Li Guangguang, Jiang Ding, Wang Juntao, Liao Yi, Zhang Ting, Zhang Hua, Dai Xiuchun, Ren Hailong, Chen Changming, Zheng Yansong
Guangzhou Academy of Agricultural Sciences, Guangzhou 510335, China.
College of Horticulture, South China Agricultural University, Guangzhou 510642, China.
Plants (Basel). 2023 Jun 29;12(13):2498. doi: 10.3390/plants12132498.
Chinese flowering cabbage ( var. ) is a popular and widely cultivated leaf vegetable crop in Asia. Here, we performed a high quality assembly of the 384 Mb genome of 10 chromosomes of a typical cultivar of Chinese flowering cabbage with an integrated approach using PacBio, Illumina, and Hi-C technology. We modeled 47,598 protein-coding genes in this analysis and annotated 52% (205.9/384) of its genome as repetitive sequences including 17% in DNA transposons and 22% in long terminal retrotransposons (LTRs). Phylogenetic analysis reveals the genome of the Chinese flowering cabbage has a closer evolutionary relationship with the AA diploid progenitor of the allotetraploid species, . Comparative genomic analysis of Brassica species with different subgenome types (A, B and C) reveals that the pericentromeric regions on chromosome 5 and 6 of the AA genome have been significantly expanded compared to the orthologous genomic regions in the BB and CC genomes, largely driven by LTR-retrotransposon amplification. Furthermore, we identified a large number of structural variations (SVs) within the lines that could impact coding genes, suggesting the functional significance of SVs on Brassica genome evolution. Overall, our high-quality genome assembly of the Chinese flowering cabbage provides a valuable genetic resource for deciphering the genome evolution of Brassica species and it can potentially serve as the reference genome guiding the molecular breeding practice of crops.
菜心(变种)是亚洲一种广受欢迎且广泛种植的叶菜类作物。在此,我们采用PacBio、Illumina和Hi-C技术相结合的方法,对一个典型菜心品种的10条染色体、384 Mb的基因组进行了高质量组装。在该分析中,我们构建了47,598个蛋白质编码基因的模型,并将其基因组的52%(205.9/384)注释为重复序列,其中包括17%的DNA转座子和22%的长末端反转录转座子(LTR)。系统发育分析表明,菜心的基因组与异源四倍体物种的AA二倍体祖先在进化关系上更为密切。对具有不同亚基因组类型(A、B和C)的芸苔属物种进行比较基因组分析发现,与BB和CC基因组中的直系同源基因组区域相比,AA基因组第5和第6号染色体的着丝粒周围区域显著扩展,这主要是由LTR反转录转座子扩增驱动的。此外,我们在品系中鉴定出大量可能影响编码基因的结构变异(SV),表明SV对芸苔属基因组进化具有功能意义。总体而言,我们对菜心的高质量基因组组装为解读芸苔属物种的基因组进化提供了宝贵的遗传资源,并且它有可能作为参考基因组指导菜心作物的分子育种实践。