Evidence map›Paper›PMID 16272414›Full record

ArticleGenetics2006

Quantitative trait loci with age-specific effects on fecundity in Drosophila melanogaster.

Jeff Leips, Paul Gilligan, Trudy F C Mackay

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

25 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Age influences the thermal suitability ofProceedings. Biological sciences · 2020
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  6. Review
  7. Article
  8. Review
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  10. Review
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  13. Detecting genetic variants for extreme aging using multiple data sources.European journal of human genetics : EJHG · 2013
    Article
  14. Article
  15. Article
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  19. Article
  20. Mutation and the evolution of ageing: from biometrics to system genetics.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2010
    Review
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

3 authors at 1 institution in 1 country.

Jeff LeipsDepartment of Biological Sciences, University of Maryland Baltimore County, Baltimore 21250, USA. leips@umbc.edu
Paul Gilligan
Trudy F C Mackay
North Carolina State University · US

Funding

THEORETICAL QUANTITATIVE GENETICSP01GM045344 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI GIBSON, GREGORY C. · 1991 to 2005
$7.2M
QUANTITATIVE GENETICS OF DROSOPHILA LIFE HISTORY TRAITSF32GM018818 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI LEIPS, JEFFERY · 1997 to 1999
–
NIGMS NIH HHS F32 GM018818NIGMS NIH HHS GM18818-03NIGMS NIH HHS GM45344NIGMS NIH HHS P01 GM045344
6 · The paper itself

Abstract

Life-history theory and evolutionary theories of aging assume the existence of alleles with age-specific effects on fitness. While various studies have documented age-related changes in the genetic contribution to variation in fitness components, we know very little about the underlying genetic architecture of such changes. We used a set of recombinant inbred lines to map and characterize the effects of quantitative trait loci (QTL) affecting fecundity of Drosophila melanogaster females at 1 and 4 weeks of age. We identified one QTL on the second chromosome and one or two QTL affecting fecundity on the third chromosome, but these QTL affected fecundity only at 1 week of age. There was more genetic variation for fecundity at 4 weeks of age than at 1 week of age and there was no genetic correlation between early and late-age fecundity. These results suggest that different loci contribute to the variation in fecundity as the organism ages. Our data provide support for the mutation accumulation theory of aging as applied to reproductive senescence. Comparing the results from this study with our previous work on life-span QTL, we also find evidence that antagonistic pleiotropy may contribute to the genetic basis of senescence in these lines as well.

Indexed as

Quantitative Trait LociAgingAnimalsAnimals, Inbred StrainsDrosophila melanogasterEpistasis, GeneticFemaleFertilityGenetic MarkersGenetic VariationMaleGenetic Markers

Identifiers

PMID16272414
PMCPMC1456283
OpenAlexW2137096448

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.