Evidence map›Paper›PMID 28675662›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2018

Separate and coincident expression of Hes1 and Hes5 in the developing mouse eye.

Amy N Riesenberg, Kevin W Conley, Tien T Le, Nadean L Brown

Open access · bronzeAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Retinal regeneration requires dynamic Notch signaling.Neural regeneration research · 2022
    Review
  6. Article
  7. Review
  8. Article
  9. Simultaneous Requirements forThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  10. Article
  11. Notch Suppression Collaborates with Ascl1 and Lin28 to Unleash a Regenerative Response in Fish Retina, But Not in Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  12. Review
  13. 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 1 institution in 1 country.

Amy N RiesenbergDivision of Developmental Biology, Cincinnati Children's Hospital Research Foundation, Cincinnati, Ohio.
Kevin W ConleyDivision of Developmental Biology, Cincinnati Children's Hospital Research Foundation, Cincinnati, Ohio.
Tien T LeDivision of Developmental Biology, Cincinnati Children's Hospital Research Foundation, Cincinnati, Ohio.
Nadean L BrownDivision of Developmental Biology, Cincinnati Children's Hospital Research Foundation, Cincinnati, Ohio.ORCID 0000-0002-4906-4625
Cincinnati Children's Hospital Medical Center · US

Funding

The Mutant Mouse Resource and Research Center at the University of Missouri - ResourceU42OD010918 · OD · UNIVERSITY OF MISSOURI-COLUMBIA · PI Bret Daniel Ulery · 2012 to 2026
$25.1M
INVESTIGATION OF MAMMALIAN RETINAL NEURON DEVELOPMENTR01EY013612 · NEI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BROWN, NADEAN L · 2001 to 2020
$6.0M
Cell-Cell Signaling During Mammalian Early Eye FormationR01EY018097 · NEI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BROWN, NADEAN L · 2008 to 2016
$2.6M
NEI NIH HHS R01 EY013612NEI NIH HHS R01 EY018097NIH HHS U42 OD010918
6 · The paper itself

Abstract

backgroundNotch signaling is broadly required during embryogenesis, frequently activating the transcription of two basic helix-loop-helix transcription factors, Hes1 and Hes5. But, it remains unresolved when and where Hes1 and Hes5 act alone or together during development. Here, we analyzed a Hes5-green fluorescent protein (GFP) bacterial artificial chromosome (BAC) transgenic mouse, as a proxy for endogenous Hes5. We directly compared transgenic GFP expression with Hes1, and particular markers of embryonic lens and retina development.

resultsHes5-GFP is dynamic within subsets of retinal and lens progenitor cells, and differentiating retinal ganglion neurons, in contrast to Hes1 found in all progenitor cells. In the adult retina, only Müller glia express Hes5-GFP. Finally, Hes5-GFP is up-regulated in Hes1 germline mutants, consistent with previous demonstration that Hes1 suppresses Hes5 transcription.

conclusionsHes5-GFP BAC transgenic mice are useful for identifying Hes5-expressing cells. Although Hes5-GFP and Hes1 are coexpressed in particular developmental contexts, we also noted cohorts of lens or retinal cells expressing just one factor. The dynamic Hes5-GFP expression pattern, coupled with its derepressed expression in Hes1 mutants, suggests that this transgene contains the relevant cis-regulatory elements that regulate endogenous Hes5 in the mouse lens and retina. Developmental Dynamics 247:212-221, 2018. © 2017 Wiley Periodicals, Inc.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsGene Expression Regulation, DevelopmentalLens, CrystallineMiceMice, TransgenicOrganogenesisRepressor ProteinsRetinaSignal TransductionTranscription Factor HES-1Basic Helix-Loop-Helix ProteinsHes1 protein, mouseHes5 protein, mouseRepressor ProteinsTranscription Factor HES-1Hes1Hes5lens developmentNotch signalingretina, neurogenesis

Identifiers

PMID28675662
PMCPMC5739946
OpenAlexW2727474554

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.