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

5种鳎科鱼类核糖体ITS1序列比较
引用本文:龚理,时伟,杨敏,司李真,孔晓瑜.5种鳎科鱼类核糖体ITS1序列比较[J].水产学报,2017,41(3):321-329.
作者姓名:龚理  时伟  杨敏  司李真  孔晓瑜
作者单位:广西科学院广西红树林研究中心;中国科学院南海海洋研究所,中国科学院南海海洋研究所,中国科学院南海海洋研究所,中国科学院南海海洋研究所,中国科学院南海海洋研究所;广西科学院广西红树林研究中心
基金项目:国家自然科学(31272273);广西红树林保护与利用重点实验室开放基金资助(GKLMC-201502)通信作者:孔晓瑜,E-mail: xykong@scsio.ac.cn正文5,629字数,2个表,2个图。 *
摘    要:核糖体基因在很长一段时间内被认为严格遵循协同进化方式,但是在很多种类中都发现了明显的序列多态性,表明其是非协同进化。为了检测鳎科鱼类核糖体内转录间隔区1(ITS1)序列是否存在多态性,并探究其能否作为种类鉴定的分子标记,本研究克隆获得了5种鳎科鱼类共118条ITS1全序列。结果显示,眼斑豹鳎具有两种差异显著的片段类型,表明其在基因组中遵循非协同进化方式;而在其余4种鳎科鱼类中均没有发现序列多态性,表明其为协同进化。序列分析显示ITS1具有明显的种间长度异质性,最短的序列出现在蛾眉条鳎(412 bp),最长的为眼斑豹鳎(585 bp)。碱基分析显示ITS1序列在5种鳎科鱼类中都呈现出相同的趋势:CGAT,且GC含量为69.5%,远高于AT含量。聚类分析显示除眼斑豹鳎外,所有鳎类均单独聚为一支,种类区分度非常明显,表明ITS1序列能够作为种类鉴定的分子标记。但是眼斑豹鳎的一个克隆和东方箬鳎聚为一支,这种序列多态性对种类鉴定产生了干扰,因此用具有多态的ITS1序列作为分子标记时一定要有足够的克隆数量,避免因数据不充分而得到不正确的结论。

关 键 词:内转录间隔区  种类鉴定  分子标记  假基因  非协同进化  聚类分析
收稿时间:2016/4/14 0:00:00
修稿时间:2016/9/6 0:00:00

Comparative analysis of the first internal transcribed spacer of ribosomal DNA in five Soleidae species
GONG Li,SHI Wei,YANG Min,SI Lizhen and KONG Xiaoyu.Comparative analysis of the first internal transcribed spacer of ribosomal DNA in five Soleidae species[J].Journal of Fisheries of China,2017,41(3):321-329.
Authors:GONG Li  SHI Wei  YANG Min  SI Lizhen and KONG Xiaoyu
Institution:Guangxi Key Lab of Mangrove Conservation and Utilization, Guangxi Mangrove Research Center, Guangxi Academy of Sciences, Beihai 536000, China;Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Provincial Key Laboratory of Applied Marine Biology, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China;University of Chinese Academy of Sciences, Beijing 100049, China,Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Provincial Key Laboratory of Applied Marine Biology, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China,Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Provincial Key Laboratory of Applied Marine Biology, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China;University of Chinese Academy of Sciences, Beijing 100049, China,Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Provincial Key Laboratory of Applied Marine Biology, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China;University of Chinese Academy of Sciences, Beijing 100049, China and Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Provincial Key Laboratory of Applied Marine Biology, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China
Abstract:For a long time, the ribosomal RNA gene was thought to conform to the paradigm of strict concerted evolution pattern. In fact, an increasing number of intraindividual and intraspecies variations have been discovered, indicating a non-concerted evolution. In order to explore the polymorphism of the first internal transcribed spacer (ITS1) in the species of Soleidae of in Pleuronectiformes and whether it is applicablesuitable as a marker for species identification, a total of 118 ITS1 sequences were determined from five soles. The results showed that two distinct types were found in Pardachirus pavoninus genome, suggesting a non-concerted evolution pattern, while concerted evolution in other four solesspecies for absence of intraindividual polymorphism. Sequence analysis showdemonstrated that ITS1 had significant length heterogeneity, ranging from 412 bp in Zebrias quagga to 585 bp in P. pavoninus. The base content of sequences in all five solesspecies was in a same trend with C > G > A > T and GC % (69.5%) was far more than AT %. Except for one sequence of P. pavoninus, each of five solesspecies clustered into one clade, respectively, suggesting ITS1 sequence was suitable applicable for species identification in the present study. It is worth noting that the sequence of P. pavoninus clustered with Brachiru orientalis, suggesting that ITS1 sequence polymorphism may interfered species identification, as a result, it is essential to obtain enough clonesinvestigate the polymorphism before using ITS1 sequence as the molecular marker for species identification in order to avoid incorrect conclusions.
Keywords:internal transcribed spacer  species identification  molecular marker  pseudogene  non-concerted evolution  cluster analysis
本文献已被 CNKI 等数据库收录!
点击此处可从《水产学报》浏览原始摘要信息
点击此处可从《水产学报》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