Evidence map›Paper›PMID 38557670›Full record

ArticlePloS one2024

Reproductive system, temperature, and genetic background effects in experimentally evolving populations of Caenorhabditis elegans.

Joanna K Baran, Paulina Kosztyła, Weronika Antoł, Marta K Labocha, Karolina Sychta, Szymon M Drobniak, Zofia M Prokop

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. P-glycoproteins and amphids: a two-stage trajectory of ivermectin resistance in Caenorhabditis elegans.International journal for parasitology. Drugs and drug resistance · 2026
    Article
  2. 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

7 authors at 2 institutions in 2 countries.

Joanna K BaranFaculty of Biology, Institute of Environmental Sciences, Jagiellonian University in Krakow, Krakow, Poland.
Paulina KosztyłaFaculty of Biology, Institute of Environmental Sciences, Jagiellonian University in Krakow, Krakow, Poland.
Weronika AntołFaculty of Biology, Institute of Environmental Sciences, Jagiellonian University in Krakow, Krakow, Poland.ORCID 0000-0003-2047-330X
Marta K LabochaFaculty of Biology, Institute of Environmental Sciences, Jagiellonian University in Krakow, Krakow, Poland.
Karolina SychtaInstitute of Systematics and Evolution of Animals, Polish Academy of Sciences, Krakow, Poland.
Szymon M DrobniakFaculty of Biology, Institute of Environmental Sciences, Jagiellonian University in Krakow, Krakow, Poland.
Zofia M ProkopFaculty of Biology, Institute of Environmental Sciences, Jagiellonian University in Krakow, Krakow, Poland.ORCID 0000-0001-8790-6654
Jagiellonian University · PLInstitute of Systematics and Evolution of Animals · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Experimental evolution (EE) is a powerful research framework for gaining insights into many biological questions, including the evolution of reproductive systems. We designed a long-term and highly replicated EE project using the nematode C. elegans, with the main aim of investigating the impact of reproductive system on adaptation and diversification under environmental challenge. From the laboratory-adapted strain N2, we derived isogenic lines and introgressed the fog-2(q71) mutation, which changes the reproductive system from nearly exclusive selfing to obligatory outcrossing, independently into 3 of them. This way, we obtained 3 pairs of isogenic ancestral populations differing in reproductive system; from these, we derived replicate EE populations and let them evolve in either novel (increased temperature) or control conditions for over 100 generations. Subsequently, fitness of both EE and ancestral populations was assayed under the increased temperature conditions. Importantly, each population was assayed in 2-4 independent blocks, allowing us to gain insight into the reproducibility of fitness scores. We expected to find upward fitness divergence, compared to ancestors, in populations which had evolved in this treatment, particularly in the outcrossing ones due to the benefits of genetic shuffling. However, our data did not support these predictions. The first major finding was very strong effect of replicate block on populations' fitness scores. This indicates that despite standardization procedures, some important environmental effects were varying among blocks, and possibly compounded by epigenetic inheritance. Our second key finding was that patterns of EE populations' divergence from ancestors differed among the ancestral isolines, suggesting that research conclusions derived for any particular genetic background should never be generalized without sampling a wider set of backgrounds. Overall, our results support the calls to pay more attention to biological variability when designing studies and interpreting their results, and to avoid over-generalizations of outcomes obtained for specific genetic and/or environmental conditions.

Indexed as

Caenorhabditis elegansGenitaliaAnimalsBiological EvolutionGenetic BackgroundReproducibility of ResultsTemperature

Identifiers

PMID38557670
PMCPMC10984399
OpenAlexW4393393436

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.