Evidence map›Paper›PMID 24440396›Full record

ArticleCurrent biology : CB2014

Male-specific fruitless isoforms target neurodevelopmental genes to specify a sexually dimorphic nervous system.

Megan C Neville, Tetsuya Nojima, Elizabeth Ashley, Darren J Parker, John Walker, Tony Southall, Bram Van de Sande, Ana C Marques, Bettina Fischer, Andrea H Brand and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

68 citing papers in PubMed, 114 citations in OpenAlex.

  1. Article
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  7. Sexual dimorphism in the complete connectome of thebioRxiv : the preprint server for biology · 2025
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  8. A single-nucleus transcriptomic atlas of the adultbioRxiv : the preprint server for biology · 2025
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  13. Genetic Coupling of Mate Recognition Systems in the Genomic Era.Cold Spring Harbor perspectives in biology · 2024
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. TheProceedings. Biological sciences · 2022
    Article

8 more citing papers are in PubMed but not listed here.

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

14 authors at 5 institutions in 2 countries.

Megan C NevilleDepartment of Physiology, Anatomy and Genetics, University of Oxford, Sherrington Building, Parks Road, Oxford OX1 3PT, UK. Electronic address: megan.goodwin@dpag.ox.ac.uk.
Tetsuya NojimaDepartment of Physiology, Anatomy and Genetics, University of Oxford, Sherrington Building, Parks Road, Oxford OX1 3PT, UK.
Elizabeth AshleyDepartment of Physiology, Anatomy and Genetics, University of Oxford, Sherrington Building, Parks Road, Oxford OX1 3PT, UK.
Darren J ParkerCentre for Biological Diversity, University of St Andrews, St Andrews, KY16 9TH, UK.
John WalkerDepartment of Physiology, Anatomy and Genetics, University of Oxford, Sherrington Building, Parks Road, Oxford OX1 3PT, UK.
Tony SouthallThe Gurdon Institute and Department of Physiology, Development and Neuroscience, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK.
Bram Van de SandeLaboratory of Computational Biology, Department of Human Genetics, University of Leuven, 3000 Leuven, Belgium.
Ana C MarquesDepartment of Physiology, Anatomy and Genetics, University of Oxford, Sherrington Building, Parks Road, Oxford OX1 3PT, UK.
Bettina FischerCambridge Systems Biology Centre, University of Cambridge, Tennis Court Road, Cambridge CB2 1QR, UK; Department of Genetics, University of Cambridge, Downing Street, Cambridge CB2 3EH, UK.
Andrea H BrandThe Gurdon Institute and Department of Physiology, Development and Neuroscience, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK.
Steven RussellCambridge Systems Biology Centre, University of Cambridge, Tennis Court Road, Cambridge CB2 1QR, UK; Department of Genetics, University of Cambridge, Downing Street, Cambridge CB2 3EH, UK.
Michael G RitchieCentre for Biological Diversity, University of St Andrews, St Andrews, KY16 9TH, UK.
Stein AertsLaboratory of Computational Biology, Department of Human Genetics, University of Leuven, 3000 Leuven, Belgium.
Stephen F GoodwinDepartment of Physiology, Anatomy and Genetics, University of Oxford, Sherrington Building, Parks Road, Oxford OX1 3PT, UK. Electronic address: stephen.goodwin@dpag.ox.ac.uk.
University of Oxford · GBUniversity of Cambridge · GBKU Leuven · BEUniversity of St Andrews · GBWellcome/Cancer Research UK Gurdon Institute · GB

Funding

Drosophila Transgenic RNAi Resource ProjectR01GM084947 · NIGMS · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2008 to 2019
$9.8M
Biotechnology and Biological Sciences Research Council BBS/B/0837XNIGMS NIH HHS R01 GM084947NIGMS NIH HHS R01-GM084947Wellcome Trust 092096Wellcome Trust WT082987MFWellcome Trust WT085521MA
6 · The paper itself

Abstract

backgroundIn Drosophila, male courtship behavior is regulated in large part by the gene fruitless (fru). fru encodes a set of putative transcription factors that promote male sexual behavior by controlling the development of sexually dimorphic neuronal circuitry. Little is known about how Fru proteins function at the level of transcriptional regulation or the role that isoform diversity plays in the formation of a male-specific nervous system.

resultsTo characterize the roles of sex-specific Fru isoforms in specifying male behavior, we generated novel isoform-specific mutants and used a genomic approach to identify direct Fru isoform targets during development. We demonstrate that all Fru isoforms directly target genes involved in the development of the nervous system, with individual isoforms exhibiting unique binding specificities. We observe that fru behavioral phenotypes are specified by either a single isoform or a combination of isoforms. Finally, we illustrate the utility of these data for the identification of novel sexually dimorphic genomic enhancers and novel downstream regulators of male sexual behavior.

conclusionsThese findings suggest that Fru isoform diversity facilitates both redundancy and specificity in gene expression, and that the regulation of neuronal developmental genes may be the most ancient and conserved role of fru in the specification of a male-specific nervous system.

Indexed as

Sex CharacteristicsAnimalsBase SequenceCentral Nervous SystemDrosophila melanogasterDrosophila ProteinsGene Expression Regulation, DevelopmentalGene Knockout TechniquesMaleMolecular Sequence DataNerve Tissue ProteinsNeurogenesisProtein IsoformsSexual Behavior, AnimalTranscription FactorsDrosophila Proteinsfru protein, DrosophilaNerve Tissue ProteinsProtein IsoformsTranscription Factors

Identifiers

PMID24440396
PMCPMC3969260
OpenAlexW2152660732

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.