Evidence map›Paper›PMID 38230563›Full record

ArticleDevelopment (Cambridge, England)2024

Seven-up acts in neuroblasts to specify adult central complex neuron identity and initiate neuroblast decommissioning.

Noah R Dillon, Laurina Manning, Keiko Hirono, Chris Q Doe

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Cell cycle-dependent cues regulate temporal patterning of thebioRxiv : the preprint server for biology · 2025
    Article
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Noah R DillonInstitute of Neuroscience, Howard Hughes Medical Institute, University of Oregon, Eugene, OR 97403, USA.ORCID 0000-0002-6708-4208
Laurina ManningInstitute of Neuroscience, Howard Hughes Medical Institute, University of Oregon, Eugene, OR 97403, USA.ORCID 0000-0003-3730-3702
Keiko HironoInstitute of Neuroscience, Howard Hughes Medical Institute, University of Oregon, Eugene, OR 97403, USA.ORCID 0009-0005-5489-2790
Chris Q DoeInstitute of Neuroscience, Howard Hughes Medical Institute, University of Oregon, Eugene, OR 97403, USA.ORCID 0000-0001-5980-8029
Howard Hughes Medical Institute · US

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
DEVELOPMENTAL BIOLOGY TRAINING PROGRAMT32HD007348 · NICHD · UNIVERSITY OF OREGON · PI Chris Q Doe, KRYN STANKUNAS · 1989 to 2026
$6.8M
GENETIC AND MOLECULAR STUDIES OF NEUROGENESISR01HD027056 · NICHD · UNIVERSITY OF OREGON · PI Chris Q Doe · 1989 to 2026
$5.0M
Genetic and Molecular Studies of NeurogenesisR37HD027056 · NICHD · UNIVERSITY OF OREGON · PI DOE, CHRIS Q · 2012 to 2021
$3.0M
Howard Hughes Medical InstituteHoward Hughes Medical Institute n/aNICHD NIH HHS R01 HD027056NICHD NIH HHS R37 HD027056NICHD NIH HHS T32 HD007348NIH HHS HD27056NIH HHS P40 OD018537
6 · The paper itself

Abstract

An unanswered question in neurobiology is how are diverse neuron cell types generated from a small number of neural stem cells? In the Drosophila larval central brain, there are eight bilateral Type 2 neuroblast (T2NB) lineages that express a suite of early temporal factors followed by a different set of late temporal factors and generate the majority of the central complex (CX) neurons. The early-to-late switch is triggered by the orphan nuclear hormone receptor Seven-up (Svp), yet little is known about how this Svp-dependent switch is involved in specifying CX neuron identities. Here, we: (1) birth date the CX neurons P-EN and P-FN (early and late, respectively); (2) show that Svp is transiently expressed in all early T2NBs; and (3) show that loss of Svp expands the population of early born P-EN neurons at the expense of late born P-FN neurons. Furthermore, in the absence of Svp, T2NBs fail decommissioning and abnormally extend their lineage into week-old adults. We conclude that Svp is required to specify CX neuron identity, as well as to initiate T2NB decommissioning.

Indexed as

Drosophila ProteinsNeural Stem CellsAnimalsCell LineageDNA-Binding ProteinsDrosophilaDrosophila melanogasterNeuronsTranscription FactorsDNA-Binding ProteinsDrosophila ProteinsTranscription FactorsCentral complexDrosophilaSeven-upTemporal specification

Identifiers

PMID38230563
PMCPMC10906098
OpenAlexW4390949109

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.