Insertional mutagenesis in a homologue of a Pi transporter gene confers arsenate resistance on Chlamydomonas

被引:15
作者
Kobayashi, I
Fujiwara, S
Shimogawara, K
Kaise, T
Usuda, H
Tsuzuki, M
机构
[1] Tokyo Univ Pharm & Life Sci, Sch Life Sci, Hachioji, Tokyo 1920395, Japan
[2] Teikyo Univ, Sch Med, Chem Lab, Hachioji, Tokyo 1920395, Japan
关键词
arsenate resistance; Chlamydomonas reinhardtii; Pi transporter; Pi uptake;
D O I
10.1093/pcp/pcg081
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
An arsenate-resistant mutant AR3 of Chlamydomonas reinhardtii is a recessive mutant generated by random insertional mutagenesis using the ARG7 gene. AR3 shows about 10-fold resistance against arsenate toxicity compared with the wild type. By using a flanking region of an inserted tag as a probe, we cloned the corresponding wild-type allele (PTB1) of a mutated gene, which could completely complement the arsenate-resistance phenotype of AR3. The size of PTB1 cDNA is about 6.0 kb and it encodes a putative protein comprising 1,666 amino acid residues. This protein exhibits significant sequence similarity with the yeast Pho89 protein, which is known to be a Na+/Pi co-transporter, although the PTB1 protein carries an additional Gln- and Gly-rich large hydrophilic region in the middle of its primary structure. Analyses of arsenic accumulation and release revealed that PTB1-disrupted cells show arsenate resistance due to low arsenate uptake. These results suggest that the PTB1 protein is a factor involved in arsenate (or Pi) uptake. Kinetics of Pi uptake revealed that the activity of high-affinity Pi transport component in AR3 is more activated than that in the wild type.
引用
收藏
页码:597 / 606
页数:10
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