Unique mammalian tRNA-derived repetitive elements in dermopterans: the t-SINE family and its retrotransposition through multiple sources

被引:28
作者
Piskurek, O
Nikaido, M
Boeadi
Baba, M
Okada, N [1 ]
机构
[1] Tokyo Inst Technol, Fac Biosci & Biotechnol, Dept Sci Biol, Yokohama, Kanagawa 227, Japan
[2] Puslitbang Biol LIPI, Museum Zoologi Bogor, Cibinong, Indonesia
[3] Kitakyushu Museum, Kitakyushu, Fukuoka, Japan
[4] Inst Nat Hist, Kitakyushu, Fukuoka, Japan
[5] Natl Inst Basic Biol, Dept Cell Biol, Okazaki, Japan
关键词
t-SINE; tRNA-derived; subfamilies; multiple source gene model; Cynocephalus variegatus; Dermoptera;
D O I
10.1093/molbev/msg187
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Short interspersed nuclear elements (SINEs) are dispersed repetitive DNA sequences that are major components of all mammalian genomes. They have been described in almost all lineages of Euarchontoglires (rodents, rabbits, primates, flying lemurs, and tree shrews), except in flying lemurs. Most SINE family members are composed of three distinct regions: a 5' tRNA-related region, a tRNA-unrelated region, and a short tandem repeat at the 3' end that is AT-rich. The newly discovered SINE family in Cynocephalus deviates from this common structure. All 30 SINE loci analyzed in this family lack a tRNA-unrelated region and are composed exclusively of tRNA-related elements. Therefore, this novel SINE structure, described for the first time in mammalian genomes, was designated as t-SINE. The t-SINE family exhibits a high copy number and is specific to flying lemurs. Three major t-SINE subfamilies could be distinguished on the basis of characteristic nucleotides, deletions, insertions, and duplications. These sequence-specific characteristics within subfamilies and sub-subfamilies reveal that they are derived copies of distinct progenitors. We present evolutionary relationships between subfamilies and compare relationships between the subfamilies and the isoleucine tRNA gene. t-SINE amplification occurred through multiple sources and is supposedly mobilized via the L1-encoded reverse transcriptase-dependent retrotranspositional mechanism in trans.
引用
收藏
页码:1659 / 1668
页数:10
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