Evidence map›Paper›PMID 32203250›Full record

ArticleHeredity2020

The complex genetic architecture of male mate choice evolution between Drosophila species.

Michael P Shahandeh, Thomas L Turner

Open access · bronzeAbstract read
In one paragraph

Article in Heredity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Genetics and the Evolution of Prezygotic Isolation.Cold Spring Harbor perspectives in biology · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. 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

2 authors at 1 institution in 1 country.

Michael P ShahandehDepartment of Ecology, Evolution, and Marine Biology, University of California, Santa Barbara, USA. mshahandeh@ucsb.edu.ORCID 0000-0002-0729-6989
Thomas L TurnerDepartment of Ecology, Evolution, and Marine Biology, University of California, Santa Barbara, USA.
University of California, Santa Barbara · US

Funding

Evolutionary Behavioral Genomics of Drosophila CourtshipR01GM098614 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI TURNER, THOMAS LEE · 2011 to 2015
$1.4M
NIGMS NIH HHS R01 GM098614
6 · The paper itself

Abstract

Mate choice behaviors are among the most important reproductive isolating barriers in many animals. Little is known about the genetic basis of reproductively isolating behaviors, but examples to date provide evidence that they can have a simple genetic basis. However, it is unclear if these results indicate that individual genes with large effects are common, or are instead due to ascertainment biases. Here, we present the results of a QTL mapping study for the most important behavioral isolating barrier between Drosophila simulans and D. sechellia: male mate choice. Our QTL results initially suggested that differences in male mate choice may be due to a couple loci with large effects. However, as we divided the largest-effect QTL using stable introgression strains, we found evidence of multiple interacting loci. We further find that separate regions of the genome control different aspects of male choice. Taken together, our results suggest that the genetic architecture of mate choice behavior, in this case, is more complex than QTL mapping suggested, highlighting potential challenges to future mapping studies. We discuss the implications of these results as they relate to signal-receiver coevolution, mate choice, and reproductive isolation.

Indexed as

DrosophilaMating Preference, AnimalQuantitative Trait LociAnimalsChromosome MappingDrosophila simulansMaleReproductive Isolation

Identifiers

PMID32203250
PMCPMC7239879
OpenAlexW3011128227

What OpenQuestion holds

Textmetadata
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.