Alu retrotransposition-mediated deletion

被引:88
作者
Callinan, PA
Wang, JX
Herke, SW
Garber, RK
Liang, P
Batzer, MA
机构
[1] Louisiana State Univ, Ctr Biomol Multiscale Syst, Biol Computat & Visualizat Ctr, Dept Sci Biol, Baton Rouge, LA 70803 USA
[2] Roswell Pk Canc Inst, Dept Canc Genet, Buffalo, NY 14263 USA
关键词
short interspersed elements; target primed reverse transcription;
D O I
10.1016/j.jmb.2005.02.043
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
Alu repeats contribute to genomic instability in primates via insertional and recombinational mutagenesis. Here, we report an analysis of Alu element-induced genomic instability through a novel mechanism termed retrotransposition-mediated deletion, and assess its impact on the integrity of primate genomes. For human and chimpanzee genomes, we find evidence of 33 retrotransposition-mediated deletion events that have eliminated approximately 9000 nucleotides of genomic DNA. Our data suggest that, during the course of primate evolution, Alu retrotransposition may have contributed to over 3000 deletion events, eliminating approximately 900 kb of DNA in the process. Potential mechanisms for the creation of Alu retrotransposition-mediated deletions include L1 endonuclease-dependent retrotransposition, L1 endonuclease-independent retrotransposition, internal priming on DNA breaks, and promiscuous target primed reverse transcription. A comprehensive analysis of the collateral effects by Alu mobilization on all primate genomes will require sequenced genomes from representatives of the entire order. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:791 / 800
页数:10
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