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Highly rearranged chromosomes reveal uncoupling between genome topology and gene expression.


ABSTRACT: Chromatin topology is intricately linked to gene expression, yet its functional requirement remains unclear. Here, we comprehensively assessed the interplay between genome topology and gene expression using highly rearranged chromosomes (balancers) spanning ~75% of the Drosophila genome. Using transheterozyte (balancer/wild-type) embryos, we measured allele-specific changes in topology and gene expression in cis, while minimizing trans effects. Through genome sequencing, we resolved eight large nested inversions, smaller inversions, duplications and thousands of deletions. These extensive rearrangements caused many changes to chromatin topology, disrupting long-range loops, topologically associating domains (TADs) and promoter interactions, yet these are not predictive of changes in expression. Gene expression is generally not altered around inversion breakpoints, indicating that mis-appropriate enhancer-promoter activation is a rare event. Similarly, shuffling or fusing TADs, changing intra-TAD connections and disrupting long-range inter-TAD loops does not alter expression for the majority of genes. Our results suggest that properties other than chromatin topology ensure productive enhancer-promoter interactions.

SUBMITTER: Ghavi-Helm Y 

PROVIDER: S-EPMC7116017 | biostudies-literature | 2019 Aug

REPOSITORIES: biostudies-literature

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Highly rearranged chromosomes reveal uncoupling between genome topology and gene expression.

Ghavi-Helm Yad Y   Jankowski Aleksander A   Meiers Sascha S   Viales Rebecca R RR   Korbel Jan O JO   Furlong Eileen E M EEM  

Nature genetics 20190715 8


Chromatin topology is intricately linked to gene expression, yet its functional requirement remains unclear. Here, we comprehensively assessed the interplay between genome topology and gene expression using highly rearranged chromosomes (balancers) spanning ~75% of the Drosophila genome. Using transheterozyte (balancer/wild-type) embryos, we measured allele-specific changes in topology and gene expression in cis, while minimizing trans effects. Through genome sequencing, we resolved eight large  ...[more]

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