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林业科学 ›› 2019, Vol. 55 ›› Issue (2): 41-49.doi: 10.11707/j.1001-7488.20190205

• 论文与研究报告 • 上一篇    下一篇

极小种群濒危植物盐桦叶绿体基因组特征分析

于涛1, 张宇阳1, 高健2, 柯蕾1, 马文宝3, 李俊清1   

  1. 1. 北京林业大学 森林资源生态系统过程北京市重点实验室 北京 100083;
    2. 包头师范学院资源与环境学院 包头 014030;
    3. 四川省林业科学研究院 国家林业和草原局四川森林生态与资源环境重点实验室 成都 610081
  • 收稿日期:2018-03-05 修回日期:2018-06-26 出版日期:2019-02-25 发布日期:2019-03-20
  • 基金资助:
    国家重点研发计划项目(2016YFC0503106)。

Complete Chloroplast Genome Sequence of Betula halophila, a Plant Species with Extremely Small Populations

Yu Tao1, Zhang Yuyang1, Gao Jian2, Ke Lei1, Ma Wenbao3, Li Junqing1   

  1. 1. Beijing Key Laboratory for Forest Resources and Ecosystem Processes Beijing Forestry University Beijing 100083;
    2. Faculty of Resources and Environment, Baotou Teachers'College Baotou 014030;
    3. Key Laboratory of National Forestry and Grassland Administration on Sichuan Forest Ecology and Resources and Environment Sichuan Academy of Forestry Chengdu 610081
  • Received:2018-03-05 Revised:2018-06-26 Online:2019-02-25 Published:2019-03-20

摘要: [目的]为了解析极小种群植物盐桦叶绿体基因组结构,筛选SSRs分子标记和桦属叶绿体基因组高变区,采用高通量测序技术完成盐桦叶绿体基因组测序并与其近缘种进行比对分析。[方法]采集盐桦幼叶,使用TIANGEN试剂盒提取DNA并利用HiSeq Xten测序平台进行测序。以欧洲矮桦叶绿体基因组作为参考,使用MITObim v1.8和NOVOplasty软件拼接组装盐桦叶绿体基因组,并利用生物信息学手段进行特征分析。[结果]利用质量控制后的30 000 000条clean data,成功拼接完成序列全长为160 648 bp的盐桦叶绿体基因组,NCBI登录号为MG674393。其中,大单拷贝(LSC)区段长度89 553 bp,GC含量33.7%,小单拷贝(SSC)区段长19 027 bp,GC含量为29.7%,2个反向重复区(IRs)区段均为26 034 bp,GC含量42.5%。成功注释了盐桦叶绿体基因组共114个基因,其中包括79个蛋白编码基因,31个tRNA基因和4个rRNA基因。盐桦叶绿体基因组含有91个SSRs位点,其中33个SSRs均由A或T组成。SSRs主要分布于LSC区,56个SSRs位于LSC区,13个SSRs位于SSC区,而IRs区有22个SSRs。对盐桦和欧洲矮桦叶绿体全基因组进行比对分析,结果显示ndhC-trnVpetA-psbJrpl22-rps19区域的核酸变异度(π>0.2)显著高于其他区域,高变区的位置都位于LSC区,而IRs区和SSC区内2种植物变异度较小。正选择分析显示ycf1,rpoC1,rpl2ndhA 4个基因出现正选择信号。盐桦、欧洲矮桦与其他双子叶植物共14条叶绿体全基因组序列通过MP、NJ方法进行聚类分析,MP和NJ树中的11个节点中有9个支持度为100%。支持盐桦和欧洲矮桦亲缘关系最近,桦木属物种与天目铁木在同一分支。[结论]通过高通量测序和生物信息学分析,得到盐桦叶绿体基因组。比对分析表明结构、基因组成和SSRs分布都与欧洲矮桦叶绿体基因组相似,二者在3个片段区域存在较高的核酸多态性,可作为桦属植物叶绿体基因组高分辨率的分子条形码。正选择分析确定有4个基因出现正选择信号(ycf1,rpoC1,rpl2,ndhA)。本研究结果可为极小濒危植物盐桦的保护工作提供重要的遗传背景信息。

关键词: 盐桦, 叶绿体基因组, 高通量测序, 系统发育

Abstract: [Objective] Betula halophila was recorded as an endangered species in the list of plant species with extremely small populations (PSESPs).In this study,we used high-throughput sequencing technology to sequence its chloroplast (cp) genome to understand the structure of B.halophila cp genome as well as the potential simple sequence repeats (SSRs) markers.We also compared the cp genome of B.halophila with those of the phylogenetically related species to understand the hotspot region in Betulaceae.[Method] Total genomic DNA was extracted from fresh leaf samples using the Plant Genomic DNA Kit (Tiangen Biotech).The HiSeq Xten platform was used for library construction and sequencing.MITObim v1.8 and NOVOplasty were used to assemble trimmed reads with the cp genome of B.nana as the reference.[Result] Totally,30 000 000 reads were obtained after trimming.The B.halophila cp genome (Accession Number MG674393 in NCBI) was a typical circular double-stranded DNA molecule with 160 648 bp in length,and its quadripartite structure was similar to most angiosperms,which comprised of LSC region (89 553 bp,GC content 33.7%),SSC regions (18 159 bp,GC content 29.7%) and IRs regions (IRa and IRb,26 689 bp each,GC content 42.5%).Four unique rRNAs,31 tRNAs,and 79 protein-coding genes were annotated.We further detected 91 SSRs,of which 33 SSRs were composed of A or T,and 56,13,and 22 SSRs were at the LSC,SSC and IRs,respectively.The sliding window analysis showed three highly variable regions (hotspots) under a criterion of nucleotide variability >0.2:ndhC-trnV,petA-psbJ,and rpl22-rps19.All of these hotspots locate at the LSC region.In contrast,the SSC and IRs regions are relatively conservative.In addition,four genes of ycf1,rpoC1,rpl2,and ndhA were signaled with positive selection.Phylogenomic reconstruction with 13 dicotyledonous plants revealed that nine of the 11 nodes had 100% supports for grouping in both MP and NJ trees.The phylogenomic analysis indicated that B.halophila was close to B.nana and sister with Ostrya rehderiana.[Conclusion] Via the high-throughput sequencing and the bioinformatic analyses of the cp genome of B.halophila,we found the similar organization,gene contents and SSRs distribution with B.nana cp genomes.Three identified highly variable regions in LSC are applicable for DNA barcodes for species identification,plant breeding,and phylogenetic inference.Four positively selected genes deserve further investigation.It provides important genetic information for the future protection of B.halophila.

Key words: Betula halophila, chloroplast genome, high-throughput sequencing, phylogenetic analysis

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