Abstract

The classic model of eukaryotic gene expression requires direct spatial contact between a distal enhancer and a proximal promoter. Recent Chromosome Conformation Capture (3C) studies show that enhancers and promoters are embedded in a complex network of looping interactions. Here we use a polymer model of chromatin fiber to investigate whether, and to what extent, looping interactions between elements in the vicinity of an enhancer-promoter pair can influence their contact frequency. Our equilibrium polymer simulations show that a chromatin loop, formed by elements flanking either an enhancer or a promoter, suppresses enhancer-promoter interactions, working as an insulator. A loop formed by elements located in the region between an enhancer and a promoter, on the contrary, facilitates their interactions. We find that different mechanisms underlie insulation and facilitation; insulation occurs due to steric exclusion by the loop, and is a global effect, while facilitation occurs due to an effective shortening of the enhancer-promoter genomic distance, and is a local effect. Consistently, we find that these effects manifest quite differently for in silico 3C and microscopy. Our results show that looping interactions that do not directly involve an enhancer-promoter pair can nevertheless significantly modulate their interactions. This phenomenon is analogous to allosteric regulation in proteins, where a conformational change triggered by binding of a regulatory molecule to one site affects the state of another site.

Highlights

  • Distal enhancer elements in higher eukaryotes are essential for regulating gene expression [1,2,3,4]

  • We model a region of chromatin fiber as a long polymer and study how the formation of loops between certain regulatory elements can insulate or facilitate enhancer-promoter interactions

  • Our findings suggest that loop-mediated gene regulation by elements in the vicinity of an enhancer-promoter pair can be understood as an allosteric effect

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Summary

Introduction

Distal enhancer elements in higher eukaryotes are essential for regulating gene expression [1,2,3,4]. Gene expression and E-P interactions occur within higher-order threedimensional chromatin organization, which is characterized by an intricate network of interactions at multiple scales. Below 1 Mb, chromatin is organized into continuous 500–900 kb regions of enriched contact frequency called topologically associated domains (TADs) [9,10]. Within TADs, additional cell-type specific looping interactions are formed [6,11,12]. These observations raise an important question; namely, how can E-P contacts be affected by looping interactions between other regulatory elements in their genomic neighborhood?

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