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Functional analysis of the Arabidopsis thaliana poly(A) binding protein PAB5 gene promoter in Nicotiana tabacum

机译:烟草中拟南芥poly(A)结合蛋白PAB5基因启动子的功能分析

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摘要

Poly(A) binding (PAB) proteins play an important role in posttranscriptional regulation by stabilizing mRNA and initiating translation in eukaryotes. Previous studies have shown that the expression of PAB5 gene encoding one of the poly(A) binding proteins (PABPs) in Arabidopsis thaliana is restricted to pollen, ovule and early embryogenesis. To investigate the tissue-specific expression of the PAB5 promoter, a series of promoter deletions (from -1,804, -1,653, -1,334, -1,014, -715, -424 and -175 to +185) were fused to the uidA reporter gene (GUS) and transformed into tobacco plants (Nicotiana tabacum L.). The results showed that GUS expression driven by the full-length PAB5 promoter was detected in floral organs (pollen, ovule, anther, stigma) and immature seeds, but not in vegetative tissues (root, stem, leaf) and mature seeds. Deletion analysis of the PAB5 promoter region revealed that promoters longer than -1,334 had the similar GUS expression level in pollen, ovule and immature seeds, whereas further 5' deletions resulted in a considerable reduction in GUS activity. These results indicated that the region between -1,653 and -1,014 was necessary to direct the tissue-specific expression of PAB5 promoter during development.
机译:聚(A)结合(PAB)蛋白通过稳定mRNA和启动真核生物的翻译在转录后调控中发挥重要作用。以前的研究表明,拟南芥中编码一种poly(A)结合蛋白(PABPs)的PAB5基因的表达仅限于花粉,胚珠和早期胚胎发生。为了研究PAB5启动子的组织特异性表达,将一系列启动子缺失(-1,804,-1,653,-1,334,-1,014,-715,-424和-175至+185融合)至uidA报告基因(GUS)并转化为烟草植物(Nicotiana tabacum L.)。结果显示,全长PAB5启动子驱动的GUS表达在花器官(花粉,胚珠,花药,柱头)和未成熟种子中检测到,而在营养组织(根,茎,叶)和成熟种子中未检测到。 PAB5启动子区域的缺失分析表明,长于-1,334的启动子在花粉,胚珠和未成熟种子中具有相似的GUS表达水平,而进一步的5'缺失导致GUS活性大大降低。这些结果表明在-1,653和-1,014之间的区域是指导发育期间PAB5启动子的组织特异性表达所必需的。

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