Shabrangy Azita, Roustan Valentin, Reipert Siegfried, Weidinger Marieluise, Roustan Pierre-Jean, Stoger Eva, Weckwerth Wolfram, Ibl Verena
Department of Ecogenomics and Systems Biology, University of Vienna, Vienna, Austria.
Core Facility Cell Imaging and Ultrastructure Research, University of Vienna, Vienna, Austria.
Front Plant Sci. 2018 Jun 13;9:775. doi: 10.3389/fpls.2018.00775. eCollection 2018.
(barley) hordoindolines (HINs), HINa, HINb1, and HINb2, are orthologous proteins of wheat puroindolines (PINs) that are small, basic, cysteine-rich seed-specific proteins and responsible for grain hardness. Grain hardness is, next to its protein content, a major quality trait. In barley, is most highly expressed in the mid-stage developed endosperm and is associated with both major endosperm texture and grain hardness. However, data required to understand the spatio-temporal dynamics of transcripts and HIN protein regulation during grain filling processes are missing. Using reverse transcription quantitative PCR (RT-qPCR) and proteomics, we analyzed transcript and HIN protein abundance from whole seeds (WSs) at four [6 days after pollination (dap), 10, 12, and ≥20 dap] as well as from aleurone, subaleurone, and starchy endosperm at two (12 and ≥20 dap) developmental stages. At the WS level, results from RT-qPCR, proteomics, and western blot showed a continuous increase of transcript and HIN protein abundance across these four developmental stages. Miroscopic studies revealed HIN localization mainly at the vacuolar membrane in the aleurone, at protein bodies (PBs) in subaleurone and at the periphery of starch granules in the starchy endosperm. Laser microdissetion (LMD) proteomic analyses identified HINb2 as the most prominent HIN protein in starchy endosperm at ≥20 dap. Additionally, our quantification data revealed a poor correlation between transcript and protein levels of HINs in subaleurone during development. Here, we correlated data achieved by RT-qPCR, proteomics, and microscopy that reveal different expression and localization pattern of HINs in each layer during barley endosperm development. This indicates a contribution of each tissue to the regulation of HINs during grain filling. The effect of the high protein abundance of HINs in the starchy endosperm and their localization at the periphery of starch granules at late development stages at the cereal-based end-product quality is discussed. Understanding the spatio-temporal regulated HINs is essential to improve barley quality traits for high end-product quality, as hard texture of the barley grain is regulated by the ratio between HINb/HINa.
(大麦)大麦吲哚啉(HINs),即HINa、HINb1和HINb2,是小麦麦胚吲哚啉(PINs)的直系同源蛋白,PINs是一类小的、碱性的、富含半胱氨酸的种子特异性蛋白,负责控制籽粒硬度。籽粒硬度是仅次于蛋白质含量的主要品质性状。在大麦中,HINs在发育中期的胚乳中表达量最高,且与胚乳质地和籽粒硬度均有关联。然而,目前尚缺乏了解籽粒灌浆过程中HINs转录本和HIN蛋白调控的时空动态所需的数据。我们使用逆转录定量PCR(RT-qPCR)和蛋白质组学技术,分析了四个发育阶段[授粉后6天(dap)、10天、12天和≥20天]全种子(WSs)以及两个发育阶段(12天和≥20天)糊粉层、亚糊粉层和淀粉胚乳中的HINs转录本和HIN蛋白丰度。在全种子水平上,RT-qPCR、蛋白质组学和蛋白质印迹的结果表明,在这四个发育阶段中,HINs转录本和HIN蛋白丰度持续增加。显微镜研究显示,HINs主要定位于糊粉层的液泡膜、亚糊粉层的蛋白体(PBs)以及淀粉胚乳中淀粉颗粒的周边。激光显微切割(LMD)蛋白质组学分析确定HINb2是≥20天发育阶段淀粉胚乳中最主要的HIN蛋白。此外,我们的定量数据显示,发育过程中亚糊粉层中HINs的转录本水平与蛋白水平之间的相关性较差。在这里,我们将RT-qPCR、蛋白质组学和显微镜观察获得的数据进行关联,这些数据揭示了大麦胚乳发育过程中各层中HINs不同的表达和定位模式。这表明每个组织在籽粒灌浆过程中对HINs的调控都有贡献。本文还讨论了淀粉胚乳中HINs的高蛋白质丰度及其在发育后期淀粉颗粒周边的定位对谷物最终产品品质的影响。了解HINs的时空调控对于改善大麦品质性状以获得高端产品品质至关重要,因为大麦籽粒的硬质地是由HINb/HINa的比例调控的。