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Existence of host-related DNA sequences in the schistosome genome

Published online by Cambridge University Press:  06 April 2009

Y. Iwamura
Affiliation:
Institute of Basic Medical Sciences, University of Tsukuba, Tsukuba-shi, Ibaraki 305, Japan
Y. Irie
Affiliation:
Institute of Basic Medical Sciences, University of Tsukuba, Tsukuba-shi, Ibaraki 305, Japan
R. Kominami
Affiliation:
School of Medicine, Niigata University, Niigata-shi, Niigata 951, Japan
T. Nara
Affiliation:
Institute of Basic Medical Sciences, University of Tsukuba, Tsukuba-shi, Ibaraki 305, Japan
K. Yasuraoka
Affiliation:
Institute of Basic Medical Sciences, University of Tsukuba, Tsukuba-shi, Ibaraki 305, Japan

Extract

DNA sequences homologous to the mouse intracisternal A particle and endogenous type C retrovirus were detected in the DNAs of Schistosoma japonicum adults and S. mansoni eggs. Furthermore, other kinds of repetitive sequences in the host genome such as mouse type 1 Alu sequence (B1), mouse type 2 Alu sequence (B2) and mo-2 sequence, a mouse mini-satellite, were also detected in the DNAs from adults and eggs of S. japonicum and eggs of S. mansoni. Almost all of the sequences described above were absent in the DNAs of S. mansoni adults. The DNA fingerprints of schistosomes, using the mo-2 sequence, were indistinguishable from each other and resembled those of their murine hosts. Moreover, the mo-2 sequence was hypermethylated in the DNAs of schistosomes and its amount was variable in them. These facts indicate that host-related sequences are actually present in schistosomes and that the mo-2 repetitive sequence exists probably in extra-chromosome.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1991

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References

Buetti, E. & Diggelmann, H. (1981). Cloned mouse mammary tumor virus DNA is biologically active in transfected mouse cells and its expression is stimulated by glucocorticoid hormones. Cell 23, 335–45.CrossRefGoogle ScholarPubMed
Cole, M. D., Ono, M. & Huang, R. C. C. (1981). Terminally redundant sequences in cellular intracisternal A-particle genes. Journal of Virology 38, 680–7.Google Scholar
Dobrzanski, P. B. F., Hoeveler, A. & Doereler, W. (1988). Inactivation by sequence-specific methylations of adenovirus promoters in a cell-free transcription system. Journal of Virology 62, 3941–6.CrossRefGoogle Scholar
Dresden, M. H. & Payne, D. C. (1981). A sieving method for the collection of schistosome eggs from mouse intestines. Journal of Parasitology 67, 450–2.CrossRefGoogle Scholar
Jeffreys, A. J., Neumann, R. & Wilson, V. (1990). Repeat unit sequence variation in minisatellites: A novel source of DNA polymorphism for studying variation and mutation by single molecule analysis. Cell 60, 473–85.CrossRefGoogle ScholarPubMed
Jeffreys, A. J., Wilson, V. & Thein, S. L. (1985). Individual-specific ‘fingerprints’ of human DNA. Nature, London 316, 76–9.CrossRefGoogle ScholarPubMed
Khan, A. S., Rowe, W. P. & Martin, M. A. (1982). Cloning of endogenous murine leukemia virus-related sequences from chromosomal DNA of Balb/c and AKR/J mice: Identification of an env progenitor of AKR-247 mink cell focus-forming proviral DNA. Journal of Virology 44, 625–36.CrossRefGoogle ScholarPubMed
Kominami, R., Muramatsu, M. & Moriwaki, K. (1983). A mouse type 2 Alu sequence (M2) is mobile in the genome. Nature, London 301, 87–9.CrossRefGoogle ScholarPubMed
Kominami, R., Takahashi, Y. & Mitani, K. (1989). Chromosomal location of a parental implinting domain. Mouse Newsletter 85, 85.Google Scholar
Kominami, R., Urano, Y., Mishima, Y. & Muramatsu, M. (1981). Organization of ribosomal RNA gene repeats of the mouse. Nucleic Acids Research 9, 3219–33.Google Scholar
Maniatis, T., Fritsch, E. F. & Sambrook, J. (1982). Molecular Cloning: A Laboratory Manual. New York: Cold Spring Harbor Laboratory.Google Scholar
Nara, T., Iwamura, Y., Tanaka, M., Irie, Y. & Yasuraoka, K. (1990). Dynamic changes of DNA sequences in Schistosoma mansoni in the course of development. Parasitology 100, 241–5.CrossRefGoogle ScholarPubMed
Ngernprasirtsiri, J., Kobayashi, H. & Akazawa, T. (1988). DNA methylation as mechanism of transcriptional regulation in nonphotosynthetic plastids in plant cells. Proceedings of the National Academy of Sciences, USA 85, 4750–4.CrossRefGoogle ScholarPubMed
Schmid, C. W. & Jelinek, W. R. (1982). The Alu family of dispersed repetitive sequences. Science 216, 1065–70.CrossRefGoogle ScholarPubMed
Simpson, A. J. G., Sher, A. & McCutchan, T. F. (1982). The genome of Schistosoma mansoni: Isolation of DNA, its size, bases and repetitive sequences. Molecular and Biochemical Parasitology 6, 125–37.CrossRefGoogle ScholarPubMed
Smithers, S. R. & Terry, R. J. (1965). The infection of laboratory hosts with cercariae of Schistosoma mansoni and the recovery of adult worms. Parasitology 55, 695700.Google Scholar
Smithers, S. R., Terry, R. J. & Hockley, D. J. (1969). Host antigens in schistosomiasis. Proceedings of the Royal Society of London, B 171, 483–93.Google ScholarPubMed
Southern, E. M. (1975). Detection of specific sequences among DNA fragments separated by gel electrophoresis. Journal of Molecular Biology 98, 503–17.Google Scholar
Tanaka, M., Iwamura, Y., Amanuma, H., Irie, Y., Watanabe, M., Watanabe, T., Uchiyama, Y. & Yasuraoka, K. (1989). Integration and expression of murine retrovirus-related sequences in schistosomes. Parasitology 99, 31–8.CrossRefGoogle ScholarPubMed
Vanyushin, B. F., Tkacehva, S. G. & Belozersky, A. N. (1970). Rare bases in animal DNA. Nature, London 225, 948–51.CrossRefGoogle ScholarPubMed