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Identification of retrotransposon families and analysis of their transcriptional activation in wheat 被引量:1

Identification of retrotransposon families and analysis of their transcriptional activation in wheat
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摘要 Variations in the reverse transcriptase (RT) domain were analyzed to clarify retrotransposon family structure and their evolution in wheat genome. RT-PCR was conducted by using primers based on the conserved RT pep- tide motifs of plant retrotransposons to amplify the RT do- main of retrotransposons in the seedlings of wheat line Pm97034 treated with powdery mildew fungus. High level of heterogeneity was detected in 51 (RT1-51) clones randomly selected and the identity of nucleotide sequence among them ranged from 75.4% to 97.9%. These sequences, in combina- tion with previously identified seven representatives from wheat retrotransposon families (families 1―7), were used to construct a composite phylogenetic tree. Three new families, designated family 8 to family 10, were identified. Famliy 8 formed before divergence of the Pooideae subfamily and was regarged as an ancient retrotransposon family. Some mem- bers of family 4 and family 7 had transcriptional activativity, and were present with multiple copies in wheat and its re- lated species. Variations in the reverse transcriptase (RT) domain were analyzed to clarifyretrotransposon family structure and their evolution in wheat genome. RT-PCR was conducted by usingprimers based on the conserved RT pep-tide motifs of plant retrotransposons to amplify the RT domainof retrotransposons in the seedlings of wheat line Pm97034 treated with powdery mildew fungus. Highlevel of heterogeneity was detected in 51 (RT1-51) clones randomly selected and the identity ofnucleotide sequence among them ranged from 75.4 percent to 97.9 percent. These sequences, incombination with previously identified seven representatives from wheat retrotransposon families(families 1-7), were used to construct a composite phylogenetic tree. Three new families, designatedfamily 8 to family 10, were identified. Famliy 8 formed before divergence of the Pooideae subfamilyand was regarged as an ancient retrotransposon family. Some members of family 4 and family 7 hadtranscriptional activativity, and were present with multiple copies in wheat and its relatedspecies.
出处 《Chinese Science Bulletin》 SCIE EI CAS 2005年第7期630-635,共6页
基金 supported by the National Natural Science Foundation of China(Grant No.30170575).
关键词 小麦 活化作用 DNA 核酸 转换方式 植物 无性繁殖技术 Triticeae wheat retrotranspons reversetranscriptase domain evolution
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  • 1B. M. Gribbon,S. R. Pearce,R. Kalendar,A. H. Schulman,L. Paulin,P. Jack,A. Kumar,A. J. Flavell.Phylogeny and transpositional activity of Ty1-copia group retrotransposons in cereal genomes[J].MGG - Molecular and General Genetics.1999(6)
  • 2Shiping Wang,Qifa Zhang,P.J. Maughan,M.A. Maroof.Copia-like retrotransposons in rice: sequence heterogeneity, species distribution and chromosomal locations[J].Plant Molecular Biology.1997(6)
  • 3Hirohiko Hirochika,Atsushi Fukuchi,Fumio Kikuchi.Retrotransposon families in rice[J].MGG Molecular & General Genetics (-).1992(1-2)
  • 4Motoo Kimura.A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences[J].Journal of Molecular Evolution.1980(2)

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  • 1SHEN Sile1,3, WANG Zhenwei3, SHAN Xiaohui2, WANG Hua3, LI Ling3, LIN Xuyun2, LONG Likun2, WENG Kenan4, LIU Bao2 & ZOU Guangtian1 1. National Laboratory of Superhard Materials, Jilin University, Changchun 130012, China,2. Institute of Genetics and Cytology, Northeast Normal University, Changchun 130024, China,3. College of Life Science, Jilin University, Changchun 130012, China,4. Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China.Alterations in DNA methylation and genome structure in two rice mutant lines induced by high pressure[J].Science China(Life Sciences),2006,49(2):97-104. 被引量:6

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