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Diversity of Phytoplankton Nitrate Transporter Sequences from Isolated Single Cells and Mixed Samples from the East China Sea and mRNA Quantification

机译:东海分离的单细胞和混合样本中浮游植物硝酸盐转运蛋白序列的多样性和mRNA定量

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The transcript abundances of nitrate transporter genes ( Nrt2 ) were proposed as potential markers for nitrogen deficiency in marine diatoms. To correctly quantify diatom Nrt2 mRNA in the East China Sea (ECS), we utilized both mixed-species sequencing and single-cell PCR to expand the sequence database for this region. Using the single-cell method of PCR, 9 new diatom Nrt2 sequences belonging to 5 genera, the Nrt2 sequences of which have never been reported before, were obtained. On the other hand, 291 sequences homologous to Nrt2 were retrieved from mixed-species sequencing using degenerate primers, and these sequences were clustered into 12 major groups according to a phylogenetic analysis. Based on sequence alignments, 11 pairs of group-specific PCR primers were designed to detect Nrt2 mRNA levels in the ECS, and 3 of these primer pairs showed high specificity to target species. In ECS phytoplankton samples, environmental RNA was amplified via antisense RNA amplification followed by cDNA production. Subsequently, Nrt2 transcript levels were readily detected using quantitative PCR. Our results indicated that investigating sequence diversity followed by careful primer design and evaluation is a good strategy to quantify the expression of genes of ecologically important phytoplankton.
机译:提出了硝酸盐转运蛋白基因(Nrt2)的转录本丰度作为海洋硅藻氮缺乏的潜在标志。为了正确定量东海(ECS)中的硅藻Nrt2 mRNA,我们利用混合物种测序和单细胞PCR来扩展该区域的序列数据库。使用单细胞PCR方法,获得了属于5属的9个新的硅藻Nrt2序列,其以前从未报道过。另一方面,使用简并引物从混合物种测序中检索到与Nrt2同源的291个序列,并根据系统发育分析将这些序列分为12个主要组。基于序列比对,设计了11对组特异性PCR引物来检测ECS中的Nrt2 mRNA水平,其中3对引物显示出对靶标物种的高度特异性。在ECS浮游植物样品中,通过反义RNA扩增随后生成cDNA扩增环境RNA。随后,使用定量PCR可轻松检测Nrt2转录水平。我们的结果表明,研究序列多样性,然后仔细进行引物设计和评估,是量化具有重要生态意义的浮游植物基因表达的良好策略。

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