Evidence map›Paper›PMID 26935419›Full record

ArticleG3 (Bethesda, Md.)2016

The Genetic Basis of Baculum Size and Shape Variation in Mice.

Nicholas G Schultz, Jesse Ingels, Andrew Hillhouse, Keegan Wardwell, Peter L Chang, James M Cheverud, Cathleen Lutz, Lu Lu, Robert W Williams, Matthew D Dean

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Dissection, MicroCT Scanning and Morphometric Analyses of the Baculum.Journal of visualized experiments : JoVE · 2017
    Article
  10. 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

10 authors.

Nicholas G SchultzMolecular and Computational Biology, Department of Biological Sciences, University of Southern California, Los Angeles, California 90089.
Jesse IngelsUniversity of Tennessee, Health Science Center, Memphis, Tennessee 38163.
Andrew HillhouseTexas A & M, Veterinary Medicine and Biomedical Sciences, College Station, Texas 77845.
Keegan WardwellThe Jackson Laboratory, Bar Harbor, Maine 04609.
Peter L ChangMolecular and Computational Biology, Department of Biological Sciences, University of Southern California, Los Angeles, California 90089.
James M CheverudLoyola University, Department of Biology, Chicago, Illinois 60626.
Cathleen LutzThe Jackson Laboratory, Bar Harbor, Maine 04609.
Lu LuUniversity of Tennessee, Health Science Center, Memphis, Tennessee 38163.
Robert W WilliamsUniversity of Tennessee, Health Science Center, Memphis, Tennessee 38163.
Matthew D DeanMolecular and Computational Biology, Department of Biological Sciences, University of Southern California, Los Angeles, California 90089 matthew.dean@usc.edu.

Funding

Use for ResourceP40OD011102 · OD · JACKSON LABORATORY · PI Steven Carmen Munger, Stephen A Murray · 2012 to 2026
$15.0M
Evolutionary and Functional Genetics of Male Reproduction using Wild Mice as a MoR01GM098536 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI DEAN, MATTHEW D · 2012 to 2016
$1.5M
NIGMS NIH HHS R01 GM098536
6 · The paper itself

Abstract

The rapid divergence of male genitalia is a preeminent evolutionary pattern. This rapid divergence is especially striking in the baculum, a bone that occurs in the penis of many mammalian species. Closely related species often display diverse baculum morphology where no other morphological differences can be discerned. While this fundamental pattern of evolution has been appreciated at the level of gross morphology, nearly nothing is known about the genetic basis of size and shape divergence. Quantifying the genetic basis of baculum size and shape variation has been difficult because these structures generally lack obvious landmarks, so comparing them in three dimensions is not straightforward. Here, we develop a novel morphometric approach to quantify size and shape variation from three-dimensional micro-CT scans taken from 369 bacula, representing 75 distinct strains of the BXD family of mice. We identify two quantitative trait loci (QTL) that explain ∼50% of the variance in baculum size, and a third QTL that explains more than 20% of the variance in shape. Together, our study demonstrates that baculum morphology may diverge relatively easily, with mutations at a few loci of large effect that independently modulate size and shape. Based on a combination of bioinformatic investigations and new data on RNA expression, we prioritized these QTL to 16 candidate genes, which have hypothesized roles in bone morphogenesis and may enable future genetic manipulation of baculum morphology.

Indexed as

Genetic Association StudiesGenetic VariationPhenotypeAnimalsBiological EvolutionBone and BonesComputational BiologyHigh-Throughput Nucleotide SequencingImaging, Three-DimensionalMating Preference, AnimalMiceQuantitative Trait LociSelection, GeneticX-Ray Microtomographybaculumsexual selectionshapesize

Identifiers

PMID26935419
PMCPMC4856068

What OpenQuestion holds

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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.