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1 July 2000 Absence of Linkage between Radiosensitivity and the Predisposing Atp7b Gene Mutation for Heritable Hepatitis in the LEC Rat
Toshiaki Ogiu, Mayumi Nishimura, Fumiaki Watanabe, Hideki Ukai, Hiroko Ishii-Ohba, Yoshiya Shimada, Hideo Tsuji, Junko Sakurai, Okio Hino
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Abstract

Ogiu, T., Nishimura, M., Watanabe, F., Ukai, H., Ishii-Ohba, H., Shimada, Y., Tsuji, H., Sakurai, J. and Hino, O. Absence of Linkage between Radiosensitivity and the Predisposing Atp7b Gene Mutation for Heritable Hepatitis in the LEC Rat.

The LEC rat is known to be a mutant strain that spontaneously develops heritable hepatitis due to copper accumulation, caused by mutation of the copper-transporting ATPase gene (Atp7b). Immunodeficiency and radiosensitivity have also been observed. Hayashi et al. extensively examined the radiosensitivity of the LEC rat and concluded that its hypersensitivity is controlled by a single autosomal gene. Furthermore, they suggested the possibility that it correlates to copper accumulation due to the Atp7b gene mutation, because ionizing radiation-induced hydroxyl radicals might act in concert with copper-induced hydroxyl radicals. In the present experiment, we analyzed linkage between radiosensitivity and the mutation responsible for hepatitis in F1 animals of a cross with the F344 rat. Our results clearly demonstrated an absence of any significant association. In addition, partial dominance for radiosensitivity was observed, and radiosensitive (F1 × LEC) backcross rats were twice as numerous as their radioresistant counterparts, suggesting the possibility of control by two or more recessive genes.

Toshiaki Ogiu, Mayumi Nishimura, Fumiaki Watanabe, Hideki Ukai, Hiroko Ishii-Ohba, Yoshiya Shimada, Hideo Tsuji, Junko Sakurai, and Okio Hino "Absence of Linkage between Radiosensitivity and the Predisposing Atp7b Gene Mutation for Heritable Hepatitis in the LEC Rat," Radiation Research 154(1), 113-116, (1 July 2000). https://doi.org/10.1667/0033-7587(2000)154[0113:AOLBRA]2.0.CO;2
Received: 12 October 1999; Accepted: 1 March 2000; Published: 1 July 2000
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