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首页> 外文期刊>International Journal of Molecular Sciences >De Novo Sequencing and Analysis of the Safflower Transcriptome to Discover Putative Genes Associated with Safflor Yellow in Carthamus tinctorius L.
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De Novo Sequencing and Analysis of the Safflower Transcriptome to Discover Putative Genes Associated with Safflor Yellow in Carthamus tinctorius L.

机译:De Novo测序和红花转录组分析以发现与红花红花相关的推定基因在红花中。

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Safflower (Carthamus tinctorius L.), an important traditional Chinese medicine, is cultured widely for its pharmacological effects, but little is known regarding the genes related to the metabolic regulation of the safflower’s yellow pigment. To investigate genes related to safflor yellow biosynthesis, 454 pyrosequencing of flower RNA at different developmental stages was performed, generating large databases.In this study, we analyzed 454 sequencing data from different flowering stages in safflower. In total, 1,151,324 raw reads and 1,140,594 clean reads were produced, which were assembled into 51,591 unigenes with an average length of 679 bp and a maximum length of 5109 bp. Among the unigenes, 40,139 were in the early group, 39,768 were obtained from the full group and 28,316 were detected in both samples. With the threshold of “log2 ratio ≥ 1”, there were 34,464 differentially expressed genes, of which 18,043 were up-regulated and 16,421 were down-regulated in the early flower library. Based on the annotations of the unigenes, 281 pathways were predicted. We selected 12 putative genes and analyzed their expression levels using quantitative real time-PCR. The results were consistent with the 454 sequencing results. In addition, the expression of chalcone synthase, chalcone isomerase and anthocyanidin synthase, which are involved in safflor yellow biosynthesis and safflower yellow pigment (SYP) content, were analyzed in different flowering periods, indicating that their expression levels were related to SYP synthesis. Moreover, to further confirm the results of the 454 pyrosequencing, full-length cDNA of chalcone isomerase (CHI) and anthocyanidin synthase (ANS) were cloned from safflower petal by RACE (Rapid-amplification of cDNA ends) method according to fragment of the transcriptome.
机译:红花(Carthamus tinctorius L.)是一种重要的传统中药,由于其药理作用而被广泛培养,但关于红花黄色素的代谢调节相关基因的了解很少。为了研究与红花黄生物合成相关的基因,在不同发育阶段对花RNA进行了454次焦磷酸测序,生成了大型数据库。在本研究中,我们分析了红花不同开花阶段的454份测序数据。总共产生了1,151,324个原始读数和1,140,​​594个纯净读数,它们被组装成51,591个单基因,平均长度为679 bp,最大长度为5109 bp。在单基因中,早期组为40,139,完整组为39,768,两个样本中均检测到28,316。在“ log2比≥1”的阈值下,早期花库中有34,464个差异表达基因,其中有18,043个上调而有16,421个下调。基于单基因的注释,预测了281条途径。我们选择了12个推定基因,并使用实时定量PCR分析了它们的表达水平。结果与454测序结果一致。此外,分析了在不同开花期红花黄生物合成和红花黄色素(SYP)含量相关的查尔酮合酶,查尔酮异构酶和花色苷合酶的表达,表明它们的表达水平与SYP合成有关。此外,为进一步证实454焦磷酸测序的结果,根据转录组的片段,通过RACE(cDNA末端的快速扩增)方法从红花花瓣中克隆了查尔酮异构酶(CHI)和花青素合酶(ANS)的全长cDNA。 。

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