Evidence map›Paper›PMID 29324767›Full record

ArticlePLoS genetics2018

Glass promotes the differentiation of neuronal and non-neuronal cell types in the Drosophila eye.

Carolyn A Morrison, Hao Chen, Tiffany Cook, Stuart Brown, Jessica E Treisman

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 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, 20 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Carolyn A MorrisonSkirball Institute for Biomolecular Medicine and Department of Cell Biology, NYU School of Medicine, New York, NY, United States of America.
Hao ChenDepartment of Cell Biology, NYU School of Medicine, New York, NY, United States of America.
Tiffany CookCenter of Molecular Medicine and Genomics and Department of Ophthalmology, Wayne State University School of Medicine, Detroit, MI, United States of America.
Stuart BrownDepartment of Cell Biology, NYU School of Medicine, New York, NY, United States of America.
Jessica E TreismanSkirball Institute for Biomolecular Medicine and Department of Cell Biology, NYU School of Medicine, New York, NY, United States of America.ORCID 0000-0002-7453-107X
New York University · USWayne State University · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Pattern formation in the eye discR01EY013777 · NEI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI TREISMAN, JESSICA E · 2002 to 2017
$5.8M
Photoreceptor cell fate specification by the Glass transcription factorR21EY024826 · NEI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI TREISMAN, JESSICA E · 2014 to 2015
$461k
Defining Glial Programs that Support Adult Photoreceptor Form and FunctionR21EY024405 · NEI · WAYNE STATE UNIVERSITY · PI COOK, TIFFANY · 2014 to 2015
$425k
Identifying the transcriptional core logic that determines photoreceptor cell specificationF31EY025129 · NEI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MORRISON, CAROLYN ARLENE · 2015 to 2017
$119k
NCI NIH HHS P30 CA016087NEI NIH HHS F31 EY025129NEI NIH HHS R01 EY013777NEI NIH HHS R21 EY024405NEI NIH HHS R21 EY024826NIH HHS F31-EY025129NIH HHS P30-CA016087
6 · The paper itself

Abstract

Transcriptional regulators can specify different cell types from a pool of equivalent progenitors by activating distinct developmental programs. The Glass transcription factor is expressed in all progenitors in the developing Drosophila eye, and is maintained in both neuronal and non-neuronal cell types. Glass is required for neuronal progenitors to differentiate as photoreceptors, but its role in non-neuronal cone and pigment cells is unknown. To determine whether Glass activity is limited to neuronal lineages, we compared the effects of misexpressing it in neuroblasts of the larval brain and in epithelial cells of the wing disc. Glass activated overlapping but distinct sets of genes in these neuronal and non-neuronal contexts, including markers of photoreceptors, cone cells and pigment cells. Coexpression of other transcription factors such as Pax2, Eyes absent, Lozenge and Escargot enabled Glass to induce additional genes characteristic of the non-neuronal cell types. Cell type-specific glass mutations generated in cone or pigment cells using somatic CRISPR revealed autonomous developmental defects, and expressing Glass specifically in these cells partially rescued glass mutant phenotypes. These results indicate that Glass is a determinant of organ identity that acts in both neuronal and non-neuronal cells to promote their differentiation into functional components of the eye.

Indexed as

Drosophila melanogasterAnimalsAnimals, Genetically ModifiedCell DifferentiationDNA-Binding ProteinsDrosophila ProteinsEmbryo, NonmammalianEyeFemaleGene Expression Regulation, DevelopmentalNeural Stem CellsOrganogenesisStem CellsDNA-Binding ProteinsDrosophila Proteinsgl protein, Drosophila

Identifiers

PMID29324767
PMCPMC5783423
OpenAlexW2783665659

What OpenQuestion holds

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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.