Stochastic motion and transcriptional dynamics of pairs of distal DNA loci on a compacted chromosome

Author:

Brückner David B.1ORCID,Chen Hongtao23ORCID,Barinov Lev34ORCID,Zoller Benjamin56ORCID,Gregor Thomas356ORCID

Affiliation:

1. Institute of Science and Technology, Am Campus 1, Klosterneuburg, Austria.

2. School of Life Science and Technology, ShanghaiTech University, Shanghai, China.

3. Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA.

4. Memorial Sloan Kettering Cancer Center, New York, NY, USA.

5. Joseph Henry Laboratories of Physics, Princeton University, Princeton, NJ, USA.

6. Department of Developmental and Stem Cell Biology, CNRS UMR3738 Paris Cité, Institut Pasteur, Paris, France.

Abstract

Chromosomes in the eukaryotic nucleus are highly compacted. However, for many functional processes, including transcription initiation, the pairwise motion of distal chromosomal elements such as enhancers and promoters is essential and necessitates dynamic fluidity. Here, we used a live-imaging assay to simultaneously measure the positions of pairs of enhancers and promoters and their transcriptional output while systematically varying the genomic separation between these two DNA loci. Our analysis reveals the coexistence of a compact globular organization and fast subdiffusive dynamics. These combined features cause an anomalous scaling of polymer relaxation times with genomic separation leading to long-ranged correlations. Thus, encounter times of DNA loci are much less dependent on genomic distance than predicted by existing polymer models, with potential consequences for eukaryotic gene expression.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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