Department of Bioscience and Bioinformatics, Myongji University, Yongin, 17058, Korea.
Department of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Korea.
Theor Appl Genet. 2022 May;135(5):1731-1750. doi: 10.1007/s00122-022-04066-3. Epub 2022 Mar 6.
This study presents an improved genome of Raphanus sativus cv. WK10039 uncovering centromeres and differentially methylated regions of radish chromosomes. Comprehensive genome comparison of radish and diploid Brassica species of U's triangle reveals that R. sativus arose from the Brassica B genome lineage and is a sibling species of B. nigra. Radish (Raphanus sativus L.) is a key root vegetable crop closely related to the Brassica crop species of the family Brassicaceae. We reported a draft genome of R. sativus cv. WK10039 (Rs1.0), which had 54.6 Mb gaps. To study the radish genome and explore previously unknown regions, we generated an improved genome assembly (Rs2.0) by long-read sequencing and high-resolution genome-wide mapping of chromatin interactions. Rs2.0 was 434.9 Mb in size with 0.27 Mb gaps, and the N50 scaffold length was 37.3 Mb (40-fold larger assembly compared to Rs1.0). Approximately 38% of Rs2.0 was comprised of repetitive sequences, and 52,768 protein-coding genes and 4845 non-protein-coding genes were predicted and annotated. The improved contiguity and coverage of Rs2.0, along with the detection of highly methylated regions, enabled localization of centromeres where R. sativus-specific centromere-associated repeats, full-length OTA and CRM LTR-Gypsy retrotransposons, hAT-Ac, CMC-EnSpm and Helitron DNA transposons, and sequences highly homologous to B. nigra centromere-specific CENH3-associated CL sequences were enriched. Whole-genome bisulfite sequencing combined with mRNA sequencing identified differential epigenetic marks in the radish genome related to tissue development. Synteny comparison and genomic distance analysis of radish and three diploid Brassica species of U's triangle suggested that the radish genome arose from the Brassica B genome lineage through unique rearrangement of the triplicated ancestral Brassica genome after splitting of the Brassica A/C and B genomes.
本研究提供了一个改良的萝卜基因组,揭示了萝卜染色体的着丝粒和差异甲基化区域。对 U 三角的萝卜和二倍体芸薹属物种的综合基因组比较表明,萝卜起源于芸薹属 B 基因组谱系,是黑芥的姊妹种。萝卜(Raphanus sativus L.)是一种重要的根茎类蔬菜作物,与芸薹属作物密切相关。我们报道了萝卜 cv. WK10039(Rs1.0)的基因组草图,该基因组有 54.6 Mb 的缺口。为了研究萝卜基因组并探索未知区域,我们通过长读测序和高分辨率全基因组染色质相互作用作图生成了一个改良的基因组组装(Rs2.0)。Rs2.0 的大小为 434.9 Mb,有 0.27 Mb 的缺口,N50 支架长度为 37.3 Mb(与 Rs1.0 相比,组装规模扩大了 40 倍)。Rs2.0 约有 38%的序列为重复序列,预测和注释了 52768 个蛋白质编码基因和 4845 个非蛋白质编码基因。Rs2.0 的连续性和覆盖度得到了改善,同时检测到高度甲基化区域,从而定位了萝卜特有的着丝粒相关重复序列、全长 OTA 和 CRM LTR-Gypsy 反转录转座子、hAT-Ac、CMC-EnSpm 和 Helitron DNA 转座子以及与黑芥着丝粒特异性 CENH3 相关 CL 序列高度同源的区域。全基因组亚硫酸氢盐测序结合 mRNA 测序鉴定了与组织发育相关的萝卜基因组中的差异表观遗传标记。萝卜与 U 三角的三个二倍体芸薹属物种的共线性比较和基因组距离分析表明,萝卜基因组起源于芸薹属 B 基因组谱系,是在芸薹属 A/C 和 B 基因组分裂后,通过三倍体祖先芸薹属基因组的独特重排形成的。