Dynamic chromatin architecture of the porcine adipose tissues with weight gain and loss
Nature Communications · 34 authors, 12 centres
AI SUMMARY
FIDELITY 100%
POPULATIONAdult female miniature pigs with diet-induced weight gain or weight loss
INTERVENTIONDietary intervention leading to weight gain or weight loss over 12 weeks
COMPARISONComparisons between subcutaneous adipose tissue (SAT) and visceral adipose tissues (VATs), and between weight gain and weight loss groups
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Using a pig model, this study generated high-resolution chromatin contact maps to show that 3D genome architecture remodeling underlies transcriptomic differences between subcutaneous and visceral adipose tissues during weight gain and loss, providing a resource for identifying obesity-related regulatory elements.
Full summary
1,035 CHARS
This preclinical study used adult female miniature pigs to investigate diet-induced changes in the 3D genome architecture of subcutaneous and visceral adipose tissues. The researchers generated 249 high-resolution in situ Hi-C maps to analyze chromatin contact patterns alongside transcriptomic data. The central finding is that remodeling of chromatin architecture, including changes in A/B compartments and TAD boundaries, underpins transcriptomic divergence between anatomically distinct fat depots, potentially linked to metabolic risks. The study also performed comparative analyses, finding similarities in obesity-related regulatory elements between pigs and humans, as well as species-specific elements. A key limitation is the use of bulk Hi-C, which provides average chromatin features and does not resolve cellular heterogeneity. The implications suggest the pig model is valuable for studying human obesity and that the generated data can serve as a resource for linking obesity-associated genetic variants to target genes.
PICO
PPOPULATION
Adult female miniature pigs with diet-induced weight gain or weight loss
IINTERVENTION
Dietary intervention leading to weight gain or weight loss over 12 weeks
OOUTCOME
Changes in 3D chromatin architecture (A/B compartments, TADs) and transcriptomic profiles in adipose tissues