Max Planck Institute of Molecular Plant Physiology, Potsdam-Golm 14476, Germany.
School of Life Sciences, University of Essex, Colchester CO4 3SQ, UK.
Plant Physiol. 2022 Aug 1;189(4):2332-2356. doi: 10.1093/plphys/kiac226.
Many plants, including Arabidopsis (Arabidopsis thaliana), accumulate starch in the daytime and remobilize it to support maintenance and growth at night. Starch accumulation is increased when carbon is in short supply, for example, in short photoperiods. Mobilization is paced to exhaust starch around dawn, as anticipated by the circadian clock. This diel pattern of turnover is largely robust against loss of day, dawn, dusk, or evening clock components. Here, we investigated diel starch turnover in the triple circadian clock mutant lhy cca1 elf3, which lacks the LATE ELONGATED HYPOCOTYL and the CIRCADIAN CLOCK-ASSOCIATED1 (CCA1) dawn components and the EARLY FLOWERING3 (ELF3) evening components of the circadian clock. The diel oscillations of transcripts for the remaining clock components and related genes like REVEILLE and PHYTOCHROME-INTERACING FACTOR family members exhibited attenuated amplitudes and altered peak time, weakened dawn dominance, and decreased robustness against changes in the external light-dark cycle. The triple mutant was unable to increase starch accumulation in short photoperiods. However, it was still able to pace starch mobilization to around dawn in different photoperiods and growth irradiances and to around 24 h after the previous dawn in T17 and T28 cycles. The triple mutant was able to slow down starch mobilization after a sudden low-light day or a sudden early dusk, although in the latter case it did not fully compensate for the lengthened night. Overall, there was a slight trend to less linear mobilization of starch. Thus, starch mobilization can be paced rather robustly to dawn despite a major disruption of the transcriptional clock. It is proposed that temporal information can be delivered from clock components or a semi-autonomous oscillator.
许多植物,包括拟南芥(Arabidopsis thaliana),在白天积累淀粉,晚上再将其重新利用以支持维持和生长。例如,在短光照期,当碳源短缺时,淀粉的积累会增加。动员的速度是为了在黎明时分耗尽淀粉,这与生物钟的昼夜节律相吻合。这种昼夜淀粉周转模式在很大程度上不受失去白天、黎明、黄昏或晚上时钟组件的影响。在这里,我们研究了三重生物钟突变体 lhy cca1 elf3 的昼夜淀粉周转,该突变体缺乏晚期伸长的 Hypocotyl 和生物钟相关的 1 (CCA1)黎明成分以及 EARLY FLOWERING3 (ELF3)的傍晚成分。剩余时钟组件的昼夜转录物的振荡及其相关基因(如 REVEILLE 和 PHYTOCHROME-INTERACING FACTOR 家族成员)的振幅减弱,峰值时间改变,黎明优势减弱,对外部光-暗循环变化的稳健性降低。三重突变体不能在短光照期增加淀粉的积累。然而,它仍然能够在不同的光照期和生长辐照度下,以及在 T17 和 T28 循环中前一个黎明后的 24 小时左右,将淀粉动员到大约黎明时分。三重突变体能够在突然的低光照日或突然的早黄昏后减缓淀粉动员速度,尽管在后一种情况下,它不能完全补偿延长的夜晚。总的来说,淀粉动员的趋势是稍微不那么线性。因此,尽管转录时钟受到严重干扰,但淀粉动员仍能相当稳健地进行到黎明时分。据推测,时间信息可以从时钟组件或半自主振荡器传递。