Evidence map›Paper›PMID 28065609›Full record

ArticleCurrent biology : CB2017

Sexually Dimorphic Differentiation of a C. elegans Hub Neuron Is Cell Autonomously Controlled by a Conserved Transcription Factor.

Esther Serrano-Saiz, Meital Oren-Suissa, Emily A Bayer, Oliver Hobert

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

49 citing papers in PubMed, 97 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Morphologically defined substages of tail morphogenesis in C. elegans males.Developmental dynamics : an official publication of the American Association of Anatomists · 2024
    Review
  9. Article
  10. Review
  11. Article
  12. A neurotransmitter atlas ofbioRxiv : the preprint server for biology · 2024
    Article
  13. Morphologically defined substages of tail morphogenesis inbioRxiv : the preprint server for biology · 2024
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. PNAS nexus · 2022
    Article
  20. 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.

Esther Serrano-SaizDepartment of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, NY 10027, USA. Electronic address: es2754@columbia.edu.
Meital Oren-SuissaDepartment of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, NY 10027, USA.
Emily A BayerDepartment of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, NY 10027, USA.
Oliver HobertDepartment of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, NY 10027, USA. Electronic address: or38@columbia.edu.
Howard Hughes Medical Institute · US

Funding

Sexually dimorphic regulation of neuronal identity in C.elegansR37NS039996 · NINDS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI HOBERT, OLIVER · 2015 to 2021
$2.5M
Control of sexually dimorphic synaptic wiringF31NS096863 · NINDS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI BAYER, EMILY A · 2016 to 2018
$132k
NINDS NIH HHS F31 NS096863NINDS NIH HHS R37 NS039996
6 · The paper itself

Abstract

Functional and anatomical sexual dimorphisms in the brain are either the result of cells that are generated only in one sex or a manifestation of sex-specific differentiation of neurons present in both sexes. The PHC neuron pair of the nematode C. elegans differentiates in a strikingly sex-specific manner. In hermaphrodites the PHC neurons display a canonical pattern of synaptic connectivity similar to that of other sensory neurons, but in males PHC differentiates into a densely connected hub sensory neuron/interneuron, integrating a large number of male-specific synaptic inputs and conveying them to both male-specific and sex-shared circuitry. We show that the differentiation into such a hub neuron involves the sex-specific scaling of several components of the synaptic vesicle machinery, including the vesicular glutamate transporter eat-4/VGLUT, induction of neuropeptide expression, changes in axonal projection morphology, and a switch in neuronal function. We demonstrate that these molecular and anatomical remodeling events are controlled cell autonomously by the phylogenetically conserved Doublesex homolog dmd-3, which is both required and sufficient for sex-specific PHC differentiation. Cellular specificity of dmd-3 action is ensured by its collaboration with non-sex-specific terminal selector-type transcription factors, whereas the sex specificity of dmd-3 action is ensured by the hermaphrodite-specific transcriptional master regulator of hermaphroditic cell identity tra-1, which represses the transcription of dmd-3 in hermaphrodite PHC. Taken together, our studies provide mechanistic insights into how neurons are specified in a sexually dimorphic manner.

Indexed as

Cell DifferentiationAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsFemaleGene Expression Regulation, DevelopmentalMaleNeuronsSex CharacteristicsSex DifferentiationSynapsesTranscription FactorsCaenorhabditis elegans ProteinsTranscription Factors

Identifiers

PMID28065609
PMCPMC5805387
OpenAlexW2570405176

What OpenQuestion holds

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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.