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Tiggers and DNA transposon fossils in the human genome.
Abstract
We report several classes of human interspersed repeats that resemble fossils of DNA transposons, elements that move by excision and reintegration in the genome, whereas previously characterized mammalian repeats all appear to have accumulated by retrotransposition, which involves an RNA intermediate. The human genome contains at least 14 families and > 100,000 degenerate copies of short (180-1200 bp) elements that have 14- to 25-bp terminal inverted repeats and are flanked by either 8 bp or TA target site duplications. We describe two ancient 2.5-kb elements with coding capacity, Tigger1 and -2, that closely resemble pogo, a DNA transposon in Drosophila, and probably were responsible for the distribution of some of the short elements. The deduced pogo and Tigger proteins are related to products of five DNA transposons found in fungi and nematodes, and more distantly, to the Tc1 and mariner transposases. They also are very similar to the major mammalian centromere protein CENP-B, suggesting that this may have a transposase origin. We further identified relatively low-copy-number mariner elements in both human and sheep DNA. These belong to two subfamilies previously identified in insect genomes, suggesting lateral transfer between diverse species.
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“Made1 elements are short miniature inverted-repeat transposable elements (MITEs), which consist of two 37 base pair (bp) terminal inverted repeats that flank 6 bp of internal sequence.”
From A Family of Human MicroRNA Genes from Miniature Inverted-Repeat Transposable Elements (2007) · cites this paper as [40]
In the citing paper
“Made1 elements were independently characterized by several groups as non-autonomous derivatives of the human mariner-like transposable element (TE) Hsmar1 [38]–[40].”
From A Family of Human MicroRNA Genes from Miniature Inverted-Repeat Transposable Elements (2007) · cites this paper as [40]
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A Family of Human MicroRNA Genes from Miniature Inverted-Repeat Transposable Elements
Piriyapongsa, J., & Jordan, I. K. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000203 · Cited by 283
DNA methylation enables transposable element-driven genome expansion
Zhou, W., Liang, G., Molloy, P. L., & Jones, P. A. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1921719117 · Cited by 181
Multiple waves of recent DNA transposon activity in the bat, Myotis lucifugus
Ray, D. A., Feschotte, C., Pagan, H. J. T., Smith, J. D., Pritham, E. J., Arensburger, P., Atkinson, P. W., & Craig, N. L. (2008) · Genome Research · doi:10.1101/gr.071886.107 · Cited by 165
Evolutionary dynamics of transposable elements in the short-tailed opossum Monodelphis domestica
Gentles, A. J., Wakefield, M. J., Kohany, O., Gu, W., Batzer, M. A., Pollock, D. D., & Jurka, J. (2007) · Genome Research · doi:10.1101/gr.6070707 · Cited by 156
Our Conflict with Transposable Elements and Its Implications for Human Disease
Burns, K. H. (2020) · Annual Review of Pathology: Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-012419-032633 · Cited by 137
Harbinger Transposons and an Ancient HARBI1 Gene Derived from a Transposase
Kapitonov, V. V., & Jurka, J. (2004) · DNA and Cell Biology · doi:10.1089/104454904323090949 · Cited by 128
SILVA, J. C., SHABALINA, S. A., HARRIS, D. G., SPOUGE, J. L., & KONDRASHOV, A. S. (2003) · Genetical Research · doi:10.1017/s0016672303006268 · Cited by 63
Metadata
- Authors
- Smit, A. F., & Riggs, A. D.
- Affiliations
- Department of Biology, Beckman Research Institute of the City of Hope, Duarte, CA 91010, USA.
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1996-02-20
- Volume
- 93
- Issue
- 4
- Pages
- 1443-1448
- ISSN
- 0027-8424
- 1091-6490
- Cited by
- 337
- References
- 0
- Language
- en
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