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Hua, Y.*; Narumi, Issei; Gao, G.*; Tian, B.*; Sato, Katsuya; Kitayama, Shigeru; Shen, B.*
Biochemical and Biophysical Research Communications, 306(2), p.354 - 360, 2003/06
Times Cited Count:152 Percentile:95.76(Biochemistry & Molecular Biology)We have identified a unique deinococcal gene, , as a general switch for downstream DNA repair and protection pathways, from a natural mutant, in which is disrupted by a transposon. Complete functional disruption of the gene in wild-type leads to dramatic sensitivity to ionizing radiation. Radioresistance of the disruptant could be fully restored by complementation with . In response to radiation stress, PprI can significantly and specifically induce the gene expression of and and enhance the enzyme activities of catalases. These results strongly suggest that PprI plays a crucial role in regulating multiple DNA repair and protection pathways in response to radiation stress.
Sato, Katsuya; Kikuchi, Masahiro; Narumi, Issei
JAERI-Conf 2002-005, p.172 - 184, 2002/03
a DNA damage response mechanism. However, the damage response is poorly understood in . By investigating the function of deinococcal proteins, we found that, unlike in , LexA is not involved in the regulation of RecA in . This, in turn, led us to speculate that has an alternative DNA damage response mechanism with which to control expression. Recently, we discovered that a novel protein regulates the expression of gene. The novel regulatory protein (designated as PprI) also control the induction of gene following irradiation. Thus, possesses unique mechanisms of DNA damage recognition and repair gene induction.