A comparative analysis of planarian genomes reveals regulatory conservation in the face of rapid structural divergence

Mario Ivanković(Max Planck Institute for Dynamics and Self-Organization), Jeremias N. Brand(Max Planck Institute for Dynamics and Self-Organization), Luca Pandolfini(Italian Institute of Technology), Tom Brown(Max Planck Institute of Molecular Cell Biology and Genetics), Martin Pippel(Max Planck Institute of Molecular Cell Biology and Genetics), Andrei Rozanski(Max Planck Institute for Dynamics and Self-Organization), Til Schubert(Max Planck Institute for Dynamics and Self-Organization), Markus A. Grohme(Max Planck Institute of Molecular Cell Biology and Genetics), Sylke Winkler(Max Planck Institute of Molecular Cell Biology and Genetics), Laura Ávila Robledillo(Max Planck Institute for Plant Breeding Research), Meng Zhang(Max Planck Institute for Plant Breeding Research), Azzurra Codino(Italian Institute of Technology), Stefano Gustincich(Italian Institute of Technology), Miquel Vila‐Farré(Max Planck Institute for Dynamics and Self-Organization), Shu Zhang(Universitätsmedizin Göttingen), Argyris Papantonis(Universitätsmedizin Göttingen), André Marques(Max Planck Institute for Plant Breeding Research), Jochen C. Rink(Max Planck Institute for Dynamics and Self-Organization)
Nature Communications
September 18, 2024
Cited by 36Open Access
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Abstract

The planarian Schmidtea mediterranea is being studied as a model species for regeneration, but the assembly of planarian genomes remains challenging. Here, we report a high-quality haplotype-phased, chromosome-scale genome assembly of the sexual S2 strain of S. mediterranea and high-quality chromosome-scale assemblies of its three close relatives, S. polychroa, S. nova, and S. lugubris. Using hybrid gene annotations and optimized ATAC-seq and ChIP-seq protocols for regulatory element annotation, we provide valuable genome resources for the planarian research community and a first comparative perspective on planarian genome evolution. Our analyses reveal substantial divergence in protein-coding sequences and regulatory regions but considerable conservation within promoter and enhancer annotations. We also find frequent retrotransposon-associated chromosomal inversions and interchromosomal translocations within the genus Schmidtea and, remarkably, independent and nearly complete losses of ancestral metazoan synteny in Schmidtea and two other flatworm groups. Overall, our results suggest that platyhelminth genomes can evolve without syntenic constraints.


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