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园艺学报 ›› 2018, Vol. 45 ›› Issue (2): 309-320.doi: 10.16420/j.issn.0513-353x.2017-0310

• 研究论文 • 上一篇    下一篇

桂花LTR类反转录转座子RT序列的克隆及分析

王庆竹1,2,李慧平2,文晓鹏2,范付华1,3,*   

  1. 1贵州大学林学院,贵阳 550025;2贵州大学贵州省农业生物工程重点实验室,贵阳 550025;3贵州大学贵州省森林资源与环境研究中心,贵阳 550025
  • 出版日期:2018-02-25 发布日期:2018-02-25
  • 基金资助:

    贵州省联合基金项目(黔科合LH字[2017]7258);贵州大学2017年度学术新苗培养及创新探索专项(黔科合平台人才[2017]5788);贵州大学研究生创新基金项目(研农2017016)

Cloning and Analysis of Reverse Transcriptase of LTR Retrotransposons in Osmanthus fragrans

WANG Qingzhu1,2,LI Huiping2,WEN Xiaopeng2,and FAN Fuhua1,3,*   

  1. 1College of ForestryGuizhou UniversityGuiyang 550025China2Guizhou Key Laboratory of Agricultural BioengineeringGuizhou UniversityGuiyang 550025China3Institute for Forestry Resources & Environment of GuizhouGuizhou UniversityGuiyang 550025China
  • Online:2018-02-25 Published:2018-02-25

摘要:

克隆获得桂花Ty1-copia和Ty3-gypsy类反转录转座子反转录酶(reverse transcriptase,RT)序列,并对其序列变化特点进行分析,以期为桂花基因组进化和多样性研究提供依据。根据Ty1-copia和Ty3-gypsy类反转录转座子RT保守区设计简并引物,以桂花叶片基因组DNA为模板,通过PCR扩增,分别得到260和430 bp左右的目标条带,经回收、克隆、测序及相关生物信息学软件进行序列分析后,获得49条Ty1-copia类反转录转座子RT序列和20条Ty3-gypsy类反转录转座子RT序列。通过核苷酸聚类,Ty1-copia类反转录转座子RT序列分为4类。这些序列长度为255 ~ 271 bp,序列相似性为32.0% ~ 96.9%。翻译成氨基酸后,有2条序列出现移码突变,16条序列出现终止密码子突变。Ty3-gypsy类反转录转座子RT序列也分为4类。序列长度为408 ~ 449 bp,相似性为54.7% ~ 98.8%。有8条序列发生移码突变,10条序列发生终止密码子突变。经反转录转座子RT氨基酸序列比对,桂花与梅花、李、枣等可能有共同的起源。桂花Ty1-copia和Ty3-gypsy类反转录转座子RT序列具有高度异质性;系统进化树分析表明,桂花与不同物种间可能存在反转录转座子的横向传递。

关键词: 桂花, 反转录转座子, Ty1-copia, Ty3-gypsy, 反转录酶, 异质性

Abstract:

To provide theoretical basis for genetic evolution and diversity of Osmanthus fragrans,reverse transcriptase(RT)sequences of Ty1-copia and Ty3-gypsy-like retrotransposon were cloned and analyzed in the genome. Using degenerate oligonucleotide primers corresponding to conserved domains of Ty1-copia and Ty3-gypsy LTR retrotransposon RT sequence,fragments of 260 bp and 430 bp were amplified by polymerase chain reaction(PCR)from genomic DNA of leaves,respectively. Then,the products were purified and sub-cloned to pMD-19-T vector. Subsequently,49 RT sequences of Ty1-copia-like retrotransposon and 20 of Ty3-gypsy-like retrotransposon were obtained through sequencing and related bioinformatics analysis. RT sequences of Ty1-copia-like retrotransposon were classified into four groups after cluster and alignment analyses of their nucleotide sequences. The length of the nucleotide sequences varied from 255 to 271 bp,and homology ranged from 32.0% to 96.9%. When RT nucleotide sequences translated into amino acids,two sequences showed frameshift mutation,and sixteen sequences presented stop codon mutation. Four groups were clustered by alignment analyses of RT nucleotide sequences of Ty3-gypsy-like retrotransposon. The length of the nucleotide sequences varied from 408 to 449 bp,and homology ranged from 54.7% to 98.8%. The deduction of amino acids revealed that 8 sequences presented frameshift mutation and 10 sequences presented stop codon mutation. Phylogenic trees were constructed based on the amino acid sequences from other species,indicating that Osmanthus fragrans had homologies with Prunus mumePrunus salicina as well as Ziziphus jujuba. The RT nucleotide sequence of Ty1-copia and Ty3-gypsy retrotransposon were highly heterogeneous. Phylogenetic analysis demonstrated that Osmanthus fragrans showed a common origin with other species,and a horizontal transmission of retrotransposons occurred among different species in the process of evolution.

Key words: Osmanthus fragrans, retrotransposon, Ty1-copia, Ty3-gypsy, reverse transcriptase, heterogeneity

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