青蒿
生物
青蒿素
核糖体DNA
人口
遗传学
内转录区
单倍型
核糖体RNA
DNA测序
基因型
基因
恶性疟原虫
系统发育学
疟疾
人口学
社会学
免疫学
作者
Xiaoxia Ding,Jieting Chen,Chen Dai,Peng Shi,Hengyu Pan,Yangyang Lin,Yikang Chen,Lu Gong,Lin-Xing Chen,Weiping Wu,Xiaohui Qiu,Jiang Xu,Zhixing Huang,Baosheng Liao
出处
期刊:Phytomedicine
[Elsevier]
日期:2023-07-01
卷期号:116: 154882-154882
标识
DOI:10.1016/j.phymed.2023.154882
摘要
Artemisia annua, a well-known traditional Chinese medicine, is the main source for production of artemisinin, an anti-malaria drug. A. annua is distributed globally, with great diversity of morphological characteristics and artemisinin contents. Diverse traits among A. annua populations impeded the stable production of artemisinin, which needs an efficient tool to identify strains and assess population genetic homogeneity.In this study, ribosomal DNA (rDNA), were characterized for A. annua for strains identification and population genetic homogeneity assessment.The ribosomal RNA (rRNA) genes were identified using cmscan and assembled using rDNA unit of LQ-9 as a reference. rDNA among Asteraceae species were compared performing with 45S rDNA. The rDNA copy number was calculated based on sequencing depth. The polymorphisms of rDNA sequences were identified with bam-readcount, and confirmed by Sanger sequencing and restriction enzyme experiment. The ITS2 amplicon sequencing was used to verify the stability of ITS2 haplotype analysis.Different from other Asteraceae species, 45S and 5S linked-type rDNA was only found in Artemisia genus. Rich polymorphisms of copy number and sequence of rDNA were identified in A. annua population. The haplotype composition of internal transcribed spacer 2 (ITS2) region which had moderate sequence polymorphism and relative short size was significantly different among A. annua strains. A population discrimination method was developed based on ITS2 haplotype analysis with high-throughput sequencing.This study provides comprehensive characteristics of rDNA and suggests that ITS2 haplotype analysis is ideal tool for A. annua strain identification and population genetic homogeneity assessment.
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