Canine hyper-sociability structural variants associated with altered three-dimensional chromatin state.

Autor: Tandon D; Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, USA. dtandon@princeton.edu., Kubinyi E; Department of Ethology, ELTE Eötvös Loránd University, Budapest, Hungary.; MTA-ELTE Lendület 'Momentum' Companion Animal Research Group, Budapest, Hungary.; ELTE NAP Canine Brain Research Group, Budapest, Hungary., Sándor S; MTA-ELTE Lendület 'Momentum' Companion Animal Research Group, Budapest, Hungary., Faughnan H; Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, USA., Miklósi Á; Department of Ethology, ELTE Eötvös Loránd University, Budapest, Hungary., vonHoldt BM; Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, USA. vonholdt@princeton.edu.
Jazyk: angličtina
Zdroj: BMC genomics [BMC Genomics] 2024 Aug 07; Vol. 25 (1), pp. 767. Date of Electronic Publication: 2024 Aug 07.
DOI: 10.1186/s12864-024-10614-6
Abstrakt: Strong selection on complex traits can lead to skewed trait means and reduced trait variability in populations. An example of this phenomenon can be evidenced in allele frequency changes and skewed trait distributions driven by persistent human-directed selective pressures in domesticated species. Dog domestication is linked to several genomic variants; however, the functional impacts of these variants may not always be straightforward when found in non-coding regions of the genome. Four polymorphic transposable elements (TE) found within non-coding sites along a 5 Mb region on canine CFA6 have evolved due to directional selection associated with heightened human-directed hyper-sociability in domesticated dogs. We found that the polymorphic TE in intron 17 of the canine GTF2I gene, which was previously reported to be negatively correlated with canid human-directed hyper-sociability, is associated with altered chromatin looping and hence distinct cis-regulatory landscapes. We reported supporting evidence of an E2F1-DNA binding peak concordant with the altered loop and higher expression of GTF2I exon 18, indicative of alternative splicing. Globally, we discovered differences in pathways regulating the extra-cellular matrix with respect to TE copy number. Overall, we reported evidence suggesting an intriguing molecular convergence between the emergence of hypersocial behaviors in dogs and the same genes that, when hemizygous, produce human Williams Beuren Syndrome characterized by cranio-facial defects and heightened social behaviors. Our results additionally emphasize the often-overlooked potential role of chromatin architecture in social evolution.
(© 2024. The Author(s).)
Databáze: MEDLINE
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