Fujiki Y, Ito M, Nishida I, Watanabe A
Department of Biological Sciences, Graduate School of Science, University of Tokyo, Bunkyo-ku, Hongo, Tokyo 113-0033, Japan.
Plant Physiol. 2000 Nov;124(3):1139-48. doi: 10.1104/pp.124.3.1139.
We have identified many dark-inducible (din) genes that are expressed in Arabidopsis leaves kept in the dark. In the present study we addressed the question of how plant cells sense the depletion of sugars, and how sugar starvation triggers din gene expression in suspension-cultured cells of Arabidopsis. Depletion of sucrose in the medium triggered marked accumulation of din transcripts. Suppression of din gene expression by 2-deoxy-Glc, and a non-suppressive effect exerted by 3-O-methyl-Glc, suggested that sugar-repressible expression of din genes is mediated through the phosphorylation of hexose by hexokinase, as exemplified in the repression of photosynthetic genes by sugars. We have further shown that the signaling triggered by sugar starvation involves protein phosphorylation and dephosphorylation events, and have provided the first evidence that multiple pathways of protein dephosphorylation exist in sugar starvation-induced gene expression. An inhibitor of serine/threonine protein kinase, K-252a, inhibited din gene expression in sugar-depleted cells. Okadaic acid, which may preferentially inhibit type 2A protein phosphatases over type 1, enhanced the transcript levels of all din genes, except din6 and din10, under sugar starvation. Conversely, a more potent inhibitor of type 1 and 2A protein phosphatases, calyculin A, increased transcripts from din2 and din9, but decreased those from other din genes, in sugar-depleted cells. On the other hand, calyculin A, but not okadaic acid, completely inhibited the gene expression of chlorophyll a/b-binding protein under sugar starvation. These results indicate that multiple signaling pathways, mediated by different types of protein phosphatases, regulate gene expression during sugar starvation.
我们已经鉴定出许多在黑暗中培养的拟南芥叶片中表达的黑暗诱导(din)基因。在本研究中,我们探讨了植物细胞如何感知糖分的耗尽,以及糖饥饿如何触发拟南芥悬浮培养细胞中din基因的表达。培养基中蔗糖的耗尽引发了din转录本的显著积累。2-脱氧葡萄糖对din基因表达的抑制作用,以及3-O-甲基葡萄糖的非抑制作用,表明din基因的糖可抑制表达是通过己糖激酶对己糖的磷酸化介导的,就像糖对光合基因的抑制作用一样。我们进一步表明,糖饥饿引发的信号传导涉及蛋白质磷酸化和去磷酸化事件,并首次提供证据表明在糖饥饿诱导的基因表达中存在多种蛋白质去磷酸化途径。丝氨酸/苏氨酸蛋白激酶抑制剂K-252a抑制了糖耗尽细胞中din基因的表达。冈田酸可能优先抑制2A型蛋白磷酸酶而非1型蛋白磷酸酶,在糖饥饿条件下,它提高了除din6和din10之外所有din基因的转录水平。相反,一种对1型和2A型蛋白磷酸酶更有效的抑制剂花萼海绵诱癌素A,在糖耗尽细胞中增加了din2和din9的转录本,但降低了其他din基因的转录本。另一方面,花萼海绵诱癌素A而非冈田酸,在糖饥饿条件下完全抑制了叶绿素a/b结合蛋白的基因表达。这些结果表明,由不同类型的蛋白磷酸酶介导的多种信号通路在糖饥饿期间调节基因表达。