University of Cologne, Botanical Institute, Biocenter Cologne, Zülpicher Str. 47B, D-50674 Cologne, Germany.
BMC Plant Biol. 2012 Jan 16;12:8. doi: 10.1186/1471-2229-12-8.
We have studied the impact of carbohydrate-starvation on the acclimation response to high light using Arabidopsis thaliana double mutants strongly impaired in the day- and night path of photoassimilate export from the chloroplast. A complete knock-out mutant of the triose phosphate/phosphate translocator (TPT; tpt-2 mutant) was crossed to mutants defective in (i) starch biosynthesis (adg1-1, pgm1 and pgi1-1; knock-outs of ADP-glucose pyrophosphorylase, plastidial phosphoglucomutase and phosphoglucose isomerase) or (ii) starch mobilization (sex1-3, knock-out of glucan water dikinase) as well as in (iii) maltose export from the chloroplast (mex1-2).
All double mutants were viable and indistinguishable from the wild type when grown under low light conditions, but--except for sex1-3/tpt-2--developed a high chlorophyll fluorescence (HCF) phenotype and growth retardation when grown in high light. Immunoblots of thylakoid proteins, Blue-Native gel electrophoresis and chlorophyll fluorescence emission analyses at 77 Kelvin with the adg1-1/tpt-2 double mutant revealed that HCF was linked to a specific decrease in plastome-encoded core proteins of both photosystems (with the exception of the PSII component cytochrome b559), whereas nuclear-encoded antennae (LHCs) accumulated normally, but were predominantly not attached to their photosystems. Uncoupled antennae are the major cause for HCF of dark-adapted plants. Feeding of sucrose or glucose to high light-grown adg1-1/tpt-2 plants rescued the HCF- and growth phenotypes. Elevated sugar levels induce the expression of the glucose-6-phosphate/phosphate translocator2 (GPT2), which in principle could compensate for the deficiency in the TPT. A triple mutant with an additional defect in GPT2 (adg1-1/tpt-2/gpt2-1) exhibited an identical rescue of the HCF- and growth phenotype in response to sugar feeding as the adg1-1/tpt-2 double mutant, indicating that this rescue is independent from the sugar-triggered induction of GPT2.
We propose that cytosolic carbohydrate availability modulates acclimation to high light in A. thaliana. It is conceivable that the strong relationship between the chloroplast and nucleus with respect to a co-ordinated expression of photosynthesis genes is modified in carbohydrate-starved plants. Hence carbohydrates may be considered as a novel component involved in chloroplast-to-nucleus retrograde signaling, an aspect that will be addressed in future studies.
我们研究了使用拟南芥双突变体在碳水化合物饥饿条件下对高光适应反应的影响,这些双突变体在叶绿体中光合作用产物输出的日和夜间途径中受到严重损害。三磷酸丙糖/磷酸转运蛋白(TPT;tpt-2 突变体)的完全敲除突变体与突变体(i)淀粉生物合成(adg1-1、pgm1 和 pgi1-1;ADP-葡萄糖焦磷酸化酶、质体磷酸葡糖变位酶和磷酸葡萄糖异构酶的缺失)或(ii)淀粉动员(sex1-3、葡聚糖水二激酶缺失)以及(iii)叶绿体中麦芽糖输出(mex1-2)的缺陷发生杂交。
所有双突变体在低光照条件下生长时与野生型无明显区别,但除 sex1-3/tpt-2 外,在高光下生长时均表现出高叶绿素荧光(HCF)表型和生长迟缓。用 adg1-1/tpt-2 双突变体进行的类囊体蛋白免疫印迹、Blue-Native 凝胶电泳和 77 开尔文叶绿素荧光发射分析表明,HCF 与两个光系统的质体编码核心蛋白(除 PSII 成分细胞色素 b559 外)特异性减少有关,而核编码天线(LHCs)正常积累,但主要不与它们的光系统结合。去耦天线是暗适应植物 HCF 的主要原因。将蔗糖或葡萄糖喂养给高光下生长的 adg1-1/tpt-2 植物可挽救 HCF 和生长表型。高糖水平诱导葡萄糖-6-磷酸/磷酸转运蛋白 2(GPT2)的表达,这在原则上可以弥补 TPT 的缺乏。在 gpt2-1 缺失的情况下,三重突变体(adg1-1/tpt-2/gpt2-1)对糖喂养的 HCF 和生长表型的恢复与 adg1-1/tpt-2 双突变体相同,表明这种恢复与糖触发的 GPT2 诱导无关。
我们提出,细胞溶质碳水化合物可用性调节拟南芥对高光的适应。可以想象,在碳水化合物饥饿的植物中,叶绿体和细胞核之间关于光合作用基因协调表达的强烈关系可能会发生改变。因此,碳水化合物可以被认为是参与叶绿体到细胞核逆行信号转导的一种新成分,这将是未来研究的一个方面。