Abstract
ABSTRACT Despite the prominence of laboratory rats in behavioral neuroscience and complex trait genetics, a significant gap exists in the functional rat genomics database that explains the regulation of gene expression at the genome level. To address this, we analyzed genome-wide Hi-C data from the frontal cortex of ten strains in the Hybrid Rat Diversity Panel. While originally generated to improve the rat genome assembly, these data provided a unique opportunity to characterize the regulatory landscape of the adult rat brain. We identified an average of 5,899 ± 1,997 (STD) loops per sample and integrated these with over 3 million curated CTCF binding sites, which serve as architectural anchors for chromatin loops. Our multi-stage filtering workflow identified 15,085 unique, high-confidence regulatory interactions throughout the genome. As a validation of our approach, we observed that genes with the highest loop counts, including Foxo1, Gja1 , and Spry2 , were significantly enriched for developmental processes, reflecting the role of 3D genome structure in maintaining adult neuronal identity. The resulting resource addresses a critical deficiency in rat functional genomics and provides a foundation for dissecting the genetic architecture of complex traits.
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ABSTRACT
Despite the prominence of laboratory rats in behavioral neuroscience and complex trait genetics, a significant gap exists in the functional rat genomics database that explains the regulation of gene expression at the genome level. To address this, we analyzed genome-wide Hi-C data from the frontal cortex of ten strains in the Hybrid Rat Diversity Panel. While originally generated to improve the rat genome assembly, these data provided a unique opportunity to characterize the regulatory landscape of the adult rat brain. We identified an average of 5,899 ± 1,997 (STD) loops per sample and integrated these with over 3 million curated CTCF binding sites, which serve as architectural anchors for chromatin loops. Our multi-stage filtering workflow identified 15,085 unique, high-confidence regulatory interactions throughout the genome. As a validation of our approach, we observed that genes with the highest loop counts, including Foxo1, Gja1, and Spry2, were significantly enriched for developmental processes, reflecting the role of 3D genome structure in maintaining adult neuronal identity. The resulting resource addresses a critical deficiency in rat functional genomics and provides a foundation for dissecting the genetic architecture of complex traits.
Competing Interest Statement
The authors have declared no competing interest.
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