Mason H S, Mullet J E
Department of Biochemistry and Biophysics, Texas A&M University, College Station 77843.
Plant Cell. 1990 Jun;2(6):569-79. doi: 10.1105/tpc.2.6.569.
The expression of vspA and vspB genes encoding soybean vegetative storage proteins was studied during seedling development and in response to water deficit, tissue wounding, and jasmonic acid treatment. vspA and vspB encode VSP-alpha and VSP-beta, 28-kilodalton and 31-kilodalton vacuole-localized polypeptides that are 80% homologous. vspA and vspB mRNAs could be distinguished on RNA blots using 3'-end probes. vspA mRNA was threefold to sevenfold more abundant than vspB mRNA in leaves, about equal expression was observed in stems, and vspB mRNA exceeded vspA in roots. Transcripts were not detected in dry seeds but appeared in intact or excised seedling axes between 12 hr and 24 hr after initiation of imbibition. Both transcripts were highly abundant in the meristematic region of seedling stems and in developing leaves but were rare in mature stems, leaves, and roots. In situ localization showed that vsp transcripts were found throughout the hypocotyl hook but were concentrated in cells associated with the epidermis and vascular bundles. Water deficit caused increased vsp mRNA levels in leaves and stems, which suggests that inhibition of growth necessitates temporary storage of amino acids. Wounding induced primarily vspB mRNA in etiolated seedlings, whereas both vspA and vspB mRNA levels increased in wounded leaves. Jasmonic acid and methyl jasmonate were potent inducers of vsp gene expression in cell cultures, developing axes, leaves, and roots. We hypothesize that jasmonic acid levels modulate vsp mRNA abundance in vivo.
在幼苗发育过程中以及对水分亏缺、组织损伤和茉莉酸处理的响应中,研究了编码大豆营养贮藏蛋白的vspA和vspB基因的表达。vspA和vspB分别编码VSP-α和VSP-β,这两种28千道尔顿和31千道尔顿的液泡定位多肽具有80%的同源性。使用3'端探针可在RNA印迹上区分vspA和vspB mRNA。在叶片中,vspA mRNA的丰度比vspB mRNA高3至7倍,在茎中观察到二者表达量大致相等,而在根中vspB mRNA超过vspA。在干种子中未检测到转录本,但在吸胀开始后12小时至24小时之间,完整或切除的幼苗轴中出现了转录本。两种转录本在幼苗茎的分生组织区域和发育中的叶片中都高度丰富,但在成熟的茎、叶和根中很少见。原位定位显示,vsp转录本遍布下胚轴弯钩,但集中在与表皮和维管束相关的细胞中。水分亏缺导致叶片和茎中vsp mRNA水平升高,这表明生长抑制需要暂时储存氨基酸。损伤主要诱导黄化幼苗中的vspB mRNA,而在受伤叶片中vspA和vspB mRNA水平均升高。茉莉酸和茉莉酸甲酯是细胞培养物、发育中的轴、叶片和根中vsp基因表达的有效诱导剂。我们假设茉莉酸水平在体内调节vsp mRNA的丰度。