Evidence map›Paper›PMID 25783699›Full record

ArticleGenetics2015

Genetic architecture and functional characterization of genes underlying the rapid diversification of male external genitalia between Drosophila simulans and Drosophila mauritiana.

Kentaro M Tanaka, Corinna Hopfen, Matthew R Herbert, Christian Schlötterer, David L Stern, John P Masly, Alistair P McGregor, Maria D S Nunes

Abstract read
In one paragraph

Article in Genetics, 2015. 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

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3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. Article
  2. A developmental atlas of male terminalia across twelve species ofFrontiers in cell and developmental biology · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  9. Article
  10. Article
  11. Genetic and Transgenic Reagents forG3 (Bethesda, Md.) · 2017
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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

8 authors.

Kentaro M TanakaDepartment of Biological and Medical Sciences, Oxford Brookes University, Oxford, OX3 0BP, United Kingdom.
Corinna HopfenInstitut für Populationsgenetik, Veterinärmedizinische Universität Wien, A-1210, Vienna, Austria.
Matthew R HerbertDepartment of Biological and Medical Sciences, Oxford Brookes University, Oxford, OX3 0BP, United Kingdom.
Christian SchlöttererInstitut für Populationsgenetik, Veterinärmedizinische Universität Wien, A-1210, Vienna, Austria.
David L SternJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, Virginia 20147.
John P MaslyDepartment of Biology, University of Oklahoma, Norman, Oklahoma 73019.
Alistair P McGregorDepartment of Biological and Medical Sciences, Oxford Brookes University, Oxford, OX3 0BP, United Kingdom msantos-nunes@brookes.ac.uk amcgregor@brookes.ac.uk.
Maria D S NunesDepartment of Biological and Medical Sciences, Oxford Brookes University, Oxford, OX3 0BP, United Kingdom msantos-nunes@brookes.ac.uk amcgregor@brookes.ac.uk.

Funding

European Research Council 242553
6 · The paper itself

Abstract

Male sexual characters are often among the first traits to diverge between closely related species and identifying the genetic basis of such changes can contribute to our understanding of their evolutionary history. However, little is known about the genetic architecture or the specific genes underlying the evolution of male genitalia. The morphology of the claspers, posterior lobes, and anal plates exhibit striking differences between Drosophila mauritiana and D. simulans. Using QTL and introgression-based high-resolution mapping, we identified several small regions on chromosome arms 3L and 3R that contribute to differences in these traits. However, we found that the loci underlying the evolution of clasper differences between these two species are independent from those that contribute to posterior lobe and anal plate divergence. Furthermore, while most of the loci affect each trait in the same direction and act additively, we also found evidence for epistasis between loci for clasper bristle number. In addition, we conducted an RNAi screen in D. melanogaster to investigate if positional and expression candidate genes located on chromosome 3L, are also involved in genital development. We found that six of these genes, including components of Wnt signaling and male-specific lethal 3 (msl3), regulate the development of genital traits consistent with the effects of the introgressed regions where they are located and that thus represent promising candidate genes for the evolution these traits.

Indexed as

Drosophila ProteinsGenetic SpeciationGenetic VariationNuclear ProteinsTranscription FactorsAnimalsDrosophilaEpistasis, GeneticGenetic PleiotropyGenitalia, MaleMaleQuantitative Trait LociDrosophila Proteinsmsl-3 protein, DrosophilaNuclear ProteinsTranscription FactorsdominanceDrosophilaepistasisgenital archpleiotropyquantitative trait

Identifiers

PMID25783699
PMCPMC4423377

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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.