Evolutionary divergence in CTCF-mediated chromatin topology drives transcriptional innovation in humans

Chromatin topology can impact gene regulation, but how evolutionary divergence in chromatin topology has shaped gene regulatory landscapes for distinctive human traits remains poorly understood. CTCF sites determine chromatin topology by forming domains and loops. Here, we show evolutionary divergence in CTCF-mediated chromatin topology at the domain and loop scales during primate evolution, elucidating distinct mechanisms for shaping regulatory landscapes. Human-specific divergent domains lead to a broad rewiring of transcriptional landscapes. Divergent CTCF loops concord with species-specific enhancer activity, influencing enhancer connectivity to target genes in a concordant yet constrained manner. Under this concordant mechanism, we establish the role of human-specific CTCF loops in shaping transcriptional isoform diversity, with functional implications for disease susceptibility. Furthermore, we validate the function of these human-specific CTCF loops using human forebrain organoids. This study advances our understanding of genetic evolution from the perspective of genome architecture.

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Publication Details

Journal
Nature Communications
Published
2025-03-26
DOI
https://doi.org/10.1038/s41467-025-58275-7
Citations
4
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
3.22

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article

Evolutionary divergence in CTCF-mediated chromatin topology drives transcriptional innovation in humans

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4 citations
Nature Communications
Genomics and Chromatin Dynamics
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article

Evolutionary divergence in CTCF-mediated chromatin topology drives transcriptional innovation in humans

Xinyu Gao, Xia Wu, Wen‐Jun Xin, Dariusz Plewczyński, Yuhan Tian, Dan Xiong, Fang Fu, Xin Yang, Jingjing Duan, Andy Peng Xiang, Xinlai Cheng, Zhonghui Tang, Ting Xu, Minji Kim, Li Chen, Wei Dong, Rong Liu, Lanqi Hu, Xingqiang Lai, Ziying Xie, Tianyun Wang, Xian Zeng
article en
4 citations

Abstract

Chromatin topology can impact gene regulation, but how evolutionary divergence in chromatin topology has shaped gene regulatory landscapes for distinctive human traits remains poorly understood. CTCF sites determine chromatin topology by forming domains and loops. Here, we show evolutionary divergence in CTCF-mediated chromatin topology at the domain and loop scales during primate evolution, elucidating distinct mechanisms for shaping regulatory landscapes. Human-specific divergent domains lead to a broad rewiring of transcriptional landscapes. Divergent CTCF loops concord with species-specific enhancer activity, influencing enhancer connectivity to target genes in a concordant yet constrained manner. Under this concordant mechanism, we establish the role of human-specific CTCF loops in shaping transcriptional isoform diversity, with functional implications for disease susceptibility. Furthermore, we validate the function of these human-specific CTCF loops using human forebrain organoids. This study advances our understanding of genetic evolution from the perspective of genome architecture.

Nature CommunicationsVol. 16(1)
Warsaw University of Technology (PL), Goethe University Frankfurt (DE), Sun Yat-sen University (CN), Peking University (CN), National Health and Family Planning Commission (CN), University of Michigan (US), The First Affiliated Hospital, Sun Yat-sen University (CN), Frankfurt Cancer Institute (DE), University of Warsaw (PL), Guangzhou Medical University (CN)
National Natural Science Foundation of China
Industry, innovation and infrastructure
Openalex Percentile: Top 9%
Genomics and Chromatin Dynamics
3.22
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