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Cloning and expression analysis of UpPDS gene in Ulva pertusa

机译:百日草UpPDS基因的克隆与表达分析

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Phytoene desaturase (PDS) is an essential constituent of several carotenoid biosynthetic enzymes, which catalyzes phytoene into zeta-carotenoids. Here, a cDNA encoding PDS gene named UpPDS in Ulva pertusa was cloned by the approaches of expressed sequence tag sequencing of suppression subtractive hybridization cDNA library and rapid amplification of cDNA ends technique. The results showed that the full-length cDNA of UpPDS was 2029 bp, containing 1599 bp open reading frame and encoding 532 amino acids. Homology analysis showed that the deduced UpPDS protein was highly homologous to the PDS proteins from some algal species. Phylogenetic analysis indicated that the UpPDS was clustered together with PDS of Ectocarpus siliculosus firstly and was more close to PDS proteins from Chlamydomonas reinhardtii and Volvox carteri. The RT-qPCR analysis indicated that the transcript level of UpPDS was upregulated during the period of emersion.
机译:番茄红素去饱和酶(PDS)是几种类胡萝卜素生物合成酶的重要组成部分,它们可将八氢番茄红素催化成Zeta类胡萝卜素。在此,通过抑制消减杂交cDNA文库的表达序列标签测序和cDNA末端快速扩增技术,克隆了百日草中编码PDS基因UpPDS的cDNA。结果表明,UpPDS的全长cDNA为2029 bp,含有1599 bp的开放阅读框,编码532个氨基酸。同源性分析表明,推论的UpPDS蛋白与某些藻类物种的PDS蛋白高度同源。系统发育分析表明,UpPDS首先与Ectocarpus siliculosus的PDS聚在一起,并且更接近于莱茵衣藻和沃尔沃卡氏菌的PDS蛋白。 RT-qPCR分析表明,在出苗期,UpPDS的转录水平上调。

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