Level D· Scientific groundwork from lab and animal studiesLaboratory StudyEurope PMCOpen access

Comparative Transcriptome Analysis of Orbital Fat Reveals Stage-Specific Gene Expression Associated with Growth Variation in Bighead Carp (<i>Hypophthalmichthys nobilis</i>)

Wang J., Lei Q., Liu J., Tian H., Yao G., Sun Z.

Laboratory Study, published in Animals (Basel) (2026) — summary generated from the PubMed abstract.

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Level D· Scientific groundwork from lab and animal studiesEvidence level of this study

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
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This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Laboratory Study
Journal
Animals (Basel) (2026)
Reported sample size
—
Source database
Europe PMC
PMID
41829011
PMCID
PMC12984460
DOI
10.3390/ani16050803

Abstract (original English)

Bighead carp ( Hypophthalmichthys nobilis ) is a key aquaculture species, with the head and its orbital fat being a commercially valuable product. To elucidate the molecular basis of growth variation, we performed comparative transcriptome analysis of orbital fat from extreme growth phenotypes at juvenile (6 months) and market-size (18 months) stages. In juveniles, slow growth was linked to upregulation of stress-responsive genes ( sgk1 , fkbp5 , lipg ), while fast growth correlated with higher expression of stress-buffering ( crhbp ) and nutrient-signaling ( rbp2 , mgea5 ) genes. At 18 months, divergent growth aligned with opposing lipid metabolic states: a pro-anabolic profile ( dgat2 , fads2 ) supported fast growth, whereas a catabolic profile ( cpt1b , ppargc1a ) was associated with slow growth. These results demonstrate stage-specific transcriptional reprogramming in orbital fat underlying growth variation. This study provides a molecular framework for orbital fat-mediated growth regulation and highlights potential candidate genes for molecular breeding in bighead carp.

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.
  • • This is preclinical work; animal or laboratory results cannot be applied to humans.

Evidence level

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

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