Draft Sequences of the Radish (Raphanus sativus L.) Genome

被引:136
|
作者
Kitashiba, Hiroyasu [1 ]
Li, Feng [1 ]
Hirakawa, Hideki [2 ]
Kawanabe, Takahiro [1 ]
Zou, Zhongwei [1 ]
Hasegawa, Yoichi [1 ]
Tonosaki, Kaoru [1 ]
Shirasawa, Sachiko [1 ]
Fukushima, Aki [1 ]
Yokoi, Shuji [3 ]
Takahata, Yoshihito [3 ]
Kakizaki, Tomohiro [4 ]
Ishida, Masahiko [4 ]
Okamoto, Shunsuke [5 ]
Sakamoto, Koji [5 ]
Shirasawa, Kenta [2 ]
Tabata, Satoshi [2 ]
Nishio, Takeshi [1 ]
机构
[1] Tohoku Univ, Grad Sch Agr Sci, Aoba Ku, Sendai, Miyagi 9818555, Japan
[2] Kazusa DNA Res Inst, Kisarazu, Chiba 2920818, Japan
[3] Iwate Univ, Fac Agr, Morioka, Iwate 0208550, Japan
[4] Natl Inst Vegetable & Tea Sci, Tsu, Mie 5142392, Japan
[5] Takii Seed Co Ltd, Plant Breeding Expt Stn, Kohsei, Shiga 52020, Japan
关键词
radish; draft sequence; high-density genetic map; NUCLEOTIDE-SEQUENCES; BRASSICA-RAPA; LINKAGE MAP; SNP MARKERS; DATABASE; GENE; DNA; IDENTIFICATION; EVOLUTION; PROTEIN;
D O I
10.1093/dnares/dsu014
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Radish (Raphanus sativus L., n = 5 9) is one of the major vegetables in Asia. Since the genomes of Brassica and related species including radish underwent genome rearrangement, it is quite difficult to perform functional analysis based on the reported genomic sequence of Brassica rapa. Therefore, we performed genome sequencing of radish. Short reads of genomic sequences of 191.1 Gb were obtained by next-generation sequencing (NGS) for a radish inbred line, and 76,592 scaffolds of >= 300 bp were constructed along with the bacterial artificial chromosome-end sequences. Finally, the whole draft genomic sequence of 402 Mb spanning 75.9% of the estimated genomic size and containing 61,572 predicted genes was obtained. Subsequently, 221 single nucleotide polymorphism markers and 768 PCR-RFLP markers were used together with the 746 markers produced in our previous study for the construction of a linkage map. The map was combined further with another radish linkage map constructed mainly with expressed sequence tag-simple sequence repeat markers into a high-density integrated map of 1,166 cM with 2,553 DNA markers. A total of 1,345 scaffolds were assigned to the linkage map, spanning 116.0 Mb. Bulked PCR products amplified by 2,880 primer pairs were sequenced by NGS, and SNPs in eight inbred lines were identified.
引用
收藏
页码:481 / 490
页数:10
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