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首页> 外文期刊>Journal of Plant Research >Identification and characterization of genes induced for anthocyanin synthesis and chlorophyll degradation in regenerated torenia shoots using suppression subtractive hybridization, cDNA microarrays, and RNAi techniques
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Identification and characterization of genes induced for anthocyanin synthesis and chlorophyll degradation in regenerated torenia shoots using suppression subtractive hybridization, cDNA microarrays, and RNAi techniques

机译:使用抑制消减杂交,cDNA微阵列和RNAi技术鉴定和表征再生的肾上腺花青素合成和叶绿素降解诱导的基因

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摘要

Anthocyanin synthesis and chlorophyll degradation in regenerated torenia (Torenia fournieri Linden ex Fourn.) shoots induced by osmotic stress with 7% sucrose were examined to identify the genes regulating the underlying molecular mechanism. To achieve this, suppression subtractive hybridization was performed to enrich the cDNAs of genes induced in anthocyanin-synthesizing and chlorophyll-degrading regenerated shoots. The nucleotide sequences of 1,388 random cDNAs were determined, and these were used in the preparation of cDNA microarrays for high-throughput screening. From 1,056 cDNAs analyzed in the microarrays, 116 nonredundant genes were identified, which were up regulated by 7% sucrose to induce anthocyanin synthesis and chlorophyll degradation in regenerated shoots. Of these, eight genes were selected and RNAi transformants prepared, six of which exhibited anthocyanin synthesis inhibition and/or chlorophyll degradation in their leaf discs. Notably, the RNAi transformants of the glucose 6-phosphate/phosphate translocator gene displayed inhibition both of anthocyanin synthesis and chlorophyll degradation in both leaf discs and regenerated shoots. There was also less accumulation of anthocyanin in the petals, and flowering time was shortened. The genes we identified as being up-regulated in the regenerated torenia shoots may help further elucidate the molecular mechanism underlying the induction of anthocyanin synthesis and chlorophyll degradation.
机译:研究了用7%蔗糖渗透压诱导的再生肾上腺(Torenia fournieri Linden ex Fourn。)芽中的花色苷合成和叶绿素降解,以鉴定调节潜在分子机制的基因。为了达到这个目的,进行抑制消减杂交以富集花青素合成和叶绿素降解再生芽中诱导的基因的cDNA。确定了1,388个随机cDNA的核苷酸序列,并将其用于制备cDNA微阵列以进行高通量筛选。从微阵列中分析的1,056个cDNA中,鉴定出116个非冗余基因,这些基因被7%蔗糖上调以诱导花青素合成和再生芽中的叶绿素降解。其中,选择了8个基因并制备了RNAi转化体,其中6个在其叶盘中表现出花青素合成抑制和/或叶绿素降解。值得注意的是,葡萄糖6-磷酸/磷酸转运蛋白基因的RNAi转化子在叶盘和再生芽中均显示出对花色苷合成和叶绿素降解的抑制作用。花瓣中的花色苷含量也较少,并且开花时间缩短了。我们确定在再生的肾小球芽中被上调的基因可能有助于进一步阐明花色苷合成和叶绿素降解诱导的分子机制。

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