Document Type

Article

Publication Date

12-1-2022

Keywords

JGM

JAX Source

Adv Genet (Hoboken). 2022;3(4):2100010.

ISSN

2641-6573

PMID

36911294

DOI

https://doi.org/10.1002/ggn2.202100010

Grant

L.L. is supported by the National Key Research and Development Pro- gram of China (Grant No. 2017YFA0205200), the National Natural Science Foundation of China (Grant No. 81901857, 81801811), Natural Science Foundation of Guangdong Province, China (Grant No. 2018A030313074). X.C. is supported by Shenzhen Science and Technology Foundation (GCZX2015043016165447).

Abstract

The fundamental cause of transcription dysregulation in hepatocellular carcinoma (HCC) remains elusive. To investigate the underlying mechanisms, comprehensive 3D-epigenomic analyses are performed in cellular models of THLE2 (a normal hepatocytes cell line) and HepG2 (a hepatocellular carcinoma cell line) using integrative approaches for chromatin topology, genomic and epigenomic variation, and transcriptional output. Comparing the 3D-epigenomes in THLE2 and HepG2 reveal that most HCC-associated genes are organized in complex chromatin interactions mediated by RNA polymerase II (RNAPII). Incorporation of genome-wide association studies (GWAS) data enables the identification of non-coding genetic variants that are enriched in distal enhancers connecting to the promoters of HCC-associated genes via long-range chromatin interactions, highlighting their functional roles. Interestingly, CTCF binding and looping proximal to HCC-associated genes appear to form chromatin architectures that overarch RNAPII-mediated chromatin interactions. It is further demonstrated that epigenetic variants by DNA hypomethylation at a subset of CTCF motifs proximal to HCC-associated genes can modify chromatin topological configuration, which in turn alter RNAPII-mediated chromatin interactions and lead to dysregulation of transcription. Together, the 3D-epigenomic analyses provide novel insights of multifaceted interplays involving genetics, epigenetics, and chromatin topology in HCC cells.

Comments

This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

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