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Science 5 March 1999: Vol. 283. no. 5407, pp. 1530 - 1534 DOI: 10.1126/science.283.5407.1530
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Reports
Exon Shuffling by L1 Retrotransposition
John V. Moran,
*
Ralph J. DeBerardinis,
Haig H. Kazazian Jr.
Long interspersed nuclear elements (LINE-1s or L1s) are the most
abundant retrotransposons in the human genome, and they serve as major
sources of reverse transcriptase activity. Engineered L1s
retrotranspose at high frequency in cultured human cells. Here it is
shown that L1s insert into transcribed genes and retrotranspose sequences derived from their 3' flanks to new genomic locations. Thus,
retrotransposition-competent L1s provide a vehicle to mobilize non-L1
sequences, such as exons or promoters, into existing genes and may
represent a general mechanism for the evolution of new genes.
Department of Genetics, University of Pennsylvania School of
Medicine, Philadelphia, PA, 19104-6145 USA.
*
Present address, Departments of Human Genetics and Internal
Medicine, University of Michigan Medical School, Ann Arbor, MI, 48109-0650 USA.
To whom correspondence should be addressed. E-mail:
moranj{at}umich.edu or kazazian{at}mail.med.upenn.edu
Read the Full Text
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PNAS
96, 12621-12625
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- Comprehensive Genome Sequence Analysis of a Breast Cancer Amplicon.
- C. Collins, S. Volik, D. Kowbel, D. Ginzinger, B. Ylstra, T. Cloutier, T. Hawkins, P. Predki, C. Martin, M. Wernick, et al. (2001)
Genome Res.
11, 1034-1042
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- A Novel Active L1 Retrotransposon Subfamily in the Mouse.
- J. L. Goodier, E. M. Ostertag, K. Du, and H. H. Kazazian Jr. (2001)
Genome Res.
11, 1677-1685
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- The Gag-like Protein of the Yeast Ty1 Retrotransposon Contains a Nucleic Acid Chaperone Domain Analogous to Retroviral Nucleocapsid Proteins.
- G. Cristofari, D. Ficheux, and J.-L. Darlix (2000)
J. Biol. Chem.
275, 19210-19217
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- Hox cluster genomics in the horn shark, Heterodontus francisci.
- C.-B. Kim, C. Amemiya, W. Bailey, K. Kawasaki, J. Mezey, W. Miller, S. Minoshima, N. Shimizu, G. Wagner, and F. Ruddle (2000)
PNAS
97, 1655-1660
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- Secreted and membrane attractin result from alternative splicing of the human ATRN gene.
- W. Tang, T. M. Gunn, D. F. McLaughlin, G. S. Barsh, S. F. Schlossman, and J. S. Duke-Cohan (2000)
PNAS
97, 6025-6030
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