A chromosome-level genome assembly of a model conifer plant, the Japanese cedar, Cryptomeria japonica D. Don

被引:8
作者
Fujino, Takeshi [1 ]
Yamaguchi, Katsushi [2 ]
Yokoyama, Toshiyuki T. [1 ]
Hamanaka, Toshiya [1 ]
Harazono, Yoritaka [1 ]
Kamada, Hiroaki [1 ]
Kobayashi, Wataru [1 ]
Ujino-Ihara, Tokuko [3 ]
Uchiyama, Kentaro [3 ]
Matsumoto, Asako [3 ]
Izuno, Ayako [3 ]
Tsumura, Yoshihiko [4 ]
Toyoda, Atsushi [5 ]
Shigenobu, Shuji [2 ]
Moriguchi, Yoshinari [6 ]
Ueno, Saneyoshi [3 ]
Kasahara, Masahiro [1 ]
机构
[1] Univ Tokyo, Grad Sch Frontier Sci, Kashiwa 2778561, Japan
[2] Natl Inst Basic Biol, Transscale Biol Ctr, Okazaki 4448585, Japan
[3] Forestry & Forest Prod Res Inst, Dept Forest Mol Genet & Biotechnol, Tsukuba 3058687, Japan
[4] Univ Tsukuba, Fac Life & Environm Sci, Tsukuba 3058572, Japan
[5] Natl Inst Genet, Comparat Genom Lab, Mishima 4118540, Japan
[6] Niigata Univ, Fac Agr, Niigata 9502181, Japan
关键词
Cryptomeria japonica; Sugi; Genome assembly; HiFi sequencing; Hi-C scaffolding; Gene annotation; Repetitive elements; Model conifer; SEQUENCE; EVOLUTIONARY; GENE; VISUALIZATION; REGENERATION; CONVERSION; ALIGNMENT; DATABASE; PROVIDES; UPDATE;
D O I
10.1186/s12864-024-10929-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background The Japanese cedar (Cryptomeria japonica D. Don) is one of the most important Japanese forest trees, occupying approximately 44% of artificial forests and planted in East Asia, the Azores Archipelago, and certain islands in the Indian Ocean. Although the huge genome of the species (ca. 9 Gbp) with abundant repeat elements may have represented an obstacle for genetic analysis, this species is easily propagated by cutting, flowered by gibberellic acid, transformed by Agrobacterium, and edited by CRISPR/Cas9. These characteristics of C. japonica recommend it as a model conifer species for which reference genome sequences are necessary. Results Herein, we report the first chromosome-level assembly of C. japonica (2n = 22) using third-generation selfed progeny (estimated homozygosity rate = 0.96). Young leaf tissue was used to extract high molecular weight DNA (> 50 kb) for HiFi PacBio long-read sequencing and to construct an Hi-C/Omni-C library for Illumina short-read sequencing. The 29x and 26x genome coverage of HiFi and Illumina reads, respectively, for de novo assembly yielded 2,651 contigs (9.1 Gbp, N50 contig size 12.0 Mbp). Hi-C analysis mapped 97% of the nucleotides on 11 chromosomes. The assembly was verified through comparison with a consensus linkage map comprising 7,781 markers. BUSCO analysis identified similar to 91% conserved genes. Conclusions Annotations of genes and comparisons of repeat elements with other Cupressaceae and Pinaceae species provide a fundamental resource for conifer research.
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页数:16
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