Evidence map›Paper›PMID 25729562›Full record

ArticleBiology of sex differences2014

Examination of the genetic basis for sexual dimorphism in the Aedes aegypti (dengue vector mosquito) pupal brain.

Michael Tomchaney, Keshava Mysore, Longhua Sun, Ping Li, Scott J Emrich, David W Severson, Molly Duman-Scheel

Open access · goldAbstract read
In one paragraph

Article in Biology of sex differences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  3. A Conserved Female-Specific Requirement for thePathogens (Basel, Switzerland) · 2022
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  20. Developmental neurogenetics of sexual dimorphism inFrontiers in ecology and evolution
    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

7 authors at 1 institution in 1 country.

Michael TomchaneyEck Institute for Global Health, Galvin Life Sciences, University of Notre Dame, Notre Dame 46556, IN, USA ; Department of Biological Sciences, Galvin Life Sciences, University of Notre Dame, Notre Dame 46556, IN, USA.
Keshava MysoreEck Institute for Global Health, Galvin Life Sciences, University of Notre Dame, Notre Dame 46556, IN, USA ; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Raclin-Carmichael Hall, South Bend 46617, IN, USA.
Longhua SunEck Institute for Global Health, Galvin Life Sciences, University of Notre Dame, Notre Dame 46556, IN, USA ; Department of Biological Sciences, Galvin Life Sciences, University of Notre Dame, Notre Dame 46556, IN, USA.
Ping LiEck Institute for Global Health, Galvin Life Sciences, University of Notre Dame, Notre Dame 46556, IN, USA ; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Raclin-Carmichael Hall, South Bend 46617, IN, USA.
Scott J EmrichEck Institute for Global Health, Galvin Life Sciences, University of Notre Dame, Notre Dame 46556, IN, USA ; Department of Computer Science and Engineering, University of Notre Dame, Notre Dame 46556, IN, USA.
David W SeversonEck Institute for Global Health, Galvin Life Sciences, University of Notre Dame, Notre Dame 46556, IN, USA ; Department of Biological Sciences, Galvin Life Sciences, University of Notre Dame, Notre Dame 46556, IN, USA ; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Raclin-Carmichael Hall, South Bend 46617, IN, USA.
Molly Duman-ScheelEck Institute for Global Health, Galvin Life Sciences, University of Notre Dame, Notre Dame 46556, IN, USA ; Department of Biological Sciences, Galvin Life Sciences, University of Notre Dame, Notre Dame 46556, IN, USA ; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Raclin-Carmichael Hall, South Bend 46617, IN, USA.
University of Notre Dame · US

Funding

Analysis of the functions of axon guidance genes during vector mosquito developmeR01AI081795 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI SCHEEL, MOLLY DUMAN · 2009 to 2012
$1.5M
NIAID NIH HHS R01 AI081795
6 · The paper itself

Abstract

backgroundMost animal species exhibit sexually dimorphic behaviors, many of which are linked to reproduction. A number of these behaviors, including blood feeding in female mosquitoes, contribute to the global spread of vector-borne illnesses. However, knowledge concerning the genetic basis of sexually dimorphic traits is limited in any organism, including mosquitoes, especially with respect to differences in the developing nervous system.

methodsCustom microarrays were used to examine global differences in female vs. male gene expression in the developing pupal head of the dengue vector mosquito, Aedes aegypti. The spatial expression patterns of a subset of differentially expressed transcripts were examined in the developing female vs. male pupal brain through in situ hybridization experiments. Small interfering RNA (siRNA)-mediated knockdown studies were used to assess the putative role of Doublesex, a terminal component of the sex determination pathway, in the regulation of sex-specific gene expression observed in the developing pupal brain.

resultsTranscripts (2,527), many of which were linked to proteolysis, the proteasome, metabolism, catabolic, and biosynthetic processes, ion transport, cell growth, and proliferation, were found to be differentially expressed in A. aegypti female vs. male pupal heads. Analysis of the spatial expression patterns for a subset of dimorphically expressed genes in the pupal brain validated the data set and also facilitated the identification of brain regions with dimorphic gene expression. In many cases, dimorphic gene expression localized to the optic lobe. Sex-specific differences in gene expression were also detected in the antennal lobe and mushroom body. siRNA-mediated gene targeting experiments demonstrated that Doublesex, a transcription factor with consensus binding sites located adjacent to many dimorphically expressed transcripts that function in neural development, is required for regulation of sex-specific gene expression in the developing A. aegypti brain.

conclusionsThese studies revealed sex-specific gene expression profiles in the developing A. aegypti pupal head and identified Doublesex as a key regulator of sexually dimorphic gene expression during mosquito neural development.

Indexed as

Aedes aegyptiBrainDevelopmentDimorphismDoublesexMosquitoNervous systemOptic lobePupaeVector

Identifiers

PMID25729562
PMCPMC4342991
OpenAlexW2149385868

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.