Your browser doesn't support javascript.
loading
Recompleting the Caenorhabditis elegans genome.
Yoshimura, Jun; Ichikawa, Kazuki; Shoura, Massa J; Artiles, Karen L; Gabdank, Idan; Wahba, Lamia; Smith, Cheryl L; Edgley, Mark L; Rougvie, Ann E; Fire, Andrew Z; Morishita, Shinichi; Schwarz, Erich M.
Afiliación
  • Yoshimura J; Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Chiba 277-8583, Japan.
  • Ichikawa K; Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Chiba 277-8583, Japan.
  • Shoura MJ; Department of Pathology, Stanford University, Stanford, California 94305, USA.
  • Artiles KL; Department of Pathology, Stanford University, Stanford, California 94305, USA.
  • Gabdank I; Department of Genetics, Stanford University, Stanford, California 94305, USA.
  • Wahba L; Department of Pathology, Stanford University, Stanford, California 94305, USA.
  • Smith CL; Department of Pathology, Stanford University, Stanford, California 94305, USA.
  • Edgley ML; Department of Genetics, Stanford University, Stanford, California 94305, USA.
  • Rougvie AE; Department of Zoology and Michael Smith Laboratories, University of British Columbia, Vancouver V6T 1Z3, British Columbia, Canada.
  • Fire AZ; Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, Minnesota 55454, USA.
  • Morishita S; Department of Pathology, Stanford University, Stanford, California 94305, USA.
  • Schwarz EM; Department of Genetics, Stanford University, Stanford, California 94305, USA.
Genome Res ; 29(6): 1009-1022, 2019 06.
Article en En | MEDLINE | ID: mdl-31123080
ABSTRACT
Caenorhabditis elegans was the first multicellular eukaryotic genome sequenced to apparent completion. Although this assembly employed a standard C. elegans strain (N2), it used sequence data from several laboratories, with DNA propagated in bacteria and yeast. Thus, the N2 assembly has many differences from any C. elegans available today. To provide a more accurate C. elegans genome, we performed long-read assembly of VC2010, a modern strain derived from N2. Our VC2010 assembly has 99.98% identity to N2 but with an additional 1.8 Mb including tandem repeat expansions and genome duplications. For 116 structural discrepancies between N2 and VC2010, 97 structures matching VC2010 (84%) were also found in two outgroup strains, implying deficiencies in N2. Over 98% of N2 genes encoded unchanged products in VC2010; moreover, we predicted ≥53 new genes in VC2010. The recompleted genome of C. elegans should be a valuable resource for genetics, genomics, and systems biology.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Caenorhabditis elegans / Genómica / Genoma de los Helmintos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Genome Res Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA Año: 2019 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Caenorhabditis elegans / Genómica / Genoma de los Helmintos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Genome Res Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA Año: 2019 Tipo del documento: Article País de afiliación: Japón