Département de Sciences Biologiques, Institut de Recherche en Biologie Végétale, Université de Montréal, 4101 Sherbrooke est, Montreal, Quebec, Canada H1X 2B2.
Plant Physiol. 2014 Feb;164(2):966-77. doi: 10.1104/pp.113.229856. Epub 2013 Dec 13.
Dinoflagellates are microscopic, eukaryotic, and primarily marine plankton. Temporary cyst formation is a well-known physiological response of dinoflagellate cells to environmental stresses. However, the molecular underpinnings of cold-induced cyst physiology have never been described. Cultures of the photosynthetic dinoflagellate Lingulodinium polyedrum readily form temporary cysts when placed at low (8°C±1°C) temperature and excyst to form normal motile cells following a return to normal temperature (18°C±1°C). The normal circadian bioluminescence rhythm and the expected changes in Luciferin Binding Protein abundance were arrested in L. polyedrum cysts. Furthermore, after excystment, the bioluminescence rhythm initiates at a time corresponding to zeitgeber 12, independent of the time when the cells encysted. Phosphoprotein staining after two-dimensional polyacrylamide gel electrophoresis, as well as column-based phosphoprotein enrichment followed by liquid chromatography tandem mass spectrometry, showed cyst proteins are hypophosphorylated when compared with those from motile cells, with the most marked decreases found for predicted Casein Kinase2 target sites. In contrast to the phosphoproteome, the cyst proteome is not markedly different from motile cells, as assessed by two-dimensional polyacrylamide gel electrophoresis. In addition to changes in the phosphoproteome, RNA sequencing revealed that cysts show a significant decrease in the levels of 132 RNAs. Of the 42 RNAs that were identified by sequence analysis, 21 correspond to plastid-encoded gene products and 11 to nuclear-encoded cell wall/plasma membrane components. Our data are consistent with a model in which the highly reduced metabolism in cysts is achieved primarily by alterations in the phosphoproteome. The stalling of the circadian rhythm suggests temporary cysts may provide an interesting model to address the circadian system of dinoflagellates.
甲藻是微小的、真核的,主要是海洋浮游生物。临时囊泡形成是甲藻细胞对环境压力的一种众所周知的生理反应。然而,低温诱导囊泡生理学的分子基础从未被描述过。当光合甲藻腰鞭毛虫置于低温(8°C±1°C)时,很容易形成临时囊泡,当温度恢复正常(18°C±1°C)时,囊泡会出囊形成正常的游动细胞。正常的昼夜生物发光节律和预期的荧光素结合蛋白丰度变化在腰鞭毛虫囊泡中被阻断。此外,出囊后,生物发光节律在与 Zeitgeber12 对应的时间开始,与细胞出囊的时间无关。二维聚丙烯酰胺凝胶电泳后的磷酸化蛋白染色,以及基于柱的磷酸化蛋白富集后进行液相色谱串联质谱分析,表明与游动细胞相比,囊泡蛋白的磷酸化程度较低,预测的酪蛋白激酶 2 靶位的减少最为显著。与磷酸蛋白组不同,囊泡蛋白组与游动细胞没有明显差异,这可以通过二维聚丙烯酰胺凝胶电泳来评估。除了磷酸蛋白组的变化外,RNA 测序还表明,囊泡中 132 种 RNA 的水平显著下降。在通过序列分析鉴定的 42 个 RNA 中,21 个对应于质体编码基因产物,11 个对应于核编码细胞壁/质膜成分。我们的数据与一个模型一致,即囊泡中高度还原的代谢主要通过磷酸蛋白组的改变来实现。昼夜节律的停滞表明,临时囊泡可能为解决甲藻的昼夜系统提供一个有趣的模型。