Hu Jian-Peng, Jiang Lu, Xu Rui, Wu Jun-Xian, Guan Feng-Ya, Yao Jin-Chen, Liu Jun-Ling, Zhang Ya-Zhong, Zha Liang-Ping
School of Pharmacy, Anhui University of Chinese Medicine Hefei 230012, China.
Anhui Institute for Food and Drug Control Hefei 230051, China.
Zhongguo Zhong Yao Za Zhi. 2023 Jan;48(1):52-59. doi: 10.19540/j.cnki.cjcmm.20221014.102.
This study investigated the choroplast genome sequence of wild Atractylodes lancea from Yuexi in Anhui province by high-throughput sequencing, followed by characterization of the genome structure, which laid a foundation for the species identification, analysis of genetic diversity, and resource conservation of A. lancea. To be specific, the total genomic DNA was extracted from the leaves of A. lancea with the improved CTAB method. The chloroplast genome of A. lancea was sequenced by the high-throughput sequencing technology, followed by assembling by metaSPAdes and annotation by CPGAVAS2. Bioiformatics methods were employed for the analysis of simple sequence repeats(SSRs), inverted repeat(IR) border, codon bias, and phylogeny. The results showed that the whole chloroplast genome of A. lancea was 153 178 bp, with an 84 226 bp large single copy(LSC) and a 18 658 bp small single copy(SSC) separated by a pair of IRs(25 147 bp). The genome had the GC content of 37.7% and 124 genes: 87 protein-coding genes, 8 rRNA genes, and 29 tRNA genes. It had 26 287 codons and encoded 20 amino acids. Phylogenetic analysis showed that Atractylodes species clustered into one clade and that A. lancea had close genetic relationship with A. koreana. This study established a method for sequencing the chloroplast genome of A. lancea and enriched the genetic resources of Compositae. The findings are expected to lay a foundation for species identification, analysis of genetic diversity, and resource conservation of A. lancea.
本研究采用高通量测序技术对安徽岳西野生苍术的叶绿体基因组序列进行了测定,随后对基因组结构进行了表征,为苍术的物种鉴定、遗传多样性分析和资源保护奠定了基础。具体而言,采用改良CTAB法从苍术叶片中提取总基因组DNA。利用高通量测序技术对苍术叶绿体基因组进行测序,随后通过metaSPAdes进行组装,并通过CPGAVAS2进行注释。运用生物信息学方法对简单序列重复(SSR)、反向重复(IR)边界、密码子偏好性和系统发育进行分析。结果表明,苍术叶绿体全基因组长度为153178 bp,其中大单拷贝区(LSC)为84226 bp,小单拷贝区(SSC)为18658 bp,由一对反向重复序列(IR)(25147 bp)隔开。基因组的GC含量为37.7%,共有124个基因:87个蛋白质编码基因、8个rRNA基因和29个tRNA基因。它有26287个密码子,编码20种氨基酸。系统发育分析表明,苍术属物种聚为一个分支,苍术与朝鲜苍术亲缘关系较近。本研究建立了苍术叶绿体基因组测序方法,丰富了菊科的遗传资源。这些研究结果有望为苍术的物种鉴定、遗传多样性分析和资源保护奠定基础。