Genetical Research



Targeted reduction of the DNA methylation level with 5-azacytidine promotes excision of the medaka fish Tol2 transposable element


ATSUO IIDA a1, ATSUKO SHIMADA a2, AKIHIRO SHIMA a3p1, NAOFUMI TAKAMATSU a1, HIROSHI HORI a1, KOSEI TAKEUCHI a1p2 and AKIHIKO KOGA a1c1
a1 Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan
a2 Department of Biological Sciences, Graduate School of Sciences, University of Tokyo, Tokyo 113-0033, Japan
a3 Department of Integrated Biosciences, Graduate School of Frontier Sciences, University of Tokyo, Kashiwa 277-8562, Japan

Article author query
iida a   [PubMed][Google Scholar] 
shimada a   [PubMed][Google Scholar] 
shima a   [PubMed][Google Scholar] 
takamatsu n   [PubMed][Google Scholar] 
hori h   [PubMed][Google Scholar] 
takeuchi k   [PubMed][Google Scholar] 
koga a   [PubMed][Google Scholar] 

Abstract

The Tol2 element of the medaka fish Oryzias latipes is a member of the hAT (hobo/Activator/Tam3) transposable element family. There is evidence for rapid expansion in the genome and throughout the species in the past but a high spontaneous transposition rate is not observed with current fish materials, suggesting that the Tol2 element and its host species have already acquired an interactive mechanism to control the transposition frequency. DNA methylation is a possible contributing factor, given its involvement with many other transposable elements. We therefore soaked embryos in 5-azacytidine, a reagent that causes reduction in the DNA methylation level, and examined amounts of PCR products reflecting the somatic excision frequency, obtaining direct evidence that exposure promotes Tol2 excision. Our results thus suggest that methylation of the genome DNA is a factor included in the putative mechanisms of control of transposition of the Tol2 element.

(Received January 12 2006)
(Revised March 20 2006)


Correspondence:
c1 Fax: +81 52 789 2974 e-mail: koga@bio.nagoya-u.ac.jp
p1 Present address: Institute for Environmental Sciences, Rokkasho, Aomori 039-3212, Japan.
p2 Present address: Laboratory for Neuronal Circuit, KAN Research Institute, Kyoto 600-8815, Japan.


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