Alu retrotransposition-mediated deletion
- PMID: 15843013
- DOI: 10.1016/j.jmb.2005.02.043
Alu retrotransposition-mediated deletion
Abstract
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.
Similar articles
-
Recently integrated Alu elements and human genomic diversity.Mol Biol Evol. 2003 Aug;20(8):1349-61. doi: 10.1093/molbev/msg150. Epub 2003 May 30. Mol Biol Evol. 2003. PMID: 12777511
-
Non-traditional Alu evolution and primate genomic diversity.J Mol Biol. 2002 Mar 8;316(5):1033-40. doi: 10.1006/jmbi.2001.5380. J Mol Biol. 2002. PMID: 11884141
-
Alu repeats and human genomic diversity.Nat Rev Genet. 2002 May;3(5):370-9. doi: 10.1038/nrg798. Nat Rev Genet. 2002. PMID: 11988762 Review.
-
Alu repeats and human disease.Mol Genet Metab. 1999 Jul;67(3):183-93. doi: 10.1006/mgme.1999.2864. Mol Genet Metab. 1999. PMID: 10381326 Review.
-
Attempts to detect retrotransposition and de novo deletion of Alus and other dispersed repeats at specific loci in the human genome.Eur J Hum Genet. 2001 Feb;9(2):143-6. doi: 10.1038/sj.ejhg.5200590. Eur J Hum Genet. 2001. PMID: 11313748
Cited by
-
Novel Gross Deletion Mutations in NTRK1 Gene Associated With Congenital Insensitivity to Pain With Anhidrosis.Front Pediatr. 2021 Mar 4;9:638190. doi: 10.3389/fped.2021.638190. eCollection 2021. Front Pediatr. 2021. PMID: 33748046 Free PMC article.
-
High Levels of Sequence Diversity in the 5' UTRs of Human-Specific L1 Elements.Comp Funct Genomics. 2012;2012:129416. doi: 10.1155/2012/129416. Epub 2012 Feb 7. Comp Funct Genomics. 2012. PMID: 22400009 Free PMC article.
-
Human genomic deletions mediated by recombination between Alu elements.Am J Hum Genet. 2006 Jul;79(1):41-53. doi: 10.1086/504600. Epub 2006 May 3. Am J Hum Genet. 2006. PMID: 16773564 Free PMC article.
-
Characterization of pre-insertion loci of de novo L1 insertions.Gene. 2007 Apr 1;390(1-2):190-8. doi: 10.1016/j.gene.2006.08.024. Epub 2006 Sep 12. Gene. 2007. PMID: 17067767 Free PMC article.
-
The Structural, Functional and Evolutionary Impact of Transposable Elements in Eukaryotes.Genes (Basel). 2021 Jun 15;12(6):918. doi: 10.3390/genes12060918. Genes (Basel). 2021. PMID: 34203645 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials