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Inter3D:捕获 TAD 重排赋予基因转录的变体模式。

Inter3D: Capture of TAD Reorganization Endows Variant Patterns of Gene Transcription.

机构信息

State Key Laboratory of Cardiology and Medical Innovation Center, Institute for Regenerative Medicine, Shanghai East Hospital, Frontier Science Research Center for Stem Cells, School of Life Science and Technology, Tongji University, Shanghai 200092, China.

Jiangxi Province Key Laboratory of Organ Development and Epigenetics, Clinical Medical Research Center, Affiliated Hospital of Jinggangshan University, Medical Department of Jinggangshan University, Ji'an 343009, China.

出版信息

Genomics Proteomics Bioinformatics. 2024 Sep 13;22(3). doi: 10.1093/gpbjnl/qzae034.

Abstract

Topologically associating domain (TAD) reorganization commonly occurs in the cell nucleus and contributes to gene activation and inhibition through the separation or fusion of adjacent TADs. However, functional genes impacted by TAD alteration and the underlying mechanism of TAD reorganization regulating gene transcription remain to be fully elucidated. Here, we first developed a novel approach termed Inter3D to specifically identify genes regulated by TAD reorganization. Our study revealed that the segregation of TADs led to the disruption of intrachromosomal looping at the myosin light chain 12B (MYL12B) locus, via the meticulous reorganization of TADs mediating epigenomic landscapes within tumor cells, thereby exhibiting a significant correlation with the down-regulation of its transcriptional activity. Conversely, the fusion of TADs facilitated intrachromosomal interactions, suggesting a potential association with the activation of cytochrome P450 family 27 subfamily B member 1 (CYP27B1). Our study provides comprehensive insight into the capture of TAD rearrangement-mediated gene loci and moves toward understanding the functional role of TAD reorganization in gene transcription. The Inter3D pipeline developed in this study is freely available at https://github.com/bm2-lab/inter3D and https://ngdc.cncb.ac.cn/biocode/tool/BT7399.

摘要

拓扑关联域(TAD)重排通常发生在细胞核中,并通过相邻 TAD 的分离或融合来促进基因的激活和抑制。然而,TAD 改变所影响的功能基因以及调节基因转录的 TAD 重排的潜在机制仍有待充分阐明。在这里,我们首先开发了一种称为 Inter3D 的新方法,专门用于识别受 TAD 重排调节的基因。我们的研究表明,TAD 的分离导致肌球蛋白轻链 12B(MYL12B)基因座上的染色体内环断裂,这是通过肿瘤细胞内染色质构象景观的 TAD 介导的细致重排实现的,因此与其转录活性的下调显著相关。相反,TAD 的融合促进了染色体内相互作用,提示其与细胞色素 P450 家族 27 亚家族 B 成员 1(CYP27B1)的激活有关。我们的研究提供了对 TAD 重排介导的基因座捕获的全面了解,并有助于理解 TAD 重排在基因转录中的功能作用。本研究中开发的 Inter3D 流程可在 https://github.com/bm2-lab/inter3Dhttps://ngdc.cncb.ac.cn/biocode/tool/BT7399 上免费获取。

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