A sequential program of dual phosphorylation of KaiC as a basis for circadian rhythm in cyanobacteria

被引:180
作者
Nishiwaki, Taeko
Satomi, Yoshinori
Kitayama, Yohko
Terauchi, Kazuki
Kiyohara, Reiko
Takao, Toshifumi
Kondo, Takao [1 ]
机构
[1] Nagoya Univ, Div Biol Sci, Grad Sch Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan
[2] Japan Sci & Technol Agcy, SORST, Chikusa Ku, Nagoya, Aichi 4648602, Japan
[3] Osaka Univ, Inst Prot Res, Suita, Osaka 565, Japan
关键词
circadian rhythm; cyanobacteria; in vitro; KaiC; phosphorylation;
D O I
10.1038/sj.emboj.7601832
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The circadian phosphorylation cycle of the cyanobacterial clock protein KaiC has been reconstituted in vitro. The phosphorylation profiles of two phosphorylation sites in KaiC, serine 431 (S431) and threonine 432 (T432), revealed that the phosphorylation cycle contained four steps: (i) T432 phosphorylation; (ii) S431 phosphorylation to generate the double-phosphorylated form of KaiC; (iii) T432 dephosphorylation; and (iv) S431 dephosphorylation. We then examined the effects of mutations introduced at one KaiC phosphorylation site on the intact phosphorylation site. We found that the product of each step in the phosphorylation cycle regulated the reaction in the next step, and that double phosphorylation converted KaiC from an autokinase to an autophosphatase, whereas complete dephosphorylation had the opposite effect. These mechanisms serve as the basis for cyanobacterial circadian rhythm generation. We also found that associations among KaiA, KaiB, and KaiC result from S431 phosphorylation, and these interactions would maintain the amplitude of the rhythm.
引用
收藏
页码:4029 / 4037
页数:9
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