Evidence map›Paper›PMID 20488933›Full record

ArticleGenome research2010

Genome-wide gene expression regulation as a function of genotype and age in C. elegans.

Ana Viñuela, L Basten Snoek, Joost A G Riksen, Jan E Kammenga

Abstract read
In one paragraph

Article in Genome research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing 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

86 citing papers in PubMed.

  1. Article
  2. Article
  3. Genetic mapping of lifespan and mitochondrial stress response inbioRxiv : the preprint server for biology · 2025
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  4. The regulatory architecture of gene expression variation inbioRxiv : the preprint server for biology · 2025
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  7. Article
  8. Article
  9. Quantifying transcriptome diversity: a review.Briefings in functional genomics · 2024
    Review
  10. Article
  11. High-content phenotypic analysis ofbioRxiv : the preprint server for biology · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Plasticity of maternal environment-dependent expression-QTLs of tomato seeds.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2023
    Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article

26 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

4 authors.

Ana ViñuelaLaboratory of Nematology, Wageningen University, 6708 PB Wageningen, The Netherlands.
L Basten Snoek
Joost A G Riksen
Jan E Kammenga

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene expression becomes more variable with age, and it is widely assumed that this is due to a decrease in expression regulation. But currently there is no understanding how gene expression regulatory patterns progress with age. Here we explored genome-wide gene expression variation and regulatory loci (eQTL) in a population of developing and aging C. elegans recombinant inbred worms. We found almost 900 genes with an eQTL, of which almost half were found to have a genotype-by-age effect ((gxa)eQTL). The total number of eQTL decreased with age, whereas the variation in expression increased. In developing worms, the number of genes with increased expression variation (1282) was similar to the ones with decreased expression variation (1328). In aging worms, the number of genes with increased variation (1772) was nearly five times higher than the number of genes with a decreased expression variation (373). The number of cis-acting eQTL in juveniles decreased by almost 50% in old worms, whereas the number of trans-acting loci decreased by approximately 27%, indicating that cis-regulation becomes relatively less frequent than trans-regulation in aging worms. Of the 373 genes with decreased expression level variation in aging worms, approximately 39% had an eQTL compared with approximately 14% in developing worms. (gxa)eQTL were found for approximately 21% of these genes in aging worms compared with only approximately 6% in developing worms. We highlight three examples of linkages: in young worms (pgp-6), in old worms (daf-16), and throughout life (lips-16). Our findings demonstrate that eQTL patterns are strongly affected by age, and suggest that gene network integrity declines with age.

Indexed as

Gene Expression RegulationGenomeAgingAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsChromosome MappingForkhead Transcription FactorsGene Expression ProfilingGene Expression Regulation, DevelopmentalGenetic LociGenetic MarkersGenetic VariationGenotypeQuantitative Trait LociTranscription FactorsCaenorhabditis elegans Proteinsdaf-16 protein, C elegansForkhead Transcription FactorsGenetic MarkersTranscription Factors

Identifiers

PMID20488933
PMCPMC2892094

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Registered trials

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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.