The genome of Schmidtea mediterranea and the evolution of core cellular mechanisms

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Markus Alexander Grohme - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Siegfried Schloissnig - , Heidelberg Institute for Theoretical Studies (Author)
  • Andrei Rozanski - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Martin Pippel - , Heidelberg Institute for Theoretical Studies (Author)
  • George Robert Young - , The Francis Crick Institute (Author)
  • Sylke Winkler - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Holger Brandl - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Ian Henry - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Andreas Dahl - , Center for Regenerative Therapies Dresden (Author)
  • Sean Powell - , Heidelberg Institute for Theoretical Studies (Author)
  • Michael Hiller - , Max Planck Institute of Molecular Cell Biology and Genetics, Max-Planck-Institute for the Physics of Complex Systems (Author)
  • Eugene Myers - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Jochen Christian Rink - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)

Abstract

The planarian Schmidtea mediterranea is an important model for stem cell research and regeneration, but adequate genome resources for this species have been lacking. Here we report a highly contiguous genome assembly of S. mediterranea, using long-read sequencing and a de novo assembler (MARVEL) enhanced for low-complexity reads. The S. mediterranea genome is highly polymorphic and repetitive, and harbours a novel class of giant retroelements. Furthermore, the genome assembly lacks a number of highly conserved genes, including critical components of the mitotic spindle assembly checkpoint, but planarians maintain checkpoint function. Our genome assembly provides a key model system resource that will be useful for studying regeneration and the evolutionary plasticity of core cell biological mechanisms.

Details

Original languageEnglish
Pages (from-to)56-61
Number of pages6
JournalNature
Volume554
Issue number7690
Publication statusPublished - 1 Feb 2018
Peer-reviewedYes

External IDs

PubMed 29364871
ORCID /0000-0002-8134-5929/work/142257683

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