Xu Xiaodong, Hotta Carlos T, Dodd Antony N, Love John, Sharrock Robert, Lee Young Wha, Xie Qiguang, Johnson Carl H, Webb Alex A R
Department of Biological Sciences, Vanderbilt University, Nashville, Tenessee 37235, USA.
Plant Cell. 2007 Nov;19(11):3474-90. doi: 10.1105/tpc.106.046011. Epub 2007 Nov 2.
Plants have circadian oscillations in the concentration of cytosolic free calcium (Ca(2+)). To dissect the circadian Ca(2+)-signaling network, we monitored circadian Ca(2+) oscillations under various light/dark conditions (including different spectra) in Arabidopsis thaliana wild type and photoreceptor and circadian clock mutants. Both red and blue light regulate circadian oscillations of Ca(2+). Red light signaling is mediated by PHYTOCHROME B (PHYB). Blue light signaling occurs through the redundant action of CRYPTOCHROME1 (CRY1) and CRY2. Blue light also increases the basal level of Ca(2+), and this response requires PHYB, CRY1, and CRY2. Light input into the oscillator controlling Ca(2+) rhythms is gated by EARLY FLOWERING3. Signals generated in the dark also regulate the circadian behavior of Ca(2+). Oscillations of Ca(2+) and CHLOROPHYLL A/B BINDING PROTEIN2 (CAB2) promoter activity are dependent on the rhythmic expression of LATE ELONGATED HYPOCOTYL and CIRCADIAN CLOCK-ASSOCIATED1, but Ca(2+) and CAB2 promoter activity are uncoupled in the timing of cab1 (toc1-1) mutant but not in toc1-2. We suggest that the circadian oscillations of Ca(2+) and CAB2 promoter activity are regulated by distinct oscillators with similar components that are used in a different manner and that these oscillators may be located in different cell types in Arabidopsis.
植物细胞质游离钙(Ca(2+))浓度存在昼夜节律振荡。为剖析昼夜节律性钙信号网络,我们在拟南芥野生型、光受体和生物钟突变体的各种光/暗条件(包括不同光谱)下监测了昼夜节律性Ca(2+)振荡。红光和蓝光均调节Ca(2+)的昼夜节律振荡。红光信号由光敏色素B(PHYB)介导。蓝光信号通过隐花色素1(CRY1)和隐花色素2(CRY2)的冗余作用发生。蓝光还会提高Ca(2+)的基础水平,且该反应需要PHYB、CRY1和CRY2。输入到控制Ca(2+)节律的振荡器中的光由早花3(EARLY FLOWERING3)控制。黑暗中产生的信号也调节Ca(2+)的昼夜节律行为。Ca(2+)振荡和叶绿素A/B结合蛋白2(CAB2)启动子活性依赖于晚伸长下胚轴(LATE ELONGATED HYPOCOTYL)和生物钟相关1(CIRCADIAN CLOCK-ASSOCIATED1)的节律性表达,但在cab1(toc1-1)突变体中Ca(2+)和CAB2启动子活性在时间上解偶联,而在toc1-2中则不然。我们认为,Ca(2+)和CAB2启动子活性的昼夜节律振荡由具有相似组分但使用方式不同的不同振荡器调节,并且这些振荡器可能位于拟南芥的不同细胞类型中。