Integrative characterization of G-Quadruplexes in the three-dimensional chromatin structure

Epigenetics. 2019 Sep;14(9):894-911. doi: 10.1080/15592294.2019.1621140. Epub 2019 Jun 10.

Abstract

DNA molecules are highly compacted in the eukaryotic nucleus where distal regulatory elements reach their targets through three-dimensional chromosomal interactions. G-quadruplexes, stable four-stranded non-canonical DNA structures, can change local chromatin organization through the exclusion of nucleosomes. However, the relationship between G-quadruplexes and higher-order genome organization remains unknown. Here, we found that G-quadruplexes are significantly enriched at boundaries of topological associated domains (TADs). Architectural protein occupancy, which plays critical roles in the formation of TADs, was highly correlated with the content of G-quadruplexes at TAD boundaries. Moreover, adjacent boundaries containing G-quadruplexes frequently interacted with each other because of the high enrichment of architectural protein binding sites. Similar to CCCTC-binding factor (CTCF) binding sites, G-quadruplexes also showed strong insulation ability in the separation of adjacent regions. Additionally, the insulation ability of CTCF binding sites and TAD boundaries was significantly reinforced by G-quadruplexes. Furthermore, G-quadruplex motifs on different strands were associated with the orientation of CTCF binding sites. These findings suggest a potential role for G-quadruplexes in loop extrusion. The enrichment of transcription factor binding sites (TFBSs) around regulatory elements containing G-quadruplexes led to frequent interactions between regulatory elements containing G-quadruplexes. Intriguingly, more than 99% of G-quadruplexes overlapped with TFBSs. The binding sites of CTCF and cohesin proteins were preferentially located surrounding G-quadruplexes. Accordingly, we proposed a new mechanism of long-distance gene regulation in which G-quadruplexes are involved in distal interactions between enhancers and promoters.

Keywords: Chromatin structure; G-quadruplex; Hi-C; enhancer-promoter interaction; loop extrusion; transcription factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • CCCTC-Binding Factor / metabolism*
  • Cell Cycle Proteins / metabolism*
  • Chromatin / chemistry*
  • Chromatin / metabolism*
  • Chromatin Immunoprecipitation Sequencing
  • Chromosomal Proteins, Non-Histone / metabolism*
  • Cohesins
  • DNA / chemistry
  • DNA / metabolism
  • Enhancer Elements, Genetic
  • G-Quadruplexes
  • Gene Expression Regulation
  • Humans
  • K562 Cells
  • Models, Molecular
  • Promoter Regions, Genetic
  • Sequence Analysis, RNA
  • Transcription Factors / metabolism*

Substances

  • CCCTC-Binding Factor
  • CTCF protein, human
  • Cell Cycle Proteins
  • Chromatin
  • Chromosomal Proteins, Non-Histone
  • Transcription Factors
  • DNA

Grants and funding

This work was supported by the National Natural Science Foundation of China under grant number 61472078; Key Research and Development Program of Jiangsu province under grant number BE2016002-3.