Evidence map›Paper›PMID 38520538›Full record

ArticleJournal of comparative physiology. B, Biochemical, systemic, and environmental physiology2024

Embryonic methionine triggers post-natal developmental programming in Japanese quail.

Sawadi F Ndunguru, Gebrehaweria K Reda, Brigitta Csernus, Renáta Knop, Gabriella Gulyás, Csaba Szabó, Levente Czeglédi, Ádám Z Lendvai

Open access · hybridAbstract read
In one paragraph

Article in Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
14.4field-weighted citation impact, top 1% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Sawadi F NdunguruDepartment of Animal Science, Faculty of Agricultural and Food Sciences and Environmental Management, Institute of Animal Science, Biotechnology and Nature Conservation, University of Debrecen, Debrecen, 4032, Hungary. ndunguru@agr.unideb.hu.ORCID 0000-0001-5945-5614
Gebrehaweria K RedaDepartment of Animal Science, Faculty of Agricultural and Food Sciences and Environmental Management, Institute of Animal Science, Biotechnology and Nature Conservation, University of Debrecen, Debrecen, 4032, Hungary.ORCID 0000-0002-2193-3390
Brigitta CsernusDepartment of Evolutionary Zoology and Human Biology, University of Debrecen, Debrecen, 4032, Hungary.
Renáta KnopDepartment of Animal Science, Faculty of Agricultural and Food Sciences and Environmental Management, Institute of Animal Science, Biotechnology and Nature Conservation, University of Debrecen, Debrecen, 4032, Hungary.
Gabriella GulyásDepartment of Animal Science, Faculty of Agricultural and Food Sciences and Environmental Management, Institute of Animal Science, Biotechnology and Nature Conservation, University of Debrecen, Debrecen, 4032, Hungary.
Csaba SzabóDepartment of Animal Nutrition and Physiology, Faculty of Agriculture and Food Sciences and Environmental Management, University of Debrecen, Debrecen, 4032, Hungary.
Levente CzeglédiDepartment of Animal Science, Faculty of Agricultural and Food Sciences and Environmental Management, Institute of Animal Science, Biotechnology and Nature Conservation, University of Debrecen, Debrecen, 4032, Hungary.
Ádám Z LendvaiDepartment of Evolutionary Zoology and Human Biology, University of Debrecen, Debrecen, 4032, Hungary. az.lendvai@gmail.com.ORCID 0000-0002-8953-920X
University of Debrecen · HU

Funding

Hungarian Scientific Research Fund grant N. K139021Tempus Közalapítvány SHE-34302-004/2020
6 · The paper itself

Abstract

Embryonic development is one of the most sensitive and critical stages when maternal effects may influence the offspring's phenotype. In birds and other oviparous species, embryonic development is confined to the eggs, therefore females must deposit resources into the eggs to prepare the offspring for the prevailing post-natal conditions. However, the mechanisms of such phenotypic adjustments remain poorly understood. We simulated a maternal nutritional transfer by injecting 1 mg of L-methionine solution into Japanese quail eggs before the onset of incubation. The increase in early methionine concentration in eggs activated the insulin/insulin-like signalling and mechanistic target of rapamycin (IIS/mTOR) signalling pathways and affected post-natal developmental trajectories. Chicks from methionine-supplemented eggs had higher expression of liver IGF1 and mTOR genes at hatching but were similar in size, and the phenotypic effects of increased growth became apparent only a week later and remained up to three weeks. Circulating levels of insulin-like growth factor-1 (IGF-1) and expression of ribosomal protein serine 6 kinase 1 (RPS6K1), the mTOR downstream effector, were elevated only three weeks after hatching. These results show that specific nutritional cues may have phenotypic programming effects by sequentially activating specific nutrient-sensing pathways and achieving transgenerational phenotypic plasticity.

Indexed as

CoturnixInsulin-Like Growth Factor IMethionineTOR Serine-Threonine KinasesAnimalsEmbryonic DevelopmentEmbryo, NonmammalianFemaleInsulinLiverSignal TransductionInsulinInsulin-Like Growth Factor IMethionineTOR Serine-Threonine KinasesAmino acidGrowthIGF1l-methioninemTOR

Identifiers

PMID38520538
PMCPMC11070397
OpenAlexW4393115820

What Socratic 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 Socratic graph.