Abstract

Numerous intra- and inter-chromosomal contacts have been mapped in eukaryotic genomes, but it remains challenging to link these 3D structures to their regulatory functions. To establish the causal relationships between chromosome conformation and genome functions, we develop a method, Chemically Induced Chromosomal Interaction (CICI), to selectively perturb the chromosome conformation at targeted loci. Using this method, long-distance chromosomal interactions can be induced dynamically between intra- or inter-chromosomal loci pairs, including the ones with very low Hi-C contact frequencies. Measurement of CICI formation time allows us to probe chromosome encounter dynamics between different loci pairs across the cell cycle. We also conduct two functional tests of CICI. We perturb the chromosome conformation near a DNA double-strand break and observe altered donor preference in homologous recombination; we force interactions between early and late-firing DNA replication origins and find no significant changes in replication timing. These results suggest that chromosome conformation plays a deterministic role in homology-directed DNA repair, but not in the establishment of replication timing. Overall, our study demonstrates that CICI is a powerful tool to study chromosome dynamics and 3D genome function.

Highlights

  • Numerous intra- and inter-chromosomal contacts have been mapped in eukaryotic genomes, but it remains challenging to link these 3D structures to their regulatory functions

  • Note that if we use LacI-FKBP12-GFP and TetR-FKBP-rapamycin binding domain (FRB)-mCherry triple fusions, co-localized chromatin dots may represent two chromatin loci bound together as intended by Chromosomal Interactions (CICI), or chromatin-bound FKBP12/FRB associated with free FRB/FKBP12

  • We developed a synthetic biology method, CICI, to induce chromosomal interactions between targeted loci

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Summary

Introduction

Numerous intra- and inter-chromosomal contacts have been mapped in eukaryotic genomes, but it remains challenging to link these 3D structures to their regulatory functions. We (1) develop a method that can rapidly induce chromosomal interactions between different pairs of targeted loci, including ones with very low contact frequency, (2) measure the rate and efficiency of Chemically Induced Chromosomal Interactions (CICI) formation, and investigate their relations to the Hi-C contact frequencies of the targeted loci pair, (3) use time-lapse assay to monitor CICI formation and disruption in single cells in real time, and evaluate the dynamics of these events at different cell cycle stages, (4) perturb the chromosome conformation near a DNA double-stranded break and probe its impact on DNA repair, and (5) force interactions between early and late-firing replication origins and measure the resulting DNA replication timing These studies demonstrate that CICI is a powerful tool to study chromosome dynamics and 3D genome functions

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