Department of Genetics, Faculty of Sciences and Informatics, University of Szeged, H-6726 Szeged, Hungary.
Institute of Plant Biology, HUN-REN Biological Research Centre, H-6726 Szeged, Hungary.
Cells. 2024 Sep 8;13(17):1503. doi: 10.3390/cells13171503.
Circadian clocks are biochemical timers regulating many physiological and molecular processes according to the day/night cycles. The function of the oscillator relies on negative transcriptional/translational feedback loops operated by the so-called clock genes and the encoded clock proteins. Previously, we identified the small GTPase LIGHT INSENSITIVE PERIOD 1 (LIP1) as a circadian-clock-associated protein that regulates light input to the clock in the model plant . We showed that LIP1 is also required for suppressing red and blue light-mediated photomorphogenesis, pavement cell shape determination and tolerance to salt stress. Here, we demonstrate that LIP1 is present in a complex of clock proteins GIGANTEA (GI), ZEITLUPE (ZTL) and TIMING OF CAB 1 (TOC1). LIP1 participates in this complex via GUANINE EX-CHANGE FACTOR 7. Analysis of genetic interactions proved that LIP1 affects the oscillator via modulating the function of GI. We show that LIP1 and GI independently and additively regulate photomorphogenesis and salt stress responses, whereas controlling cell shape and photoperiodic flowering are not shared functions of LIP1 and GI. Collectively, our results suggest that LIP1 affects a specific function of GI, possibly by altering binding of GI to downstream signalling components.
生物钟是根据昼夜节律调节许多生理和分子过程的生化计时器。振荡器的功能依赖于所谓的时钟基因和编码的时钟蛋白的负转录/翻译反馈环。此前,我们鉴定出小分子 GTPase LIGHT INSENSITIVE PERIOD 1 (LIP1) 作为一种与生物钟相关的蛋白,它调节模型植物中时钟对光的输入。我们表明,LIP1 还需要抑制红光和蓝光介导的光形态发生、 pavement 细胞形状决定和耐盐胁迫。在这里,我们证明 LIP1 存在于时钟蛋白 GIGANTEA (GI)、ZEITLUPE (ZTL) 和 TIMING OF CAB 1 (TOC1) 的复合物中。LIP1 通过鸟嘌呤交换因子 7 参与该复合物。遗传相互作用分析证明,LIP1 通过调节 GI 的功能影响振荡器。我们表明,LIP1 和 GI 独立且累加地调节光形态发生和盐胁迫反应,而控制细胞形状和光周期开花不是 LIP1 和 GI 的共同功能。总的来说,我们的结果表明,LIP1 影响 GI 的特定功能,可能通过改变 GI 与下游信号成分的结合来实现。