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Characterization of MYB proteins acting as transcriptional regulatory factors for carrot phenylalanine ammonia-lyase gene (DcPAL3)

机译:MYB蛋白作为胡萝卜苯丙氨酸氨解酶基因(DcPAL3)转录调控因子的表征

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摘要

In suspension-cultured carrot cells, a phenylalanine ammonia-lyase gene, DcPAL3, plays an important role in regulation of anthocyanin synthesis. In the DcPAL3 promoter region, a putative cis-element, box-L, which is committed to the upregulation of promoter activity, has been identified. Here, we isolated DcMYB5 cDNA using yeast one-hybrid screening with box-L as a bait from a cDNA library prepared from cells of a variant cultured cell line constitutively synthesizing anthocyanin. Although expression of DcMYB2, 3, and 4 was observed, all of which were previously isolated by plaque hybridization from a subtracted cDNA library of anthocyanin-synthesizing cells of a normal cultured cell line cultured in medium lacking 2,4-dichlorophenoxyacetic acid, DcMYB5 expression was not observed in cells of the normal cultured cell line; high expression of DcMYB5 was observed in cells of the variant cultured cell line. Although not only DcMYB5 but also DcMYB2, 3, and 4 could bind to the box-L sequence in yeast, DcMYB3 and 5 showed strong transcriptional activation activity for DcPAL3 promoter in carrot protoplasts. These results suggest that DcMYB3 and 5 might play an important role in the upregulation of DcPAL3 promoter activity in the different regulatory paths between the normal and variant cultured cell lines.
机译:在悬浮培养的胡萝卜细胞中,苯丙氨酸氨解酶基因DcPAL3在调节花色苷合成中起重要作用。在DcPAL3启动子区域中,已确定了一个致力于顺式启动子活性上调的顺式元件box-L。在这里,我们使用酵母一杂交筛选以Box-L作为诱饵,从cDNA库中分离DcMYB5 cDNA,该cDNA库由组成型合成花色苷的变异培养细胞系的细胞制备。尽管观察到DcMYB2、3和4的表达,但所有这些都先前通过噬斑杂交从在缺乏2,4-二氯苯氧乙酸的培养基中培养的正常培养细胞系的花色苷合成细胞的cDNA消减文库中分离得到,DcMYB5表达在正常培养的细胞系的细胞中未观察到;在变异培养细胞系的细胞中观察到DcMYB5的高表达。尽管不仅DcMYB5还能与DcMYB2、3和4结合到酵母中的box-L序列上,但DcMYB3和5对胡萝卜原生质体中的DcPAL3启动子显示出很强的转录激活活性。这些结果表明,DcMYB3和5在正常和变异培养细胞系之间不同调控途径中的DcPAL3启动子活性上调中可能起重要作用。

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