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The axolotl genome and the evolution of key tissue formation regulators.
Nowoshilow, Sergej; Schloissnig, Siegfried; Fei, Ji-Feng; Dahl, Andreas; Pang, Andy W C; Pippel, Martin; Winkler, Sylke; Hastie, Alex R; Young, George; Roscito, Juliana G; Falcon, Francisco; Knapp, Dunja; Powell, Sean; Cruz, Alfredo; Cao, Han; Habermann, Bianca; Hiller, Michael; Tanaka, Elly M; Myers, Eugene W.
Afiliación
  • Nowoshilow S; Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
  • Schloissnig S; Research Institute of Molecular Pathology (IMP), Vienna Biocenter (VBC), Vienna, Austria.
  • Fei JF; DFG Research Center for Regenerative Therapies, Technische Universität Dresden, Dresden, Germany.
  • Dahl A; Heidelberg Institute for Theoretical Studies, Heidelberg, Germany.
  • Pang AWC; Institute for Brain Research and Rehabilitation, South China Normal University, Guangzhou, China.
  • Pippel M; DFG Research Center for Regenerative Therapies, Technische Universität Dresden, Dresden, Germany.
  • Winkler S; Deep Sequencing Group, Biotechnology Center (Biotec) Technische Universität Dresden, Dresden, Germany.
  • Hastie AR; Bionano Genomics, San Diego, California, USA.
  • Young G; Heidelberg Institute for Theoretical Studies, Heidelberg, Germany.
  • Roscito JG; Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
  • Falcon F; Bionano Genomics, San Diego, California, USA.
  • Knapp D; The Francis Crick Institute, London, UK.
  • Powell S; Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
  • Cruz A; Max Planck Institute for the Physics of Complex Systems, Dresden, Germany.
  • Cao H; Center for Systems Biology, Dresden, Germany.
  • Habermann B; Molecular and Developmental Complexity Group, Unidad de Genómica Avanzada, Langebio-Cinvestav, Irapuato, Mexico.
  • Hiller M; DFG Research Center for Regenerative Therapies, Technische Universität Dresden, Dresden, Germany.
  • Tanaka EM; Heidelberg Institute for Theoretical Studies, Heidelberg, Germany.
  • Myers EW; Molecular and Developmental Complexity Group, Unidad de Genómica Avanzada, Langebio-Cinvestav, Irapuato, Mexico.
Nature ; 554(7690): 50-55, 2018 02 01.
Article en En | MEDLINE | ID: mdl-29364872
ABSTRACT
Salamanders serve as important tetrapod models for developmental, regeneration and evolutionary studies. An extensive molecular toolkit makes the Mexican axolotl (Ambystoma mexicanum) a key representative salamander for molecular investigations. Here we report the sequencing and assembly of the 32-gigabase-pair axolotl genome using an approach that combined long-read sequencing, optical mapping and development of a new genome assembler (MARVEL). We observed a size expansion of introns and intergenic regions, largely attributable to multiplication of long terminal repeat retroelements. We provide evidence that intron size in developmental genes is under constraint and that species-restricted genes may contribute to limb regeneration. The axolotl genome assembly does not contain the essential developmental gene Pax3. However, mutation of the axolotl Pax3 paralogue Pax7 resulted in an axolotl phenotype that was similar to those seen in Pax3-/- and Pax7-/- mutant mice. The axolotl genome provides a rich biological resource for developmental and evolutionary studies.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Genoma / Evolución Molecular / Genómica / Ambystoma mexicanum Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Nature Año: 2018 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Genoma / Evolución Molecular / Genómica / Ambystoma mexicanum Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Nature Año: 2018 Tipo del documento: Article País de afiliación: Alemania