itself

Abstract

The miR-183 family consists of 3 related microRNAs (miR-183, miR-96, miR-182) that are required to complete maturation of primary sensory cells in the mammalian inner ear. Because the level of these microRNAs is not uniform across hair cell subtypes in the murine cochlea, the question arises as to whether hair cell phenotypes are influenced by microRNA expression levels. To address this, we used the chicken embryo to study expression and misexpression of this gene family. By in situ hybridization, expression of all 3 microRNAs is robust in immature hair cells of both auditory and vestibular organs and is present in the statoacoustic ganglion. The auditory organ, called the basilar papilla, shows a weak radial gradient (highest on the neural side) in prosensory cells near the base on embryonic day 7. About nine days later, the basilar papilla also displays a longitudinal gradient (highest in apical hair cells) for the 3 microRNAs. Tol2-mediated gene delivery was used to ask whether cell phenotypes are malleable when the prosensory epithelium was forced to overexpress the miR-183 family. The expression plasmid included EGFP as a reporter located upstream of an intron carrying the microRNA genes. The vectors were electroporated into the otic cup/vesicle, resulting in strong co-expression of EGFP and the miR-183 family that persisted for at least 2 weeks. This manipulation did not generate ectopic hair cells in non-sensory territories of the cochlear duct, although within the basilar papilla, hair cells were over-represented relative to supporting cells. There was no evidence for a change in hair cell phenotypes, such as short-to-tall, or basal-to-apical hair cell features. Therefore, while increasing expression of the miR-183 family was sufficient to influence cell lineage decisions, it did not redirect the differentiation of hair cells towards alternative radial or longitudinal phenotypes.

Indexed as

Gene ExpressionAnimalsAvian ProteinsCell DifferentiationChick EmbryoGene Expression Regulation, DevelopmentalHair Cells, AuditoryHEK293 CellsHumansMicroRNAsOrgan of CortiRNA InterferenceSpiral GanglionAvian ProteinsMicroRNAs

Identifiers

PMID26176784
PMCPMC4503353
OpenAlexW1548461771

What OpenQuestion holds

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LicenceCC BY
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.