Evidence map›Paper›PMID 34887421›Full record

ArticleNature communications2021

Cell-type-specific chromatin occupancy by the pioneer factor Zelda drives key developmental transitions in Drosophila.

Elizabeth D Larson, Hideyuki Komori, Tyler J Gibson, Cyrina M Ostgaard, Danielle C Hamm, Jack M Schnell, Cheng-Yu Lee, Melissa M Harrison

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

32 citing papers in PubMed, 41 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

8 authors at 3 institutions in 1 country.

Elizabeth D Larson *Department of Biomolecular Chemistry, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Hideyuki Komori *Life Sciences Institute, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0001-9764-5654
Tyler J GibsonDepartment of Biomolecular Chemistry, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Cyrina M OstgaardDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.
Danielle C HammDepartment of Biomolecular Chemistry, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.ORCID http://orcid.org/0000-0003-2966-7389
Jack M SchnellDepartment of Biomolecular Chemistry, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Cheng-Yu LeeDivision of Genetic Medicine, Department of Internal Medicine and Comprehensive Cancer Center, University of Michigan Medical School, Ann Arbor, MI, USA. leecheng@umich.edu.ORCID http://orcid.org/0000-0003-2291-1297
Melissa M HarrisonDepartment of Biomolecular Chemistry, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA. mharrison3@wisc.edu.ORCID http://orcid.org/0000-0002-8228-6836
University of Wisconsin–Madison · USUniversity of Michigan · USUniversity of Southern California · US

Funding

Genomic reprogramming in the early embryoR35GM136298 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Melissa Harrison · 2020 to 2026
$2.8M
Shared mechanisms regulate transcription-factor activity to control cell fate in neural stem cells and the embryoR01NS111647 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI HARRISON, MELISSA, LEE, CHENG-YU · 2019 to 2023
$1.7M
Multi-layered Control of the Exit from StemnessR01NS107496 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEE, CHENG-YU · 2019 to 2023
$1.7M
NIGMS NIH HHS R35 GM136298NINDS NIH HHS R01 NS107496NINDS NIH HHS R01 NS111647
6 · The paper itself

Abstract

During Drosophila embryogenesis, the essential pioneer factor Zelda defines hundreds of cis-regulatory regions and in doing so reprograms the zygotic transcriptome. While Zelda is essential later in development, it is unclear how the ability of Zelda to define cis-regulatory regions is shaped by cell-type-specific chromatin architecture. Asymmetric division of neural stem cells (neuroblasts) in the fly brain provide an excellent paradigm for investigating the cell-type-specific functions of this pioneer factor. We show that Zelda synergistically functions with Notch to maintain neuroblasts in an undifferentiated state. Zelda misexpression reprograms progenitor cells to neuroblasts, but this capacity is limited by transcriptional repressors critical for progenitor commitment. Zelda genomic occupancy in neuroblasts is reorganized as compared to the embryo, and this reorganization is correlated with differences in chromatin accessibility and cofactor availability. We propose that Zelda regulates essential transitions in the neuroblasts and embryo through a shared gene-regulatory network driven by cell-type-specific enhancers.

Indexed as

AnimalsCell DifferentiationChromatinDrosophila melanogasterDrosophila ProteinsEmbryonic DevelopmentGene Expression Regulation, DevelopmentalNuclear ProteinsReceptors, NotchStem CellsChromatinDrosophila ProteinsN protein, DrosophilaNuclear ProteinsReceptors, Notchzld protein, Drosophila

Identifiers

PMID34887421
PMCPMC8660810
OpenAlexW4225647574

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.