首页> 外文期刊>Hydrobiologia >Cloning of proliferating cell nuclear antigen gene from the dinoflagellate Prorocentrum donghaiense and monitoring its expression profiles by real-time RT-PCR.
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Cloning of proliferating cell nuclear antigen gene from the dinoflagellate Prorocentrum donghaiense and monitoring its expression profiles by real-time RT-PCR.

机译:克隆鞭毛原核生物中的增殖细胞核抗原基因,并通过实时RT-PCR监测其表达谱。

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摘要

The growth rate of marine phytoplankton at the species level is an important parameter for estimating a phytoplankton population in the field. Therefore, monitoring this rate may have potential to be useful for providing early warnings for red tide blooms. We investigated the proliferating cell nuclear antigen (PCNA) gene of the red tide species Prorocentrum donghaiense Lu et Goebel to study the relationship between its expression level and the growth rate. The gene was isolated and the full cDNA sequence encoding PCNA was obtained. It consisted of 1,057 base pairs (bp), comprising 81 bp of the 5' untranslated region (UTR) and 196 bp of the 3' UTR, and had an open reading frame (ORF) of 780 bp, encoding 259 amino acid residues. The coding region was highly conserved compared with other organisms PCNA gene. Using real-time PCR, we found that the average of PCNA transcript, normalized to per cell basis, decreased obviously from 26.12+or-3.04 copies in the exponential and transition phase to 5.95+or-0.79 copies in the stationary phase. However, in the decline phase, the copies of PCNA transcription per cell is below one copy. Furthermore, the expression level of PCNA changed consistently with the growth rate as assessed by the relative quantitation method. These results indicate that PCNA has a potential as a molecular marker of growth phase and rate for P. donghaiense. This may help in forecasting blooms, allowing for effective control measures to be implemented in a timely fashion.
机译:海洋浮游植物在物种水平上的增长率是估算田间浮游植物种群数量的重要参数。因此,监视此速率可能对提供红潮水华早期预警很有用。我们研究了赤潮物种东海原藻> Lu et Goebel的增殖细胞核抗原(PCNA)基因,以研究其表达水平与生长速率之间的关系。分离基因,获得编码PCNA的完整cDNA序列。它由1,057个碱基对(bp)组成,包括81 bp的5'非翻译区(UTR)和196 bp的3'UTR,并具有780 bp的开放阅读框(ORF),编码259个氨基酸残基。与其他生物PCNA基因相比,编码区高度保守。使用实时PCR,我们发现按细胞标准化的PCNA转录本的平均值从指数期和过渡期的26.12 +或-3.04份下降到固定期的5.95 +或-0.79份。但是,在下降阶段,每个细胞PCNA转录的拷贝数低于一个拷贝。此外,通过相对定量方法评估,PCNA的表达水平与生长速率一致。这些结果表明,PCNA具有作为生长相和iP速率的分子标志物的潜力。 donghaiense 。这可能有助于预测水华,从而及时采取有效的控制措施。

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