首页 | 期刊简介 | 编委会 | 投稿指南 | 常用下载 | 联系我们 | 期刊订阅 | In English
引用本文:柳淑芳,吴仁协,朱 玲,庄志猛.小黄鱼(Larimichthys polyactis)线粒体基因组结构与特征.海洋与湖沼,2010,41(6):885-894.
【打印本页】   【HTML】   【下载PDF全文】   查看/发表评论  下载PDF阅读器  关闭
←前一篇|后一篇→ 过刊浏览    高级检索
本文已被:浏览 2533次   下载 1594 本文二维码信息
码上扫一扫!
分享到: 微信 更多
小黄鱼(Larimichthys polyactis)线粒体基因组结构与特征
柳淑芳1, 吴仁协1,2, 朱 玲1, 庄志猛1
1.山东省渔业资源与生态环境重点实验室 中国水产科学研究院黄海水产研究所;2.广东海洋大学水产学院
摘要:
采用长片段扩增策略, 获得鲈形目石首鱼科黄鱼属小黄鱼的线粒体基因组全序列。组装分析结果表明, 其长度为 16470bp, H 链碱基组成呈明显反 G 偏倚, G 含量仅为 16%。13 个蛋白质基因起始密码子均为 ATG。COI 基因的终止密码子为 AGA, ND1 和 ND3 基因为 TAG, COII、ND4 和 Cyt b 基因为不完全终止密码子 T, 其余 7 个基因都是完整的 TAA。在小黄鱼 mtDNA 中发现 2 个特殊发夹结构, 一个是轻链复制起始区(OL)的发夹环, 位于tRNA簇, 环区T含量仅为9%, 而G含量达45%, 这与哺乳动物和爪蟾该区域富含 T 有所不同。另一个假定发夹结构位于 ATP6 基因末端, 这种二级结构可能与准确转录有关。该 mtDNA 控制区长度为 799bp, 5′端含有 9 个连续 TA 串联重复和 2 个5′-ATGTA---TACAT-3′重复, 与已报道的鱼类扩展终止相关序列模式恰恰相反; 中央控制区仅识别出CSB-E 结构; 保守序列区含有 CSB-1, 2, 3, 其中 CSB-2 具有高度保守性。对小黄鱼和大黄鱼的mtDNA 比较进化研究, 根据分子钟假说, 估计二者线粒体基因组的进化分歧时间为 4.8 百万年前。
关键词:  小黄鱼, 线粒体基因组, 比较进化
DOI:10.11693/hyhz201006014014
分类号:
基金项目:国家自然科学基金项目, 40776097 号, 31061160187 号; 国家高技术研究发展计划项目, 2009AA09Z401 号; 山东省泰山学者工程专项, 2009.03—2014.02。
附件
COMPLETE SEQUENCE AND GENE ORGANIZATION OF MITOCHONDRIAL DNA OF THE SMALL YELLOW CROAKER LARIMICHTHYS POLYACTIS
LIU Shu-Fang1, WU Ren-Xie1,2, ZHU Ling1, ZHUANG Zhi-Meng1
1.Key Laboratory for Fishery Resources and Eco-environment, Shandong Province, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences;2.College of Fisheries, Guangdong Ocean University
Abstract:
Based on the conserved region in mitochondrial DNA of Perciformes, the primers were designed to determine the complete mtDNA sequence of small yellow croaker Larimichthys polyactis by long PCR technique. As sequenced, the length was 16470bp, containing 13 protein-coding genes, two rRNA genes, 22 tRNA genes and non-coding regions. The total base composition of H strand was characterized by the negative bias for G (16%). All protein-coding genes of L. polyactis mtDNA used ATG as the initiation codons. Seven protein- coding genes terminated with TAA. COI gene ended with TGA; ND1 and ND3 genes ended with TAG; and COII, ND4, Cyt b genes ended with incomplete stop codon, i.e. a single stop nucleotide T. Two putative hairpin structures were detected in this species. One was in the origin of the light strand replication (OL), which was located in a cluster of five tRNA genes (tRNA-Trp, Ala, Asn, Cys and Tyr). The other hairpin structure was identified in the end of ATP6 gene, This secondary structure might be related to the mtDNA transcription. The control region of L. polyactis was located between tRNAPro and tRNAPhe, with 799bp in length. Nine copies of TA tandem repeats and two repeats “-ATGTA---TACAT-” were found in 5′-end of control region. Only CSB-E was detected in central conserved domain. Three conserved sequence blocks CSB-1, CSB-2 and CSB-3 were found at the 3′-end of the control region. CSB-2 was the most conservative in fishes. Compared with the mtDNA of large yellow croaker L. crocea, the DNA sequence similarity of 12S and 16S rRNA genes was the highest (96%), while the amino acid sequence similarity of ND6 gene was the lowest (83%). According to the molecular clock, the divergence between small and large yellow croaker happened 4.8 million years ago by compared with their mtDNA sequences.
Key words:  Small yellow croaker Larimichthys polyactis, Mitochondrion genome, Comparative evolution
版权所有 海洋与湖沼 Oceanologia et Limnlolgia Sinica Copyright©2008 All Rights Reserved
主管单位:中国科协技术协会 主办单位:中国海洋湖沼学会
地址:青岛市海军路88号  邮编:266400  电话:0532-82898753  E-mail:ols@qdio.ac.cn
技术支持:北京勤云科技发展有限公司