Evidence map›Paper›PMID 42002805›Full record

ArticleBMC biology2026

Dynamic interplay of maternal and paternal contributions to offspring phenotype in Eurasian perch.

Rossella Debernardis, Abhipsa Panda, Sylwia Wałdowska, Katarzyna Palińska-Żarska, Christophe Klopp, Taina Rocha de Almeida, Sylwia Jarmołowicz, Piotr Hliwa, Daniel Żarski

Abstract read
In one paragraph

Article in BMC biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Rossella Debernardis *Team of Reproduction and Development in Fish, InLife Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, Poland.
Abhipsa Panda *Team of Reproduction and Development in Fish, InLife Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, Poland.
Sylwia WałdowskaTeam of Reproduction and Development in Fish, InLife Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, Poland.
Katarzyna Palińska-ŻarskaDepartment of Ichthyology, Hydrobiology and Aquatic Ecology, National Inland Fisheries Research Institute, Oczapowskiego 10, 10-719, Olsztyn, Poland.
Christophe KloppUniversité de Toulouse, GenoToul Bioinformatic Facility, Sigenae, BioinfOmics, UR875 MIAT, INRAE, Castanet-Tolosan, France.
Taina Rocha de AlmeidaTeam of Reproduction and Development in Fish, InLife Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, Poland.
Sylwia JarmołowiczDepartment of Ichthyology, Hydrobiology and Aquatic Ecology, National Inland Fisheries Research Institute, Oczapowskiego 10, 10-719, Olsztyn, Poland.
Piotr HliwaDepartment of Ichthyology and Aquaculture, University of Warmia and Mazury in Olsztyn, Oczapowskiego 5, 10-719, Olsztyn, Poland.
Daniel ŻarskiTeam of Reproduction and Development in Fish, InLife Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, Poland. d.zarski@pan.olsztyn.pl.

Funding

Narodowe Centrum Nauki UMO-2020/38/E/NZ9/00394
6 · The paper itself

Abstract

backgroundParental contributions to offspring phenotype extend beyond genetic inheritance, encompassing non-genetic factors that influence early development. However, the interplay between maternal and paternal effects remains poorly understood. This study investigates these contributions in Eurasian perch (Perca fluviatilis) - a valuable model to study parental effect in finfishes - by analyzing early life traits and transcriptomic profiles of larvae resulting from crosses between wild and domesticated parents.

resultsMaternal effects dominated key developmental traits, including hatching success, growth, and swim bladder inflation. Transcriptomic analysis revealed a complex regulatory interplay, with 573 genes under exclusive maternal control, while no genes were solely influenced by paternal input. Maternal-effect genes were primarily associated with metabolic, developmental, and stress-response pathways, shaping early larval physiology. Further analysis identified Eurasian-perch-specific candidate maternal-effect genes, such as crtac1, slc16a7, cox5b, kdr, cald1, and bin2, highlighting their potential role in early development. Although paternal contributions were limited, a subset of genes exhibited conditional paternal influence, suggesting a nuanced parental interplay in gene expression regulation.

conclusionsThese findings challenge the traditional perspective of strictly coordinated parental contributions, instead revealing a dynamic parental interplay over gene expression and offspring traits. The dominance of maternal effects suggests a primary role in shaping early development, while paternal factors may modulate expression patterns in a context-dependent manner. This study enhances our understanding of parental effects in fish, providing valuable insights for aquaculture breeding strategies and evolutionary biology research.

Indexed as

Maternal InheritancePaternal InheritancePerchesPhenotypeTranscriptomeAnimalsFemaleLarvaMaleDevelopmentFish larvaeMaternal-effect genesPaternal-effect genesTranscriptomics

Identifiers

PMID42002805
PMCPMC13224677

What Socratic holds

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LicenceCC BY
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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 Socratic graph.