枇杷LTR类反转录转座子RT序列的克隆及分析  

Cloning and analysis of reverse transcriptase of LTR retrotransposons in Eriobotrya japonica

作　　者：罗昌斌 范付华 尚先文[1,3] LUO Changbin;FAN Fuhua;SHANG Xianwen(Institute for Forestry Resources&Environment of Guizhou,Guizhou University,Guiyang 550025,Guizhou,China;Key Laboratory of Forest Cultivation in Plateau Mountain of Guizhou Province,Guizhou University,Guiyang 550025,Guizhou,China;College of Forestry,Guizhou University,Guiyang 550025,Guizhou,China)

机构地区：[1]贵州大学贵州省森林资源与环境研究中心,贵阳550025 [2]贵州大学贵州省高原山地林木培育重点实验室,贵阳550025 [3]贵州大学林学院,贵阳550025

出　　处：《果树学报》2021年第4期471-484,共14页Journal of Fruit Science

基　　金：贵州省一流学科建设项目(GNYL[2017]007)。

摘　　要：【目的】揭示枇杷LTR类反转录转子座RT序列在枇杷基因组中的异质性,为枇杷转座子进化和多样性研究提供依据。【方法】以普通枇杷野生种质的叶片为材料,通过简并引物从枇杷基因组中扩增得到Ty1-copia和Ty3-gypsy类反转录转座子反转录酶序列,并对其序列变化特点进行生物信息学分析。【结果】最终获得38条Ty1-copia类RT序列和24条Ty3-gypsy类反转录转座子RT序列。其中Ty1-copia类反转录转座子RT序列的长度为257~266 bp,序列相似率为22.6%~97.6%,聚类结果显示,其核苷酸序列存在Maxium、TAR和Angela 3个支系。将核酸序列翻译为氨基酸后,有4条序列发生移码突变,12条序列发生终止密码子突变。Ty3-gypsy类反转录转座子RT序列的长度为429~438 bp,序列相似率为48.1%~99.3%,聚类结果显示,其核苷酸序列存在Tat和Reina2个支系。将核酸序列翻译为氨基酸后,有3条序列发生移码突变,7条序列发生终止密码子突变。对序列同义突变率与非同义突变率的分析结果显示,枇杷Ty1-copia和Ty3-gypsy类RT序列dN/dS均小于1。与其他植物反转录转座RT氨基酸序列进行比对,发现枇杷、梅、苹果、李可能具有共同起源。【结论】所获得的枇杷反转录转座子反转录酶氨基酸序列具有高度异质性,序列在进化过程中受到纯化选择的作用。对不同物种反转录转座RT氨基酸序列进行比对,结果表明,反转录转座子在枇杷和其他物种间可能存在横向传递。【Objective】Loquat(Eriobotrya japonica)is a fruit tree with a long history of planting,and the degree of variation is high.The activation of retrotransposon is one of the reasons for plant variation,and reverse transcriptase is the key regulatory factor of retrotransposon.Therefore,two kinds of reverse transcriptase sequences,Ty1-copia and Ty3-gypsy,were cloned from the Loquat genome using degenerate primers.The possible relationship between retrotransposon and genetic variation of loquat are explored by studying the characteristics of retrotransposons.【Methods】Using the wild loquat leaves as materials,two kinds of reverse transcriptase sequences,Ty1-copia and Ty3-gypsy,were amplified from the Loquat genome using degenerate primers.After purification,the amplified products were linked to pMDTM19-T vector and transformed into E.coli DH5αcompetent cells.After culturing at 37℃for 12-16 hours,blue and white spots were screened.Single colonies were picked out and cultured overnight in LB liquid medium containing 100 mg·L^(-1) AMP.The positive clones identified by PCR were sequenced.RT amino acid sequence was obtained by deriving and comparing with blast program on NCBI,and multiple alignment of amino acid sequence was performed by ClustalW software.The phylogenetic tree was constructed by adjacency method using MEGA7 software.DNAsp5 was used to calculate the synonymous mutation rate and non-synonymous mutation rate.【Results】After PCR amplification,Ty1-copia and Ty3-gypsy like RT sequences were obtained in the tested materials,they were about 260 bp and 430 bp and were consistent with the length of Ty1-copia and Ty3-gypsy type RT sequences reported in other plants.After the characteristic fragments were recovered and sequenced,57 Ty1-copia like RT sequences and 24 Ty3-gypsy RT sequences were obtained after removing the short sequences.The 57 Ty1-copia like RT sequences were compared with those of loquat accessed on NCBI.19 sequences with more than 95%similarity with the registered sequences were removed.

关 键 词：枇杷 反转录转座子 反转录酶 Ty1-copia Ty3-gypsy 异质性 

分 类 号：S667.3[农业科学—果树学]