Evidence map›Paper›PMID 23106705›Full record

ArticleEvolution; international journal of organic evolution2012

Genomic basis of aging and life-history evolution in Drosophila melanogaster.

Silvia C Remolina, Peter L Chang, Jeff Leips, Sergey V Nuzhdin, Kimberly A Hughes

Open access · greenAbstract read
In one paragraph

Article in Evolution; international journal of organic evolution, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed, 1 pooled it
8.5field-weighted citation impact, top 2% 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

79 citing papers in PubMed, 1 synthesis or guideline pooled it, 152 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Beyond Fixation: Persistent Genetic Variation Under Intense Selection.bioRxiv : the preprint server for biology · 2026
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  14. Natural alleles at theProceedings. Biological sciences · 2022
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  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

19 more citing papers are in PubMed but not listed here.

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

5 authors at 4 institutions in 1 country.

Silvia C RemolinaDepartment of Animal Biology, University of Illinois, Urbana-Champaign, 505 S. Goodwin Ave, Urbana, Illinois 61801, USA.
Peter L Chang
Jeff Leips
Sergey V Nuzhdin
Kimberly A Hughes
University of Southern California · USFlorida State University · USUniversity of Illinois Urbana-Champaign · USUniversity of Maryland, Baltimore County · US

Funding

Implications of haplotype structure in the human genomeP50HG002790 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TAVARE, SIMON · 2003 to 2013
$29.9M
Research DevelopmentP30AG013283 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MILLER, RICHARD A · 1995 to 2014
$12.3M
Molecular mechanisms of queen bee longevityR01AG022824 · NIA · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI ROBINSON, GENE E · 2003 to 2006
$1.2M
BIOLOGICAL CAUSES OF MORTALITY PLATEAUS IN DROSOPHILAR03AG018122 · NIA · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI HUGHES, KIMBERLY A. · 2000 to 2000
$77k
NHGRI NIH HHS HG002790NHGRI NIH HHS P50 HG002790NIA NIH HHS AG022824NIA NIH HHS P30 AG013283NIA NIH HHS R01 AG022824NIA NIH HHS R03 AG018122
6 · The paper itself

Abstract

Natural diversity in aging and other life-history patterns is a hallmark of organismal variation. Related species, populations, and individuals within populations show genetically based variation in life span and other aspects of age-related performance. Population differences are especially informative because these differences can be large relative to within-population variation and because they occur in organisms with otherwise similar genomes. We used experimental evolution to produce populations divergent for life span and late-age fertility and then used deep genome sequencing to detect sequence variants with nucleotide-level resolution. Several genes and genome regions showed strong signatures of selection, and the same regions were implicated in independent comparisons, suggesting that the same alleles were selected in replicate lines. Genes related to oogenesis, immunity, and protein degradation were implicated as important modifiers of late-life performance. Expression profiling and functional annotation narrowed the list of strong candidate genes to 38, most of which are novel candidates for regulating aging. Life span and early age fecundity were negatively correlated among populations; therefore, the alleles we identified also are candidate regulators of a major life-history trade-off. More generally, we argue that hitchhiking mapping can be a powerful tool for uncovering the molecular bases of quantitative genetic variation.

Indexed as

Biological EvolutionSelection, GeneticAgingAnimalsBase SequenceChromosome MappingDrosophila melanogasterFemaleFertilityGene Expression ProfilingGene FrequencyGenes, InsectGenomeMalePolymorphism, GeneticRNA, MessengerRNA, Messenger

Identifiers

PMID23106705
PMCPMC4539122
OpenAlexW1598363823

What OpenQuestion holds

Textmetadata
LicenceTDM
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.