In silico design of DNA sequences for in vivo nucleosome positioning

Author:

Routhier Etienne1,Joubert Alexandra2,Westbrook Alex2,Pierre Edgard1,Lancrey Astrid2,Cariou Marie3,Boulé Jean-Baptiste2ORCID,Mozziconacci Julien1234ORCID

Affiliation:

1. Laboratoire de Physique Théorique, CNRS, Sorbonne Université, Paris, France de la Matière Condensée, CNRS, Sorbonne Université , Paris, France

2. Structure et Instabilité des Génomes, Museum National d’Histoire Naturelle, CNRS , INSERM, Paris, France

3. Acquisition et Analyse de données pour l’histoire naturelle, Museum National d’Histoire Naturelle, CNRS , Paris, France

4. Institut Universitaire de France , Paris, France

Abstract

Abstract The computational design of synthetic DNA sequences with designer in vivo properties is gaining traction in the field of synthetic genomics. We propose here a computational method which combines a kinetic Monte Carlo framework with a deep mutational screening based on deep learning predictions. We apply our method to build regular nucleosome arrays with tailored nucleosomal repeat lengths (NRL) in yeast. Our design was validated in vivo by successfully engineering and integrating thousands of kilobases long tandem arrays of computationally optimized sequences which could accommodate NRLs much larger than the yeast natural NRL (namely 197 and 237 bp, compared to the natural NRL of ∼165 bp). RNA-seq results show that transcription of the arrays can occur but is not driven by the NRL. The computational method proposed here delineates the key sequence rules for nucleosome positioning in yeast and should be easily applicable to other sequence properties and other genomes.

Funder

Agence Nationale de la Recherche

Publisher

Oxford University Press (OUP)

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