Evidence map›Paper›PMID 34100067›Full record

ArticleDevelopment (Cambridge, England)2021

Piecemeal regulation of convergent neuronal lineages by bHLH transcription factors in Caenorhabditis elegans.

Neda Masoudi, Eviatar Yemini, Ralf Schnabel, Oliver Hobert

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Article
  2. Regulation of motor neuron differentiation in thebioRxiv : the preprint server for biology · 2025
    Article
  3. A gene expression atlas of a juvenile nervous system.bioRxiv : the preprint server for biology · 2025
    Article
  4. Single-cell transcriptomic profiling ofbioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Functional analysis of conservedbioRxiv : the preprint server for biology · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Transcriptional regulation of neuronal identity.The European journal of neuroscience · 2022
    Review
  16. Review
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.

Neda MasoudiDepartment of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, NY 10027, USA.
Eviatar YeminiDepartment of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, NY 10027, USA.ORCID 0000-0003-1977-0761
Ralf SchnabelInstitute of Genetics, Technische Universität Braunschweig, 38106 Braunschweig, Germany.
Oliver HobertDepartment of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, NY 10027, USA.ORCID 0000-0002-7634-2854

Funding

Hormones: Molecular Mechanism of Action and FunctionsT32DK007328 · NIDDK · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI KOUSTENI, STAVROULA · 1986 to 2025
$7.8M
NIDDK NIH HHS T32 DK007328
6 · The paper itself

Abstract

Cells of the same type can be generated by distinct cellular lineages that originate in different parts of the developing embryo ('lineage convergence'). Several Caenorhabditis elegans neuron classes composed of left/right or radially symmetric class members display such lineage convergence. We show here that the C. elegans Atonal homolog lin-32 is differentially expressed in neuronal lineages that give rise to left/right or radially symmetric class members. Loss of lin-32 results in the selective loss of the expression of pan-neuronal markers and terminal selector-type transcription factors that confer neuron class-specific features. Another basic helix-loop-helix (bHLH) gene, the Achaete-Scute homolog hlh-14, is expressed in a mirror image pattern relative to lin-32 and is required to induce neuronal identity and terminal selector expression on the contralateral side of the animal. These findings demonstrate that distinct lineage histories converge via different bHLH factors at the level of induction of terminal selector identity determinants, which thus serve as integrators of distinct lineage histories. We also describe neuron-to-neuron identity transformations in lin-32 mutants, which we propose to also be the result of misregulation of terminal selector gene expression.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell DifferentiationCell LineageEmbryo, NonmammalianGene Expression Regulation, DevelopmentalNeuronsTranscription FactorsBasic Helix-Loop-Helix ProteinsCaenorhabditis elegans ProteinsHLH-14 protein, C elegansLIN-32 protein, C elegansTranscription FactorsC. elegansLineageNeuronal differentiationTranscriptional control

Identifiers

PMID34100067
PMCPMC8217713

What Socratic holds

Textmetadata
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 Socratic graph.