A novel method for identifying polymorphic transposable elements via scanning of high-throughput short reads

被引:10
|
作者
Kang, Houxiang [1 ]
Zhu, Dan [1 ,2 ]
Lin, Runmao [3 ]
Opiyo, Stephen Obol [4 ]
Jiang, Ning [5 ]
Shiu, Shin-Han [6 ]
Wang, Guo-Liang [1 ,7 ]
机构
[1] Chinese Acad Agr Sci, Inst Plant Protect, State Key Lab Biol Plant Dis & Insect Pest, Beijing 100193, Peoples R China
[2] Hunan Agr Univ, Dept Agron, Changsha 410128, Hunan, Peoples R China
[3] Chinese Acad Agr Sci, Inst Vegetables & flowers, Dept Plant Pathol, Beijing 100081, Peoples R China
[4] Ohio Agr Res & Dev Ctr, Mol & Cellular Imaging Ctr Columbus, Columbus, OH 43210 USA
[5] Michigan State Univ, Dept Hort, 1066 Bogue St, E Lansing, MI 48823 USA
[6] Michigan State Univ, Dept Plant Biol, E Lansing, MI 48823 USA
[7] Ohio State Univ, Dept Plant Pathol, Columbus, OH 43210 USA
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
polymorphic transposon; high-throughput sequencing; rice blast fungus; maize; DE-NOVO IDENTIFICATION; MOLECULAR ANALYSIS; GENOME SEQUENCE; DRAFT SEQUENCE; INSERTION; BLAST; TRANSPOSITION; ALIGNMENT; TRANSCRIPTION; DIVERSITY;
D O I
10.1093/dnares/dsw011
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Identification of polymorphic transposable elements (TEs) is important because TE polymorphism creates genetic diversity and influences the function of genes in the host genome. However, de novo scanning of polymorphic TEs remains a challenge. Here, we report a novel computational method, called PTEMD (polymorphic TEs and their movement detection), for de novo discovery of genome-wide polymorphic TEs. PTEMD searches highly identical sequences using reads supported breakpoint evidences. Using PTEMD, we identified 14 polymorphic TE families (905 sequences) in rice blast fungus Magnaporthe oryzae, and 68 (10,618 sequences) in maize. We validated one polymorphic TE family experimentally, MoTE-1; all MoTE-1 family members are located in different genomic loci in the three tested isolates. We found that 57.1% (8 of 14) of the PTEMD-detected polymorphic TE families in M. oryzae are active. Furthermore, our data indicate that there are more polymorphic DNA transposons in maize than their counterparts of retrotransposons despite the fact that retrotransposons occupy largest fraction of genomic mass. We demonstrated that PTEMD is an effective tool for identifying polymorphic TEs in M. oryzae and maize genomes. PTEMD and the genome-wide polymorphic TEs in M. oryzae and maize are publically available at http://www.kanglab.cn/blast/PTEMD_V1.02.htm.
引用
收藏
页码:241 / 251
页数:11
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