College of Horticulture, Shenyang Agricultural University, 120 Dongling Road, Shenhe District, Shenyang, People's Republic of China.
Theor Appl Genet. 2020 Oct;133(10):2937-2948. doi: 10.1007/s00122-020-03647-4. Epub 2020 Jul 12.
Mapping and resequencing of two allelic early bolting mutants ebm5-1 and ebm5-2 revealed that the BrSDG8 gene is related to bolting in Chinese cabbage (Brassica rapa ssp. pekinensis). Bolting influences the leafy head formation and seed yield of Chinese cabbage therefore being an important agronomic trait. Herein, two allelic early bolting mutants, ebm5-1 and ebm5-2, stably inherited in Chinese cabbage were obtained from wild-type 'FT' seeds by ethyl methane sulfonate mutagenesis. Both mutants flowered significantly earlier than 'FT,' and genetic analysis revealed that the early bolting of the two mutants was controlled by one recessive nuclear gene. With BSR-seq, the mutations originating lines ebm5-1 and ebm5-2 were located to the same region in chromosome A07. Using the 1741 F individuals with the ebm5-1 phenotype as the mapping population, this region was narrowed to 56.24 kb between markers InDel18 and InDel45. A single-nucleotide polymorphism (SNP) was aligned to the BraA07g040740.3C (BrSDG8) region by whole-genome resequencing of ebm5-1 mutant and 'FT.' BrSDG8 is a homolog of Arabidopsis thaliana SDG8 encoding a histone methyltransferase affecting H3K4 trimethylation in FLOWERING LOCUS C chromatin. Comparative sequencing established that the SNP occurred on BrSDG8 17th exon in ebm5-1. Genotype analysis showed full co-segregation of the early bolting phenotype with this SNP. Cloning of allelic mutant ebm5-2 indicated that it harbors a deletion mutation on the 12th exon of BrSDG8. Quantitative real-time PCR analysis indicated that BrSDG8 expression level was observably lower in mutant ebm5-1 than in 'FT.' Overall, the present results provide strong evidence that BrSDG8 mutation leads to early bolting in Chinese cabbage, thereby providing a basis to understand the molecular mechanisms underlying this phenotype.
两个等位早花突变体 ebm5-1 和 ebm5-2 的作图和重测序表明,BrSDG8 基因与白菜( Brassica rapa ssp. pekinensis )的抽薹有关。抽薹会影响白菜的叶球形成和种子产量,因此是一个重要的农艺性状。本文中,通过乙基亚硝基脲诱变从野生型“FT”种子中获得了两个稳定遗传的白菜等位早花突变体 ebm5-1 和 ebm5-2。这两个突变体的开花时间均明显早于“FT”,遗传分析表明,这两个突变体的早花受一个隐性核基因控制。通过 BSR-seq,将突变体 ebm5-1 和 ebm5-2 的突变所在系定位到 A07 号染色体的同一区域。利用 ebm5-1 表型的 1741 F 个体作为作图群体,将该区域缩小到标记 InDel18 和 InDel45 之间的 56.24 kb。通过对 ebm5-1 突变体和“FT”的全基因组重测序,将一个单核苷酸多态性(SNP)与 BraA07g040740.3C(BrSDG8)区域进行比对。BrSDG8 是拟南芥 SDG8 的同源物,编码一种组蛋白甲基转移酶,影响 FLOWERING LOCUS C 染色质中 H3K4 的三甲基化。比较测序确定 ebm5-1 中的 SNP 发生在 BrSDG8 的第 17 个外显子上。基因型分析表明,该 SNP 与早花表型完全共分离。等位突变体 ebm5-2 的克隆表明,它在 BrSDG8 的第 12 个外显子上存在缺失突变。定量实时 PCR 分析表明,突变体 ebm5-1 中 BrSDG8 的表达水平明显低于“FT”。总体而言,本研究结果提供了强有力的证据表明 BrSDG8 突变导致白菜的早花,从而为理解该表型的分子机制提供了依据。