A chromosome-level genome assembly of wild silkmoth, Bombyx mandarina

被引:0
|
作者
Lee, Jung [1 ]
Kiuchi, Takashi [2 ]
Yamaguchi, Katsushi [3 ]
Shigenobu, Shuji [3 ]
Toyoda, Atsushi [4 ]
Shimada, Toru [1 ,2 ]
机构
[1] Gakushuin Univ, Fac Sci, Dept Life Sci, Mejiro 1-5-1,Toshima Ku, Tokyo 1718588, Japan
[2] Univ Tokyo, Grad Sch Agr & Life Sci, Bunkyo Ku, Tokyo 1138657, Japan
[3] Natl Inst Basic Biol, Transom Facil, Nishigonaka 38, Myodaiji, Okazaki 4448585, Japan
[4] Natl Inst Genet, Adv Genom Ctr, Comparat Genom Lab, 1111 Yata, Mishima, Shizuoka 4118540, Japan
基金
日本学术振兴会;
关键词
D O I
10.1038/s41597-025-04395-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The wild silk moth, Bombyx mandarina, is the closest relative of the domesticated silk moth, Bombyx mori. National BioResource Project of Japan (NBRP) maintains a B. mandarina strain derived from individuals captured at Sakado (Saitama, Japan) in 1982. Now, NBRP has developed chromosome replacement strains of B. mori. In each strain, one autosome of B. mori was replaced with the corresponding chromosome of B. mandarina. To facilitate the use of chromosome replacement strains and B. mandarina itself, we constructed a chromosome-level genome assembly of B. mandarina. Furthermore, we performed functional annotations of the genome assembly, i.e., transcriptome-based gene prediction, Assay for Transposase-Accessible Chromatin (ATAC)-seq, and PIWI-interacting RNA (piRNA)-targeted small RNA-seq. The assembly harbors 14,859 protein-coding genes and 628 piRNA clusters across three tissues: ovaries, testis, and embryos. ATAC-seq data comprehensively detected open chromosome regions, which will benefit when CRISPR/Cas9-mediated genome editing is conducted.
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页数:9
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