Molecular cloning of Arabidopsis photolyase gene (PHR1) and characterization of its promoter region

被引:8
|
作者
Sakamoto, A [1 ]
Tanaka, A [1 ]
Watanabe, H [1 ]
Tano, S [1 ]
机构
[1] Japan Atom Energy Res Inst, Adv Sci Res Ctr, Res Grp Plant Genes, Takasaki, Gumma 3701292, Japan
来源
DNA SEQUENCE | 1998年 / 9卷 / 5-6期
关键词
UV damage; DNA repair; cyclobutane pyrimidine dimer; Arabidopsis thaliana;
D O I
10.3109/10425179809008473
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Photolyase is an enzyme that repairs ultraviolet (UV)-damaged DNA by photoreactivation. In higher plants, accumulation of photolyase (PHR1) mRNA is induced by either UV or visible light. In order to know the molecular mechanism by which PHR1 gene expression is induced by light, we have determined the genomic structure and the 5'-flanking sequence of the Arabidopsis PHR1 gene. The PHR1 gene spans approximately 2.5 kb of genomic DNA and consists of 9 exons. In the promoter region of PHX1, there are two pairs of inverted repeats spanning more than sixty base pairs. The promoter also contains DNA motifs similar to the GT-1 box or G-box found in many light-inducible gene promoters. EMSA. analysis showed that several proteins in Arabidopsis nuclear extract bound to the G-box-like motifs. These results raise the possibility that the Arabidopsis PHR1 gene is regulated by transcription factors which interact with these motifs.
引用
收藏
页码:335 / 340
页数:6
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