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Heads or tails: L1 insertion-associated 5' homopolymeric sequences

BACKGROUND: L1s are one of the most successful autonomous mobile elements in primate genomes. These elements comprise as much as 17% of primate genomes with the majority of insertions occurring via target primed reverse transcription (TPRT). Twin priming, a variant of TPRT, can result in unusual DNA...

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Autores principales: Meyer, Thomas J, Srikanta, Deepa, Conlin, Erin M, Batzer, Mark A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2837659/
https://www.ncbi.nlm.nih.gov/pubmed/20226075
http://dx.doi.org/10.1186/1759-8753-1-7
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author Meyer, Thomas J
Srikanta, Deepa
Conlin, Erin M
Batzer, Mark A
author_facet Meyer, Thomas J
Srikanta, Deepa
Conlin, Erin M
Batzer, Mark A
author_sort Meyer, Thomas J
collection PubMed
description BACKGROUND: L1s are one of the most successful autonomous mobile elements in primate genomes. These elements comprise as much as 17% of primate genomes with the majority of insertions occurring via target primed reverse transcription (TPRT). Twin priming, a variant of TPRT, can result in unusual DNA sequence architecture. These insertions appear to be inverted, truncated L1s flanked by target site duplications. RESULTS: We report on loci with sequence architecture consistent with variants of the twin priming mechanism and introduce dual priming, a mechanism that could generate similar sequence characteristics. These insertions take the form of truncated L1s with hallmarks of classical TPRT insertions but having a poly(T) simple repeat at the 5' end of the insertion. We identified loci using computational analyses of the human, chimpanzee, orangutan, rhesus macaque and marmoset genomes. Insertion site characteristics for all putative loci were experimentally verified. CONCLUSIONS: The 39 loci that passed our computational and experimental screens probably represent inversion-deletion events which resulted in a 5' inverted poly(A) tail. Based on our observations of these loci and their local sequence properties, we conclude that they most probably represent twin priming events with unusually short non-inverted portions. We postulate that dual priming could, theoretically, produce the same patterns. The resulting homopolymeric stretches associated with these insertion events may promote genomic instability and create potential target sites for future retrotransposition events.
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spelling pubmed-28376592010-03-13 Heads or tails: L1 insertion-associated 5' homopolymeric sequences Meyer, Thomas J Srikanta, Deepa Conlin, Erin M Batzer, Mark A Mob DNA Research BACKGROUND: L1s are one of the most successful autonomous mobile elements in primate genomes. These elements comprise as much as 17% of primate genomes with the majority of insertions occurring via target primed reverse transcription (TPRT). Twin priming, a variant of TPRT, can result in unusual DNA sequence architecture. These insertions appear to be inverted, truncated L1s flanked by target site duplications. RESULTS: We report on loci with sequence architecture consistent with variants of the twin priming mechanism and introduce dual priming, a mechanism that could generate similar sequence characteristics. These insertions take the form of truncated L1s with hallmarks of classical TPRT insertions but having a poly(T) simple repeat at the 5' end of the insertion. We identified loci using computational analyses of the human, chimpanzee, orangutan, rhesus macaque and marmoset genomes. Insertion site characteristics for all putative loci were experimentally verified. CONCLUSIONS: The 39 loci that passed our computational and experimental screens probably represent inversion-deletion events which resulted in a 5' inverted poly(A) tail. Based on our observations of these loci and their local sequence properties, we conclude that they most probably represent twin priming events with unusually short non-inverted portions. We postulate that dual priming could, theoretically, produce the same patterns. The resulting homopolymeric stretches associated with these insertion events may promote genomic instability and create potential target sites for future retrotransposition events. BioMed Central 2010-02-01 /pmc/articles/PMC2837659/ /pubmed/20226075 http://dx.doi.org/10.1186/1759-8753-1-7 Text en Copyright ©2010 Meyer et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Meyer, Thomas J
Srikanta, Deepa
Conlin, Erin M
Batzer, Mark A
Heads or tails: L1 insertion-associated 5' homopolymeric sequences
title Heads or tails: L1 insertion-associated 5' homopolymeric sequences
title_full Heads or tails: L1 insertion-associated 5' homopolymeric sequences
title_fullStr Heads or tails: L1 insertion-associated 5' homopolymeric sequences
title_full_unstemmed Heads or tails: L1 insertion-associated 5' homopolymeric sequences
title_short Heads or tails: L1 insertion-associated 5' homopolymeric sequences
title_sort heads or tails: l1 insertion-associated 5' homopolymeric sequences
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2837659/
https://www.ncbi.nlm.nih.gov/pubmed/20226075
http://dx.doi.org/10.1186/1759-8753-1-7
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