Evidence map›Paper›PMID 26994290›Full record

ArticleG3 (Bethesda, Md.)2016

Genetic Background, Maternal Age, and Interaction Effects Mediate Rates of Crossing Over in Drosophila melanogaster Females.

Chad M Hunter, Matthew C Robinson, David L Aylor, Nadia D Singh

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Synaptonemal Complex-DeficientG3 (Bethesda, Md.) · 2020
    Article
  5. Article
  6. Article
  7. 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

4 authors.

Chad M HunterProgram in Genetics, Department of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27695 W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, North Carolina 27695 chadmhunter@ncsu.edu.ORCID 0000-0002-5249-4570
Matthew C RobinsonProgram in Genetics, Department of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27695 W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, North Carolina 27695.
David L AylorProgram in Genetics, Department of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27695 W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, North Carolina 27695 Bioinformatics Research Center, North Carolina State University, Raleigh, North Carolina 27695 Center for Human Health and the Environment, North Carolina State University, Raleigh, North Carolina 27695.
Nadia D SinghProgram in Genetics, Department of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27695 W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, North Carolina 27695 Bioinformatics Research Center, North Carolina State University, Raleigh, North Carolina 27695.

Funding

Epigenetics, environmental exposure, and reproduction in the Collaborative CrossR00ES021535 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI AYLOR, DAVID LAWRENCE · 2014 to 2016
$723k
NIEHS NIH HHS R00 ES021535
6 · The paper itself

Abstract

Meiotic recombination is a genetic process that is critical for proper chromosome segregation in many organisms. Despite being fundamental for organismal fitness, rates of crossing over vary greatly between taxa. Both genetic and environmental factors contribute to phenotypic variation in crossover frequency, as do genotype-environment interactions. Here, we test the hypothesis that maternal age influences rates of crossing over in a genotypic-specific manner. Using classical genetic techniques, we estimated rates of crossing over for individual Drosophila melanogaster females from five strains over their lifetime from a single mating event. We find that both age and genetic background significantly contribute to observed variation in recombination frequency, as do genotype-age interactions. We further find differences in the effect of age on recombination frequency in the two genomic regions surveyed. Our results highlight the complexity of recombination rate variation and reveal a new role of genotype by maternal age interactions in mediating recombination rate.

Indexed as

Crossing Over, GeneticGenetic BackgroundModels, GeneticAnimalsDrosophila melanogasterFemaleGenetic LociGenome, InsectGenomicsMaleMeiosisRecombination, Geneticagingmeiosisrecombination

Identifiers

PMID26994290
PMCPMC4856091

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.