Evidence map›Paper›PMID 32707065›Full record

ArticleCurrent biology : CB2020

Dynamic, Non-binary Specification of Sexual State in the C. elegans Nervous System.

Hannah N Lawson, Leigh R Wexler, Hayley K Wnuk, Douglas S Portman

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Sex Alters Hypoxic Responses inmicroPublication biology · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Designing and Teaching Courses on Sex, Gender, and the Brain: Two Implementations in the Undergraduate Classroom.Journal of undergraduate neuroscience education : JUNE : a publication of FUN, Faculty for Undergraduate Neuroscience · 2024
    Article
  7. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Hannah N LawsonDepartment of Biology, University of Rochester, Rochester, NY, USA.
Leigh R WexlerDepartment of Biomedical Genetics, University of Rochester, Rochester, NY, USA.
Hayley K WnukDepartment of Biology, University of Rochester, Rochester, NY, USA.
Douglas S PortmanDepartment of Biology, University of Rochester, Rochester, NY, USA; Department of Biomedical Genetics, University of Rochester, Rochester, NY, USA; Ernest J. Del Monte Institute for Neuroscience, University of Rochester, Rochester, NY, USA. Electronic address: douglas.portman@rochester.edu.
University of Rochester · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Neurogenetic mechanisms of sensory circuit plasticityR01GM130136 · NIGMS · UNIVERSITY OF ROCHESTER · PI PORTMAN, DOUGLAS S · 2018 to 2021
$1.2M
Genetic and Hormonal Mechanisms of Sex Differences in the Nervous SystemR01GM108885 · NIGMS · UNIVERSITY OF ROCHESTER · PI PORTMAN, DOUGLAS S · 2014 to 2017
$1.1M
NIGMS NIH HHS R01 GM108885NIGMS NIH HHS R01 GM130136NIH HHS P40 OD010440
6 · The paper itself

Abstract

Biological sex in animals is often considered a fixed, individual-level characteristic. However, not all sex-specific features are static: for example, C. elegans males (XO) can sometimes exhibit hermaphrodite (XX)-like feeding behavior [1, 2]. (C. elegans hermaphrodites are somatic females that transiently produce self-sperm.) Essentially all somatic sex differences in C. elegans are governed by the master regulator tra-1, whose activity is controlled by chromosomal sex and is necessary and sufficient to specify the hermaphrodite state [3]. One aspect of this state is high expression of the chemoreceptor odr-10. In hermaphrodites, high odr-10 expression promotes feeding, but in males, low odr-10 expression facilitates exploration [4]. However, males suppress this sex difference in two contexts: juvenile males exhibit high odr-10 expression and food deprivation activates odr-10 in adult males [4-6]. Remarkably, we find that both of these phenomena require tra-1. In juvenile (L3) males, tra-1 is expressed in numerous neurons; this expression diminishes as individuals mature into adulthood, a process that requires conserved regulators of sexual maturation. tra-1 remains expressed in a small number of neurons in adult males, where it likely has a permissive role in odr-10 activation. Thus, the neuronal functions of tra-1 are not limited to hermaphrodites; rather, tra-1 also acts in the male nervous system to transiently suppress a sexual dimorphism, developmentally and in response to nutritional stress. Our results show that the molecular and functional representation of sexual state in C. elegans is neither static nor homogeneous, challenging traditional notions about the nature of biological sex.

Indexed as

Gene Expression RegulationSex CharacteristicsAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsDNA-Binding ProteinsFemaleMaleNervous SystemReceptors, Cytoplasmic and NuclearSex FactorsTranscription FactorsCaenorhabditis elegans ProteinsDAF-12 protein, C elegansDNA-Binding ProteinsReceptors, Cytoplasmic and Nucleartra-1 protein, C elegansTranscription Factorsbiological sexchemosensationdevelopmental timingsex determinationsex differencesexual differentiationsexual dimorphismsexual maturation

Identifiers

PMID32707065
PMCPMC7511423
OpenAlexW3045379396

What OpenQuestion holds

Textmetadata
LicenceTDM
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.