Sreenivasulu Nese, Altschmied Lothar, Radchuk Volodymyr, Gubatz Sabine, Wobus Ulrich, Weschke Winfriede
Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK), Correnstrasse 3, D-06466 Gatersleben, Germany.
Plant J. 2004 Feb;37(4):539-53. doi: 10.1046/j.1365-313x.2003.01981.x.
Different aspects of barley grain development have been studied in detail, but a more global analysis of gene expression patterns is still missing. We have employed macro arrays, containing 1184 unique sequences from 1421 barley cDNA fragments, to study gene expression profiles in maternal and filial tissues of developing barley caryopses from fertilization to early storage phase. Principle component analysis (PCA) defined distinct expression networks in the pre-storage (0, 2, and 4 days after flowering (DAF)) and early storage phase (10 and 12 DAF). During an intermediate phase (6 and 8 DAF), PCA visualizes a dramatic re-programming of the transcriptional machinery. In maternal tissues, a large set of protein-mobilizing enzyme mRNAs, together with upregulated lipid-mobilizing enzyme and downregulated reactive oxygen species (ROS)-scavenging enzyme genes, suggests mobilization of stored compounds and programmed cell death (PCD). In the filial tissue fraction, a set of genes highly expressed during the pre-storage phase is involved in growth processes, including cell wall biosynthesis. The data suggest that the necessary UDP-glucose is provided both by sucrose synthase (isoform 3) and an invertase-driven pathway. Further, major developmental changes in pathways producing energy are predicted. A bell-shaped expression profile with a peak during the intermediate phase is characteristic for genes associated with photosynthesis and ATP production. The photosynthesis-determined increase of ATP concentration could be a prerequisite for the initiation of grain filling, dominated by starch and storage protein synthesis. Storage product accumulation is accompanied by high transcriptional activity of genes involved in glycolysis and fermentation, as well as in the citric acid cycle.
大麦籽粒发育的不同方面已得到详细研究,但对基因表达模式的更全面分析仍缺失。我们使用了包含1421个大麦cDNA片段中的1184个独特序列的宏阵列,来研究从受精到早期储存阶段发育中的大麦颖果的母体和子代组织中的基因表达谱。主成分分析(PCA)确定了储存前(开花后0、2和4天(DAF))和早期储存阶段(10和12 DAF)的不同表达网络。在中间阶段(6和8 DAF),PCA显示转录机制发生了剧烈的重新编程。在母体组织中,大量动员蛋白质的酶mRNA,以及上调的动员脂质的酶和下调的活性氧(ROS)清除酶基因,表明储存化合物的动员和程序性细胞死亡(PCD)。在子代组织部分,一组在储存前阶段高度表达的基因参与生长过程,包括细胞壁生物合成。数据表明,所需的UDP-葡萄糖由蔗糖合酶(异构体3)和转化酶驱动的途径提供。此外,预测了产生能量的途径中的主要发育变化。与光合作用和ATP产生相关的基因具有在中间阶段达到峰值的钟形表达谱。光合作用决定的ATP浓度增加可能是启动以淀粉和储存蛋白合成为主的籽粒灌浆的先决条件。储存产物的积累伴随着参与糖酵解、发酵以及柠檬酸循环的基因的高转录活性。