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Organ-specific and Agamous-regulated expression and glycosylation of a pollen tube growth-promoting protein.

机译:器官特异性和无性调节的花粉管生长促进蛋白的表达和糖基化。

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摘要

Transmitting tissue-specific (TTS) protein is a pollen tube growth-promoting and attracting glycoprotein located in the stylar transmitting tissue extracellular matrix of the pistil of tobacco. The TTS protein backbones have a deduced molecular mass of about 28 kDa, whereas the glycosylated stylar TTS proteins have apparent molecular masses ranging between 50 and 100 kDa. TTS mRNAs and proteins are ectopically produced in transgenic tobacco plants that express either a cauliflower mosaic virus (CaMV) 35S promoter-TTS2 transgene or a CaMV 35S-promoter-NAG1 (NAG1 = Nicotiana tabacum Agamous gene) transgene. However, the patterns of TTS mRNA and protein accumulation and the quality of the TTS proteins produced are different in these two types of transgenic plants. In 35S-TTS transgenic plants, TTS mRNAs and proteins accumulate constitutively in vegetative and floral tissues. However, the ectopically expressed TTS proteins in these transgenic plants accumulate as underglycosylated protein species with apparent molecular masses between 30 and 50 kDa. This indicates that the capacity to produce highly glycosylated TTS proteins is restricted to the stylar transmitting tissue. In 35S-NAG transgenic plants, NAG1 mRNAs accumulate constitutively in vegetative and floral tissues, and TTS mRNAs are induced in the sepals of these plants. Moreover, highly glycosylated TTS proteins in the 50- to 100-kDa molecular mass range accumulate in the sepals of these transgenic, 35S-NAG plants. These results show that the tobacco NAGI gene, together with other yet unidentified regulatory factors, control the expression of TTS genes and the cellular capacity to glycosylate TTS proteins, which are normally expressed very late in the pistil developmental pathway and function in the final stage of floral development. The sepals in the transgenic 35S-NAG plants also support efficient pollen germination and tube growth, similar to what normally occurs in the pistil, and this ability correlates with the accumulation of the highest levels of the 50- to 100-kDa glycosylated TTS proteins.
机译:传输组织特异性(TTS)蛋白是一种花粉管,可促进和吸引糖蛋白的生长,并位于烟草雌蕊的花粉传输组织胞外基质中。 TTS蛋白骨架的推导分子量约为28 kDa,而糖基化的硬脂酸酯TTS蛋白的表观分子量约为50至100 kDa。 TTS mRNA和蛋白在表达花椰菜花叶病毒(CaMV)35S启动子-TTS2转基因或CaMV 35S-promoter-NAG1(NAG1 =烟草烟无性基因)转基因的转基因烟草植物中异位产生。但是,在这两种类型的转基因植物中,TTS mRNA和蛋白质积累的模式以及产生的TTS蛋白的质量是不同的。在35S-TTS转基因植物中,TTS mRNA和蛋白质在营养和花卉组织中组成性积累。然而,在这些转基因植物中异位表达的TTS蛋白累积为糖基化不足的蛋白种类,其表观分子量在30至50kDa之间。这表明产生高度糖基化的TTS蛋白的能力仅限于柱状传递组织。在35S-NAG转基因植物中,NAG1 mRNA在营养和花卉组织中组成性积累,而TTS mRNA在这些植物的萼片中被诱导。此外,在这些转基因的35S-NAG植物的萼片中积累了50至100 kDa分子量范围的高度糖基化的TTS蛋白。这些结果表明,烟草NAGI基因与其他尚未确定的调节因子共同控制TTS基因的表达和糖基化TTS蛋白的细胞能力,这些蛋白通常在雌蕊发育途径的后期表达,并在雌性激素的最终阶段发挥作用。花的发育。转基因35S-NAG植物中的萼片还支持有效的花粉萌发和试管生长,类似于雌蕊通常发生的情况,并且这种能力与50至100 kDa糖基化TTS蛋白的最高水平的积累相关。

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