A recombination hotspot in the LTR of a mouse retrotransposon identified in an in vitro system
- PMID: 2544295
- DOI: 10.1016/0092-8674(89)90332-2
A recombination hotspot in the LTR of a mouse retrotransposon identified in an in vitro system
Abstract
The recombinational frequency between two long terminal repeat elements (LTR-IS) of a mouse retrotransposon was about 13 times higher, compared with that of two control DNA sequences in extracts from mouse testes, but not in extracts from ascites cells. Deletion of a 37 bp region from the LTR-IS element strongly suppresses its recombinational activity. This 37 bp region encompasses an area of potentially single-stranded DNA and interacts with at least two nuclear proteins. One of them binds sequence-specifically to single-stranded DNA and is present in both types of extracts. Another protein(s) binds to dsDNA at the motif TGGAAATCCCC and is absent in extracts from testes. Our results suggest that a cis-acting DNA sequence within the 504 bp LTR-IS element is responsible for its high recombinational activity in vitro, and they further support the previous suggestion that the LTR-IS elements are meiotic recombinational hotspots in vivo.
Similar articles
-
Retroviral characteristics of the long terminal repeat of murine E.Tn sequences.EMBO J. 1985 Nov;4(11):2911-5. doi: 10.1002/j.1460-2075.1985.tb04022.x. EMBO J. 1985. PMID: 2998763 Free PMC article.
-
Evidence that a major class of mouse endogenous long terminal repeats (LTRs) resulted from recombination between exogenous retroviral LTRs and similar LTR-like elements (LTR-IS).Proc Natl Acad Sci U S A. 1984 Nov;81(21):6696-700. doi: 10.1073/pnas.81.21.6696. Proc Natl Acad Sci U S A. 1984. PMID: 6093113 Free PMC article.
-
Mouse retrotransposons: a cellular reservoir of long terminal repeat (LTR) elements with diverse transcriptional specificities.Adv Cancer Res. 1991;56:215-51. doi: 10.1016/s0065-230x(08)60482-0. Adv Cancer Res. 1991. PMID: 1851374 Review. No abstract available.
-
A nuclear single-stranded-DNA binding factor interacts with the long terminal repeats of the 1731 Drosophila retrotransposon.J Virol. 1992 Mar;66(3):1682-7. doi: 10.1128/JVI.66.3.1682-1687.1992. J Virol. 1992. PMID: 1371170 Free PMC article.
-
Hotspots of homologous recombination in mouse meiosis.Adv Biophys. 1995;31:119-32. doi: 10.1016/0065-227x(95)99387-5. Adv Biophys. 1995. PMID: 7625269 Review.
Cited by
-
Structural diversity and nuclear protein binding sites in the long terminal repeats of feline leukemia virus.J Virol. 1990 Apr;64(4):1675-82. doi: 10.1128/JVI.64.4.1675-1682.1990. J Virol. 1990. PMID: 2157050 Free PMC article.
-
Formation of novel hairpin structures by telomeric C-strand oligonucleotides.Nucleic Acids Res. 1992 Feb 11;20(3):507-11. doi: 10.1093/nar/20.3.507. Nucleic Acids Res. 1992. PMID: 1741285 Free PMC article.
-
Sequence of cDNA comprising the human pur gene and sequence-specific single-stranded-DNA-binding properties of the encoded protein.Mol Cell Biol. 1992 Dec;12(12):5673-82. doi: 10.1128/mcb.12.12.5673-5682.1992. Mol Cell Biol. 1992. PMID: 1448097 Free PMC article.
-
Mitotic recombination produces the majority of recessive fibroblast variants in heterozygous mice.Proc Natl Acad Sci U S A. 1999 Aug 3;96(16):9230-5. doi: 10.1073/pnas.96.16.9230. Proc Natl Acad Sci U S A. 1999. PMID: 10430925 Free PMC article.
-
Characterization and cloning of p11, a transrepressor of Drosophila melanogaster retrotransposon 1731.Nucleic Acids Res. 1995 Dec 25;23(24):5073-9. doi: 10.1093/nar/23.24.5073. Nucleic Acids Res. 1995. PMID: 8559667 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources