Evidence map›Paper›PMID 18302773›Full record

ArticleBMC developmental biology2008

Hey2 functions in parallel with Hes1 and Hes5 for mammalian auditory sensory organ development.

Shuangding Li, Sharayne Mark, Kristen Radde-Gallwitz, Rebecca Schlisner, Michael T Chin, Ping Chen

Open access · hybridAbstract read
In one paragraph

Article in BMC developmental biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

44 citing papers in PubMed, 78 citations in OpenAlex.

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  8. The Notch Ligand Jagged1 Is Required for the Formation, Maintenance, and Survival of Hensen's Cells in the Mouse Cochlea.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
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  10. The acquisition of positional information across the radial axis of the cochlea.Developmental dynamics : an official publication of the American Association of Anatomists · 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

6 authors at 2 institutions in 1 country.

Shuangding LiDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322, USA. sli24@emory.edu
Sharayne Mark
Kristen Radde-Gallwitz
Rebecca Schlisner
Michael T Chin
Ping Chen
Emory University · USUniversity of Washington · US

Funding

Morphogenesis of the Organ of CortiR01DC005213 · NIDCD · HOUSE EAR INSTITUTE · PI CHEN, PING · 2002 to 2014
$3.3M
NIDCD NIH HHS R01 DC005213
6 · The paper itself

Abstract

backgroundDuring mouse development, the precursor cells that give rise to the auditory sensory organ, the organ of Corti, are specified prior to embryonic day 14.5 (E14.5). Subsequently, the sensory domain is patterned precisely into one row of inner and three rows of outer sensory hair cells interdigitated with supporting cells. Both the restriction of the sensory domain and the patterning of the sensory mosaic of the organ of Corti involve Notch-mediated lateral inhibition and cellular rearrangement characteristic of convergent extension. This study explores the expression and function of a putative Notch target gene.

resultsWe report that a putative Notch target gene, hairy-related basic helix-loop-helix (bHLH) transcriptional factor Hey2, is expressed in the cochlear epithelium prior to terminal differentiation. Its expression is subsequently restricted to supporting cells, overlapping with the expression domains of two known Notch target genes, Hairy and enhancer of split homolog genes Hes1 and Hes5. In combination with the loss of Hes1 or Hes5, genetic inactivation of Hey2 leads to increased numbers of mis-patterned inner or outer hair cells, respectively. Surprisingly, the ectopic hair cells in Hey2 mutants are accompanied by ectopic supporting cells. Furthermore, Hey2-/-;Hes1-/- and Hey2-/-;Hes1+/- mutants show a complete penetrance of early embryonic lethality.

conclusionOur results indicate that Hey2 functions in parallel with Hes1 and Hes5 in patterning the organ of Corti, and interacts genetically with Hes1 for early embryonic development and survival. Our data implicates expansion of the progenitor pool and/or the boundaries of the developing sensory organ to account for patterning defects observed in Hey2 mutants.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsBody PatterningCell CountEmbryo, MammalianGene Expression Regulation, DevelopmentalHomeodomain ProteinsImmunohistochemistryIn Situ HybridizationMiceMice, Inbred C57BLMice, Mutant StrainsOrgan of CortiOrganogenesisPolymerase Chain ReactionRepressor ProteinsBasic Helix-Loop-Helix ProteinsHes1 protein, mouseHes5 protein, mouseHey2 protein, mouseHomeodomain ProteinsRepressor ProteinsTranscription Factor HES-1

Identifiers

PMID18302773
PMCPMC2277407
OpenAlexW2084008439

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.