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首页> 外文期刊>Russian Journal of Plant Physiology >Cloning and characterization of uridine diphosphate glucose dehydrogenase gene from Ipomoea batatas.
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Cloning and characterization of uridine diphosphate glucose dehydrogenase gene from Ipomoea batatas.

机译:番薯尿苷二磷酸葡萄糖葡萄糖脱氢酶基因的克隆与鉴定。

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摘要

In order to study the structure and expression patterns of uridine diphosphate glucose dehydrogenase (UDPGH) genes in Ipomoea batatas, the transcriptome database of this plant constructed in our lab was first analyzed to screen UDPGH contigs. It was found that there were 23 UDPGH contigs of different sizes in the transcriptome database. Primers were designed to amplify the coding regions of UDPGH, and five UDPGH-coding genes (named IbUDPGH1-IbUDPGH5) were cloned and sequenced. Open reading frames of all the UDPGH were 1443 bp in length, and their identity was more than 97 and 99% at the nucleotide and protein level, respectively. Homology comparison among different plant UDPGH showed that the identity ranged from 73 to 95% at the nucleotide level and from 84 to 95% at the protein level. The results of digital gene expression profile analysis (DGE) displayed that IbUDPGH1 had the highest expression in the tuberous roots, lower in the young and mature leaves, and the lowest in stems and fibrous roots, while IbUDPGH2 and IbUDPGH5 had the highest transcript level in stems, lower in roots, and very low in leaves. The rest genes were expressed at a low level in different tissues. Semi-quantitative RT-PCR results were similar to above data from the DGE. These results imply that the high expression of UDPGH might make large contribution to the accumulation of cell wall polysaccharides in sweet potato stems and roots.
机译:为了研究番薯(Ipomoea batatas)尿苷二磷酸葡萄糖脱氢酶(UDPGH)基因的结构和表达模式,首先分析了我们实验室构建的该植物的转录组数据库,以筛选UDPGH重叠群。发现转录组数据库中存在23个不同大小的UDPGH重叠群。设计引物以扩增UDPGH的编码区,并克隆了五个UDPGH编码基因(命名为IbUDPGH1-IbUDPGH5)并测序。所有UDPGH的开放阅读框长度为1443 bp,在核苷酸和蛋白质水平上它们的同一性分别超过97%和99%。不同植物UDPGH之间的同源性比较表明,同一性在核苷酸水平上为73-95%,在蛋白质水平上为84-95%。数字基因表达谱分析(DGE)结果显示,IbUDPGH1在结节状根中表达最高,在幼叶和成熟叶中较低,茎和纤维根中最低,而IbUDPGH2和IbUDPGH5的转录水平最高。茎,根低,叶低。其余基因在不同组织中低水平表达。半定量RT-PCR结果与DGE的上述数据相似。这些结果暗示UDPGH的高表达可能对甘薯茎和根中细胞壁多糖的积累起很大的作用。

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