首页 | 本学科首页   官方微博 | 高级检索  
   检索      

木芙蓉三个品种及近缘种的叶绿体基因组比较分析
引用本文:李镇兵,任 婷,邓姣姣,陈俊佩,周颂东,曾心美,马 娇,李方文.木芙蓉三个品种及近缘种的叶绿体基因组比较分析[J].广西植物,2022,42(12):2007-2020.
作者姓名:李镇兵  任 婷  邓姣姣  陈俊佩  周颂东  曾心美  马 娇  李方文
作者单位:1. 四川大学 生命科学学院 生物资源与生态环境教育部重点实验室, 成都 610065; 2. 成都市植物园, 成都 610083
基金项目:国家自然科学基金(32170209); 成都市植物园木芙蓉组织培养和分子育种研究项目(18H0567); 国家植物标本资源库-四川大学标本馆的数字化与共享平台(00204054A9016)[Supported by National Natural Science Foundation of China(32170209); Tissue Culture and Molecular Breeding of Hibiscus mutabilis in Chengdu Botanical Garden(18H0567); National Plant Herbarium Resource Bank-Digital and Sharing Platform of the Herbarium of Sichuan University(00204054A9016)]。
摘    要:木芙蓉(Hibiscus mutabilis)栽培历史悠久,是原产中国的古老园林树种和药用植物。为了探讨木芙蓉品种及近缘种的进化特征,厘清木芙蓉品种间及其与近缘种间的亲缘关系,以及探究木芙蓉叶绿体基因组(chloroplast DNA, cpDNA)的遗传方式,该文选择了一个杂交组合中的3个木芙蓉栽培品种(‘单瓣白’‘金秋颂’‘牡丹粉’),用高通量测序平台Illumina NovaSeq对其cpDNA进行首次测序。经组装注释后得到3条完整的cpDNA序列,结合该团队已经完成的近缘种台湾芙蓉(H.taiwanensis)和来自基因库的木槿、朱槿的cpDNA,对木槿属4种及木芙蓉种下的3个品种进行了cpDNA组成和结构特征的比较分析,并完成了其系统发育树重建。结果表明:(1)‘单瓣白’‘金秋颂’‘牡丹粉’的cpDNA序列长度分别为160 880、160 879、160 920 bp,基因数目均为130个,其中蛋白编码基因85个、核糖体RNA 8个和转运RNA 37个。(2)比较分析结果显示,木芙蓉的种下3个品种及其近缘种台湾芙蓉在cpDNA上高度保守,反向重复区(IR)均为26 300 b...

关 键 词:木芙蓉  台湾芙蓉  叶绿体基因组  分子标记  系统发育树
收稿时间:2022/2/28 0:00:00

Comparative analysis of the chloroplast genomes of three cultivars of Hibiscus mutabilis and its related species
LI Zhenbing,REN ting,DENG Jiaojiao,CHEN Junpei,ZHOU Songdong,ZENG Xinmei,MA Jiao,LI Fangwen.Comparative analysis of the chloroplast genomes of three cultivars of Hibiscus mutabilis and its related species[J].Guihaia,2022,42(12):2007-2020.
Authors:LI Zhenbing  REN ting  DENG Jiaojiao  CHEN Junpei  ZHOU Songdong  ZENG Xinmei  MA Jiao  LI Fangwen
Institution:1. College of Life Sciences, Sichuan University, Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, Chengdu 610065, China; 2. Chengdu Institute of Landscape Architecture, Chengdu 610083, China
Abstract:Hibiscus mutabilis is native to China with a long cultivation history, and is an ancient garden tree species and medicinal plant. In this study, we selected three cultivars of H. mutabilis in a hybrid combination(H. mutabilis cv. Danbanbai, H. mutabilis cv. Jinqiusong, H. mutabilis cv. Mudanfen)to investigate evolutionary characteristics between the cultivars of H. mutabilis and its related species, and clarify the phylogenetic relationship between the cultivars of H. mutabilis and its related species, as well as explore the genetic model of chloroplast genome(cpDNA)of H. mutaibilis at the same time. We first sequenced the three cultivars of H. mutaibilis using Illumina NovaSeq. After assembly and annotation, three complete chloroplast genome sequences were obtained. The cpDNAs of the related species H. taiwanensis from our group, and H. syricus and H. rosa-sinensis from the gene bank. Then we carried out comparative analysis on composition and structure of cpDNAs of four species of Hibiscus and three cultivars of H. mutabilis, and completed its phylogenetic tree reconstruction. The results were as follows:(1)Total sizes of cpDNAs of H. mutabilis cv. Danbanbai, H. mutabilis cv. Jinqiusong, H. mutabilis cv. Mudanfen were 160 880, 160 879, 160 920 bp, respectively, and the total gene number was 130, including 85 protein-coding genes, eight ribosomal RNAs, and 37 transfer RNAs.(2)The comparative analyses showed that the cpDNAs of three cultivars of H. mutabilis and the related species H. taiwanensis were highly conserved, and the inverted repeat regions(IR)were all 26 300 bp; H. rosa-sinensis and H. syriacus shrank to at 25 745 and 25 598 bp, respectively.(3)The phylogenetic analysis revealed that the three cultivars were planted into a monophyletic branch, and then together with H. taiwanensis into a high support branch, indicating that H. mutabilis and H. taiwanensis had the closest relationship; Compared with H. syriacus and H. rosa-sinensis, H. mutabilis and H. taiwanensis were more closely related to H. hamabo, H. tiliaceum and H. canabinus.(4)Three cultivars of H. mutabilis could be distinguished by cpDNA sequence, the length of LSC/SSC of H. mutabilis cv. Danbanbai, H. mutabilis cv. Jinqiusong, H. mutabilis cv. Mudanfen were 89 355 bp/18 925 bp, 89 353 bp/18 926 bp, 89 400 bp/18 920 bp, respectively. And candidate molecular markers and DNA barcodes had been developed from repeat sequence and nucleotide diversity analyses, which could be used as a tool for cultivars identification.(5)The cpDNAs of H. mutabilis cv. Danbanbai and H. mutabilis cv. Jinqiusong showed a minimum difference and had the closest phylogenetic relationship. According to the relationship between their female and offspring, the maternal genetic characteristics of the cpDNAs of Hibiscus were proved. This study will help us to understand the evolutionary characteristics and phylogenetic relationship of cpDNAs of three cultivars of H. mutabilis and H. taiwanensis, and provide basic data on cpDNA for accurate identification of the cultivars of H. mutabilis and breeding of excellent cultivars.
Keywords:Hibiscus mutabilis  Hibiscus taiwanensis  chloroplast genome(cpDNA)  molecular marker  phylogenetic tree
点击此处可从《广西植物》浏览原始摘要信息
点击此处可从《广西植物》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号