首页> 外文期刊>Journal of Agricultural and Food Chemistry >Selected Carbohydrate Metabolism Genes Show Coincident Expression Peaks in Grains of In Vitro-Cultured Immature Spikes of Wheat (Triticum aestivum L.)
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Selected Carbohydrate Metabolism Genes Show Coincident Expression Peaks in Grains of In Vitro-Cultured Immature Spikes of Wheat (Triticum aestivum L.)

机译:选定的碳水化合物代谢基因在小麦(Triticum aestivum L.)体外培养的未成熟穗粒中显示出一致的表达峰

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An in vitro culture system is useful to study grain development under defined conditions to minimize confounding effects associated with whole plant studies and metabolite movement into the developing grains. The objective of this study was to monitor the expression patterns of carbohydrate metabolism genes during grain development in an in vitro wheat spike culture, system, immature spikes were cultured prior to anthesis, and grains were collected at various days postanthesis (DPA). Grains from cultured spikes showed maximum expression of starch metabolic genes by 10 DPA, with a rapid decline thereafter. The rapid increase and decrease in expression rate in the in vitro system was thought to be due to fructan exohydrolase (1-FEH and 6-FEH) or sucrose transporter 1 (SUT1) and sucrose synthase (SuSy) genes being highly expressed. SUT1 reached peak expression at 8 DPA, two days earlier than the other genes, and may account for the rapid early stage trigger in expression of the other genes. However, expression of 1-FEH and 6-FEH genes in in vitro-cultured spikes peaked at 12 DPA, two days later than the other genes, and could indicate that fructan catabolism was not a factor in the rapid accumulation of starch in the in vitro-cultured spikes. Accumulation of GBSSI polypeptides generally showed similar patterns in both systems, with the maximum amount in the in vitro system observed four days later than in the in planta spikes, reflecting different turnover controls of GBSSI transcripts. The in vitro system offers opportunities for further refinement and detailed grain development studies.
机译:体外培养系统可用于在规定条件下研究谷物发育,以最大程度降低与整株植物研究相关的混杂影响以及代谢物向发育中谷物的移动。这项研究的目的是在体外小麦穗培养,系统中监测谷物发育过程中碳水化合物代谢基因的表达模式,在花期前培养未成熟的穗,并在花后多天(DPA)收集谷物。培养的穗状花序的谷物在10 DPA时显示出淀粉代谢基因的最大表达,此后迅速下降。在体外系统中表达速率的快速增加和降低被认为是由于果聚糖外切水解酶(1-FEH和6-FEH)或蔗糖转运蛋白1(SUT1)和蔗糖合酶(SuSy)基因的高度表达。 SUT1在8 DPA达到峰值表达,比其他基因提前两天,并且可能解释了其他基因表达的快速早期触发。然而,在体外培养的穗状花序中,1-FEH和6-FEH基因的表达达到峰值,比其他基因晚两天,达到12 DPA,这可能表明果聚糖分解代谢不是淀粉快速积累的因素。体外培养的穗状花序。 GBSSI多肽的积累通常在两个系统中都显示出相似的模式,在体外系统中观察到的最大量比在植物高峰中晚了四天,这反映了GBSSI转录本的不同更新控制。体外系统为进一步完善和详细的谷物发育研究提供了机会。

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