Recompleting the Caenorhabditis elegans genome

被引:73
|
作者
Yoshimura, Jun [1 ]
Ichikawa, Kazuki [1 ]
Shoura, Massa J. [2 ]
Artiles, Karen L. [2 ]
Gabdank, Idan [3 ]
Wahba, Lamia [2 ]
Smith, Cheryl L. [2 ,3 ]
Edgley, Mark L. [4 ,5 ]
Rougvie, Ann E. [6 ]
Fire, Andrew Z. [2 ,3 ]
Morishita, Shinichi [1 ]
Schwarz, Erich M. [7 ]
机构
[1] Univ Tokyo, Grad Sch Frontier Sci, Dept Computat Biol & Med Sci, Chiba 2778583, Japan
[2] Stanford Univ, Dept Pathol, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Genet, Stanford, CA 94305 USA
[4] Univ British Columbia, Dept Zool, Vancouver, BC V6T 1Z3, Canada
[5] Univ British Columbia, Michael Smith Labs, Vancouver, BC V6T 1Z3, Canada
[6] Univ Minnesota, Dept Genet Cell Biol & Dev, Minneapolis, MN 55454 USA
[7] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
C-ELEGANS; DNA; RNA; PREDICTION; EVOLUTION; SEQUENCE; PROTEIN; COMPLEXITY; SOFTWARE; DATABASE;
D O I
10.1101/gr.244830.118
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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; more-over, we predicted >= 53 new genes in VC2010. The recompleted genome of C. elegans should be a valuable resource for genetics, genomics, and systems biology.
引用
收藏
页码:1009 / 1022
页数:14
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