Thoma S, Hecht U, Kippers A, Botella J, De Vries S, Somerville C
Michigan State University-Department of Energy Plant Research Laboratory, Michigan State University, East Lansing 48824.
Plant Physiol. 1994 May;105(1):35-45. doi: 10.1104/pp.105.1.35.
Nonspecific lipid transfer proteins (LTPs) from plants are characterized by their ability to stimulate phospholipid transfer between membranes in vitro. However, because these proteins are generally located outside of the plasma membrane, it is unlikely that they have a similar role in vivo. As a step toward identifying the function of these proteins, one of several LTP genes from Arabidoposis has been cloned and the expression pattern of the gene has been examined by analysis of the tissue specificity of beta-glucuronidase (GUS) activity in transgenic plants containing LTP promoter-GUS fusions and by in situ mRNA localization. The LTP1 promoter was active early in development in protoderm cells of embryos, vascular tissues, lignified tips of cotyledons, shoot meristem, and stipules. In adult plants, the gene was expressed in epidermal cells of young leaves and the stem. In flowers, expression was observed in the epidermis of all developing influorescence and flower organ primordia, the epidermis of the siliques and the outer ovule wall, the stigma, petal tips, and floral nectaries of mature flowers, and the petal/sepal abscission zone of mature siliques. The presence of GUS activity in guard cells, lateral roots, pollen grains, leaf vascular tissue, and internal cells of stipules and nectaries was not confirmed by in situ hybridizations, supporting previous observations that suggest that the reporter gene is subject to artifactual expression. These results are consistent with a role for the LTP1 gene product in some aspect of secretion or deposition of lipophilic substances in the cell walls of expanding epidermal cells and certain secretory tissues. The LTP1 promoter region contained sequences homologous to putative regulatory elements of genes in the phenylpropanoid biosynthetic pathway, suggesting that the expression of the LTP1 gene may be regulated by the same or similar mechanisms as genes in the phenylpropanoid pathway.
植物中的非特异性脂质转移蛋白(LTPs)的特点是能够在体外刺激膜之间的磷脂转移。然而,由于这些蛋白通常位于质膜之外,它们在体内不太可能具有类似的作用。作为确定这些蛋白功能的第一步,已克隆了拟南芥中几个LTP基因之一,并通过分析含有LTP启动子 - GUS融合体的转基因植物中β - 葡萄糖醛酸酶(GUS)活性的组织特异性以及原位mRNA定位来研究该基因的表达模式。LTP1启动子在胚胎的原表皮细胞、维管组织、子叶木质化尖端、茎尖分生组织和托叶的发育早期具有活性。在成年植物中,该基因在幼叶和茎的表皮细胞中表达。在花中,在所有发育中的花序和花器官原基的表皮、角果的表皮和外珠被壁、柱头、花瓣尖端、成熟花的花蜜腺以及成熟角果的花瓣/萼片脱落区均观察到表达。原位杂交未证实保卫细胞、侧根、花粉粒、叶维管组织以及托叶和蜜腺内部细胞中存在GUS活性,这支持了先前的观察结果,即报告基因存在人为表达。这些结果与LTP1基因产物在扩展的表皮细胞和某些分泌组织的细胞壁中亲脂性物质的分泌或沉积的某些方面发挥作用一致。LTP1启动子区域包含与苯丙烷生物合成途径中基因的假定调控元件同源的序列,这表明LTP1基因的表达可能受与苯丙烷途径中基因相同或相似的机制调控。