基于COⅠ基因的中国及邻近海域部分笛鲷属鱼类DNA条形码研究
详细信息    查看全文 | 推荐本文 |
  • 英文篇名:DNA barcoding of some Lutjanus species in China and its adjacent sea areas based on COⅠ gene
  • 作者:唐楚林 ; 肖林 ; 章群 ; 周琪 ; 徐示 ; 王业磷
  • 英文作者:TANG Chu-lin;XIAO Lin;ZHANG Qun;ZHOU Qi;XU Shi;WANG Ye-lin;Deparment of Ecology,Jinan University;
  • 关键词:COⅠ基因 ; 笛鲷属 ; DNA条形码
  • 英文关键词:COⅠ gene;;Lutjanus;;DNA barcoding
  • 中文刊名:HTYY
  • 英文刊名:Marine Fisheries
  • 机构:暨南大学生态系;
  • 出版日期:2019-03-15
  • 出版单位:海洋渔业
  • 年:2019
  • 期:v.41
  • 基金:国家自然科学基金项目(41071034);; 广东省水利科技创新项目(2016-08)
  • 语种:中文;
  • 页:HTYY201902001
  • 页数:9
  • CN:02
  • ISSN:31-1341/S
  • 分类号:4-12
摘要
笛鲷属(Lutjanus)鱼类经济价值高,物种数量多,但外部形态保守,传统分类鉴定困难。为了解中国笛鲷属鱼类的物种多样性状况,测定了中国沿海19个地点11种笛鲷73个样本线粒体COⅠ基因5'端序列,并与从GenBank下载中国及邻近海域69条同源序列进行DNA条形码分析。研究表明,勒氏笛鲷(L. russelli)、金焰笛鲷(L. fulviflamma)、奥氏笛鲷(L. ophuysenii)、约氏笛鲷(L. johni)、蓝点笛鲷(L. rivulatus)、五线笛鲷(L. quinquelineatus)、千年笛鲷(L. sebae)、紫红笛鲷(L. argentimaculatus)、白斑笛鲷(L. bohar)、马拉巴笛鲷(L. malabaricus)、黄笛鲷(L. lutjanus)、印度笛鲷(L. indicus)、画眉笛鲷(L. vitta)、星点笛鲷(L. stellatus)、四带笛鲷(L. kasmira)、驼背笛鲷(L. gibbus)、焦黄笛鲷(L. fulvus)、红鳍笛鲷(L. erythopterus)等18种笛鲷142条COⅠ序列组成18个自展数据支持率(bootstrap)为99%~100%的单系分支,分支间平均遗传距离14.4%(2.9%~21.8%)约为分支内平均遗传距离0.17%(0~0.6%)的85倍,其中10种笛鲷独立成支,支持其物种有效性。勒氏笛鲷分成2小支,小支间平均遗传距离(2.9%)是小支内平均遗传距离(0.5%)的5.8倍,未满足"10×法则",其准确的物种分类地位尚待明确。印度笛鲷与勒氏笛鲷、画眉笛鲷与奥氏笛鲷出现混杂,推测从GenBank下载的印度笛鲷序列KF830898和KF830905可能来自勒氏笛鲷;画眉笛鲷序列KU943888可能来自奥氏笛鲷。中国近海星点笛鲷和蓝点笛鲷混杂且种间遗传距离仅为2.1%,接近一般种内遗传距离2%;红鳍笛鲷和马拉巴笛鲷遗传距离种间(0.3%)与种内(0.2%~0.3%)相当,且形态相似,推测是同一物种,也不排除它们存在种间杂交和为近期分化物种的可能。
        Lutjanus is of highly economical importantance,but the wild resources have declined significantly in recent years. Although species identification is the premise of germplasm conservation,with conservative external morphological characters and rich species,the traditional morphological classification of the genus is difficult. To determine species status of some Lutjanus species in China,the 5' mitochondrial COⅠ gene sequences of 73 samples of 11 Lutjanus species from 19 locations in the coastal waters of China were sequenced,and 69 homologous sequences originated from China and adjacent waters were downloaded from GenBank,the combined analyses revealed that a total of 142 COⅠ sequences of 18 snappers(L. russelli,L.fulviflamma,L. ophuysenii,L. johni,L. rivulatus,L. quinquelineatus,L. sebae,L. argentimaculatus,L. bohar,L. malabaricus,L. lutjanus,L. indicus,L. vitta,L. stellatus,L. kasmira,L. gibbus,L. quinquelineatus,L.erythopterus) were composed of 18 distinct clades with 99% ~ 100% bootstrap support,and the average genetic distance among clades [14.4%(2.9% ~ 21.8%)] was about 85 times those within clades [0.17%(0 ~ 0.6%)]. Of which,sequences of 10 species were monophyletic,supporting their species status. L.russelli was further divided into 2 subclades,and the average genetic distance between subclades(2.9%) was 5.8 times those(0.5%) within subclades,which did not conform to the "10 × "rule,suggesting that their accurate species status remained to be determined. L. indicus and L. russelli,L. vitta and L. ophuysenii were intertwined respectively, it is deduced that GenBank downloaded L. indicus sequences KF830898 and KF830905 might be L. russelli,and L. vitta sequence KU943888 might be L. ophuysenii. L. stellatus and L.rivulatus were mixed in the same clade and the genetic distance between species was only 2.1%,which was close to the general genetic distance within species(2%). L. erythopterus and L. malabaricus were clustered in the same clade,the genetic distance between species(0.3%) was equivalent to the intraspecific genetic distance(0.2% ~ 0.3%),and the morphologyical characters were similar,thus they might be the same species,and the potential of interspecific hybridization and initial speciation should not be excluded.
引文
[1]王中铎,郭昱嵩,李路,等.笛鲷属鱼类DNA分子条码、系统进化和成种机制[J].中国科学:生命科学,2010(6):516-521.WANG Z D,GUO Y S,LI L,et al.Molecular barcode,phylogenetic and genetic mechanism of DNA of Lutjanus[J].Science China:Life Science,2010(6):516-521.
    [2]兰竹虹,陈桂珠.南中国海地区珊瑚礁资源的破坏现状及保护对策[J].生态环境学报,2006,15(2):430-434.LAN Z H,CHEN G Z.Destruction and conservation countermeasures of coral reef in South China Sea[J].Ecology and Environmental Sciences,2006,15(2):430-434.
    [3]陈作志,徐姗楠,邱永松.北部湾渔业资源及生态系统演化的回顾性分析[C]//中国水产学会学术年会论文集.2017.CHEN Z Z,XU S N,QIU Y S.Retrospective evaluation of data-limited fisheries:A case from the Beibu Gulf[C]//Annual Academic Conference of China Society of Fisheries.2017.
    [4]YAAKUB S M,BELLWOOD D R,HERWERDENL,et al.Hybridization in coral reef fishes:Introgression and bi-directional gene exchange in Thalassoma(family Labridae)[J].Molecular Phylogenetics Evolution,2006,(40):84-100.
    [5]HEBERT P D,CYWINSKA A,BALL S L,et al.Biological identifications through DNA barcodes[J].Proceedings Biological Sciences,2003,270(1512):313-321.
    [6]HEBERT P D,RATNASINGHAM S,DEWAARD JR.Barcoding animal life:Cytochrome c oxidase subunit 1 divergences among closely related species[J].Proceedings of the Royal Society of London Series B:Biological Sciences,2003,270(1):96-99.
    [7]WARD R,ZEMLAK T,INNES B,et al.DNAbarcoding Australia’s fish species[J].Philosophical Transactions of the Royal Society of London,2005,360(1462):1847-1857.
    [8]MOORE W S.Inferring phylogenies from mt DNAvariation:Mitochondral-gene trees versus nucleargene tree[J].Evolution,1995,49(4):718-726.
    [9]HEBERT P D,STOECKLE M Y,ZEMLAK T S,et al.Identification of birds though DNA barcodes[J].Plos Biology,2004,2(10):312.
    [10]WELLS R J D,JR J H C,FRY B.Feeding ecology of red snapper Lutjanus campechanus in the northern Gulf of Mexico[J].Marine Ecology Progress,2008,361(01):213-225.
    [11]唐优良,章群,余帆洋,等.基于12S rRNA部分序列分析的中国8种笛鲷科鱼类系统发育初探[J].海洋科学,2011,35(2):22-26.TANG Y L,ZHANG Q,YU F Y,et al.Phylogeny of eight snappers(Lutjanidae)in Chinese coastal waters inferred from partial mt DNA 12S rRNAsequences[J].Marine Sciences,2011,35(2):22-26.
    [12]GUO Y S,WANG Z D,LIU C W,et al.Phylogenetic relationships of South China Sea snappers(Genus Lutjanus;Family Lutjanidae)based on mitochondrial DNA sequences[J].Marine Biotechnology(NY),2007,9(6):682-688.
    [13]谭围,郭昱嵩,王中铎,等.笛鲷鱼类的线粒体DNA控制区结构及其系统发育分析[J].海洋学报,2010,32(1):139-145.TAN W,GUO Y S,WANG Z D,et al.Structure of the mitochondrial DNA control region of Lutjanus species and their phylogenetic relationship[J].Acta Oceanologica Sinica,2010,32(1):139-145.
    [14]VICTOR B C,HANNER R,SHIVJI M,et al.Identification of the larval and juvenile stages of the Cubera snapper,Lutjanus cyanopterus,using DNAbarcoding[J].Zootaxa,2009,2009(2215):24-36.
    [15]乐小亮,章群,赵爽,等.一种高效快速的鱼类标本基因组DNA提取方法[J].生物技术通报,2010,20(2):202-204.YUE X L,ZHANG Q,ZHAO S,et al.A fast and efficient method for isolation of genomic DNA from fish specimens[J].Biotechnology Bulletin,2010,20(2):202-204.
    [16]陈璐,黄伯炎,薛丹,等.中国沿海鯻科鱼类DNA条形码研究及新记录种三线鯻分类地位探讨[J].海洋渔业,2017,39(2):21-130.CHEN L,HUANG B Y,XUE D,et al.DNAbarcoding of Terapontidae and taxonomic status of a new record of Terapon puta in costal waters of China[J].Marine Fisheries,2017,39(2):121-130.
    [17]TAMURA K,DUDLEY J,NEI M,et al.MEGA4:Molecular evolutionary genetics analysis(MEGA)software version 4.0[J].Molecular Biology and Evolution,2007(24):1596-1599.
    [18]PUILLANDRE N,LAMBERT A,BROUILLET S,et al.ABGD,automatic barcode gap discovery for primary species delimitation[J].Molecular Ecology,2012,21(8):1864-1877.
    [19]KUMARS.Molecular clocks:Four decades of evolution[J].Nature Reviews Genetics,2005,6(8):654.
    [20]柳淑芳,陈亮亮,戴芳群,等.基于线粒体COⅠ基因的DNA条形码在石首鱼科(Sciaenidae)鱼类系统分类中的应用[J].海洋与湖沼,2010,41(2):223-232.LIU S F,CHEN L L,DAI F Q,et al.Applicaction of DNA barcoding gene COⅠfor classifying family Sciaenidae[J].Oceanologia et Limnologia Sinica,2010,41(2):223-232(in Chinese).
    [21]宫亚运,章群,曹艳,等.基于线粒体COⅠ基因序列的DNA条形码在中国南海绯鲤属鱼类鉴定中的应用[J].海洋渔业,2016,38(2):113-119.GONG Y Y,ZHANG Q,CAO Y,et al.Application of mitochondrial cytochrome oxidase subunit Isequence in DNA barcoding Upeneus in the South China Sea[J].Marine Fisheries,2016,38(2):113-119.
NGLC 2004-2010.National Geological Library of China All Rights Reserved.
Add:29 Xueyuan Rd,Haidian District,Beijing,PRC. Mail Add: 8324 mailbox 100083
For exchange or info please contact us via email.