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The hagfish genome and the evolution of vertebrates.
Marlétaz, Ferdinand; Timoshevskaya, Nataliya; Timoshevskiy, Vladimir A; Parey, Elise; Simakov, Oleg; Gavriouchkina, Daria; Suzuki, Masakazu; Kubokawa, Kaoru; Brenner, Sydney; Smith, Jeramiah J; Rokhsar, Daniel S.
Afiliação
  • Marlétaz F; Centre for Life's Origins and Evolution, Department of Genetics, Evolution and Environment, University College London, London, UK. f.marletaz@ucl.ac.uk.
  • Timoshevskaya N; Molecular Genetics Unit, Okinawa Institute of Science and Technology Graduate University, Okinawa, Japan. f.marletaz@ucl.ac.uk.
  • Timoshevskiy VA; Department of Biology, University of Kentucky, Lexington, KY, USA.
  • Parey E; Department of Biology, University of Kentucky, Lexington, KY, USA.
  • Simakov O; Centre for Life's Origins and Evolution, Department of Genetics, Evolution and Environment, University College London, London, UK.
  • Gavriouchkina D; Molecular Genetics Unit, Okinawa Institute of Science and Technology Graduate University, Okinawa, Japan.
  • Suzuki M; Department for Neurosciences and Developmental Biology, University of Vienna, Vienna, Austria.
  • Kubokawa K; Molecular Genetics Unit, Okinawa Institute of Science and Technology Graduate University, Okinawa, Japan.
  • Brenner S; UK Dementia Research Institute, University College London, London, UK.
  • Smith JJ; Department of Science, Graduate School of Integrated Science and Technology, Shizuoka University, Shizuoka, Japan.
  • Rokhsar DS; Ocean Research Institute, The University of Tokyo, Tokyo, Japan.
Nature ; 627(8005): 811-820, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38262590
ABSTRACT
As the only surviving lineages of jawless fishes, hagfishes and lampreys provide a crucial window into early vertebrate evolution1-3. Here we investigate the complex history, timing and functional role of genome-wide duplications4-7 and programmed DNA elimination8,9 in vertebrates in the light of a chromosome-scale genome sequence for the brown hagfish Eptatretus atami. Combining evidence from syntenic and phylogenetic analyses, we establish a comprehensive picture of vertebrate genome evolution, including an auto-tetraploidization (1RV) that predates the early Cambrian cyclostome-gnathostome split, followed by a mid-late Cambrian allo-tetraploidization (2RJV) in gnathostomes and a prolonged Cambrian-Ordovician hexaploidization (2RCY) in cyclostomes. Subsequently, hagfishes underwent extensive genomic changes, with chromosomal fusions accompanied by the loss of genes that are essential for organ systems (for example, genes involved in the development of eyes and in the proliferation of osteoclasts); these changes account, in part, for the simplification of the hagfish body plan1,2. Finally, we characterize programmed DNA elimination in hagfish, identifying protein-coding genes and repetitive elements that are deleted from somatic cell lineages during early development. The elimination of these germline-specific genes provides a mechanism for resolving genetic conflict between soma and germline by repressing germline and pluripotency functions, paralleling findings in lampreys10,11. Reconstruction of the early genomic history of vertebrates provides a framework for further investigations of the evolution of cyclostomes and jawed vertebrates.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vertebrados / Evolução Molecular / Feiticeiras (Peixe) Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vertebrados / Evolução Molecular / Feiticeiras (Peixe) Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article