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Isolation and characterisation of the ADP-glucose pyrophosphorylase small subunit gene (AgpS1) promoter in tomato (Solanum lycopersicum L.).

机译:番茄(Solanum lycopersicum L.)中ADP-葡萄糖焦磷酸化酶小亚基基因(AgpS1)启动子的分离和鉴定。

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摘要

ADP-glucose pyrophosphorylase (AGPase) is a key regulatory enzyme in starch biosynthesis. In this research, 2,885 bp of the predicted promoter sequence for the AgpS1 gene encoding the AGPase small subunit was isolated from tomato. Sequence analyses revealed a number of known cis-elements related to responses to salt and dehydration stress and sugar repression; predicted TATA boxes are located at -88 to -94 bp and -114 to -120 bp. The spatial expression pattern and tissue/organ specificity of AgpS1 were analysed in during development using promoter-GUS transgenic tomato plants. Based on GUS staining, the obtained sequence was proven to be the functional promoter and directed broad expression in both sink and source tissues/organs, including seedling, stem, flower, fruit stalk, fruit and root. In source leaf and early developing fruit, GUS staining was observed in all tissues, except for epidermal tissue. In contrast, GUS staining tended to be confined to vascular tissues in seedling, stem, fruit stalk and ripening fruit. In particular, a patchy staining pattern was observed in the phloem of the stem and fruit stalk, suggesting that AgpS1 is expressed in the phloem companion cells in those organs. These results also suggest that AGPase mainly functions in the vascular tissue of those organs.
机译:ADP-葡萄糖焦磷酸化酶(AGPase)是淀粉生物合成中的关键调节酶。在这项研究中,从番茄中分离了编码AGPase小亚基的AgpS1基因的2885 bp预测启动子序列。序列分析揭示了许多已知的与盐分,脱水胁迫和糖分抑制反应有关的顺式元素。预测的TATA盒位于-88至-94 bp和-114至-120 bp之间。使用启动子-GUS转基因番茄植物,在发育过程中分析了AgpS1的空间表达模式和组织/器官特异性。基于GUS染色,证明所获得的序列是功能启动子,并在包括种子,茎,花,果梗,果实和根的汇和源组织/器官中均定向广泛表达。在源叶和早期发育的果实中,除表皮组织外,所有组织均观察到GUS染色。相反,GUS染色倾向于局限于幼苗,茎,果梗和成熟果实中的维管组织。特别是,在茎和果柄的韧皮部中观察到斑驳的染色模式,这表明AgpS1在那些器官的韧皮部陪伴细胞中表达。这些结果还表明,AGPase主要在那些器官的血管组织中起作用。

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