Genome ResearchGenomicsPeer-reviewed journal article
CGC1, a new reference genome for Caenorhabditis elegans
Kazuki IchikawaiD, Massa J. ShouraiD, Karen L. ArtilesiD, Dae‐Eun JeongiD, Chie OwaiD, Haruka Kobayashi, Yoshihiko SuzukiiD, Manami Kanamori, Yu ToyoshimaiD, Yuichi IinoiD, Ann E. RougvieiD, Lamia WahbaiD, Andrew Z. FireiD, Erich M. SchwarziD, Shinichi MorishitaiD
Abstract
The original 100.3 Mb reference genome for Caenorhabditis elegans, generated from the wild-type laboratory strain N2, has been crucial for analysis of C. elegans since 1998 and has been considered complete since 2005. Unexpectedly, this long-standing reference was shown to be incomplete in 2019 by a genome assembly from the N2-derived strain VC2010. Moreover, genetically divergent versions of N2 have arisen over decades of research and hindered reproducibility of C. elegans genetics and genomics. Here we provide a 106.4 Mb gap-free, telomere-to-telomere genome assembly of C. elegans, generated from CGC1, an isogenic derivative of the N2 strain. We used improved long-read sequencing and manual assembly of 43 recalcitrant genomic regions to overcome deficiencies of prior N2 and VC2010 assemblies, and to assemble tandem repeat loci including a 772-kb sequence for the 45S rRNA genes. While many differences from earlier assemblies came from repeat regions, unique additions to the genome were also found. Of 19,972 protein-coding genes in the N2 assembly, 19,790 (99.1%) encode products that are unchanged in the CGC1 assembly. The CGC1 assembly also may encode 183 new protein-coding and 163 new ncRNA genes. CGC1 thus provides both a completely defined reference genome and corresponding isogenic wild-type strain for C. elegans, allowing unique opportunities for model and systems biology.
- organism: C. elegans
- assay: whole-genome sequencing
- research focus: database / resource
- approach: experimental assay
- Citations
- 11
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