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首页> 外文期刊>Molecular ecology resources >Analysis of the black-chinned tilapia Sarotherodon melanotheron heudelotii reproducing under a wide range of salinities: From RNA-seq to candidate genes
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Analysis of the black-chinned tilapia Sarotherodon melanotheron heudelotii reproducing under a wide range of salinities: From RNA-seq to candidate genes

机译:在多种盐度下黑black罗非鱼Sarotherodon melanotheron heudelotii繁殖的分析:从RNA序列到候选基因

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The black-chinned tilapia Sarotherodon melanotheron heudelotii is an ecologically appealing model as it shows exceptional adaptive capacities, especially with regard to salinity. In spite of this, this species is devoid of genomic resources, which impedes the understanding of such remarkable features. De novo assembly of transcript sequences produced by next-generation sequencing technologies offers a rapid approach to obtain expressed gene sequences for non-model organisms. It also facilitates the development of quantitative real-time PCR (qPCR) assays for analysing gene expression under different environmental conditions. Nevertheless, obtaining accurate and reliable qPCR results from such data requires a number of validations prior to interpretation. The transcriptome of S. melanotheron was sequenced to discover transcripts potentially involved in the plasticity of male reproduction in response to salinity variations. A set of 54 candidate and reference genes was selected through a digital gene expression (DGE) approach, and a de novo qPCR assay using these genes was validated for further detailed expression analyses. A user-friendly web interface was created for easy handling of the sequence data. This sequence collection represents a major transcriptomic resource for S. melanotheron and will provide a useful tool for functional genomics and genetics studies.
机译:黑chin罗非鱼Sarotherodon melanotheron heudelotii是一种具有生态吸引力的模型,因为它具有出色的适应能力,特别是在盐度方面。尽管如此,该物种缺乏基因组资源,这妨碍了对这种显着特征的理解。从头组装由下一代测序技术产生的转录物序列提供了一种快速的方法来获得非模式生物的表达基因序列。它还促进了定量实时PCR(qPCR)分析方法的发展,用于分析不同环境条件下的基因表达。然而,从此类数据获得准确可靠的qPCR结果需要在解释之前进行大量验证。对S. melanotheron的转录组进行测序,以发现可能与盐度变化有关的雄性可塑性的转录本。通过数字基因表达(DGE)方法选择了一组54个候选基因和参考基因,并验证了使用这些基因进行的从头qPCR分析以进行进一步的详细表达分析。创建了一个用户友好的Web界面,可轻松处理序列数据。该序列集合代表了S. melanotheron的主要转录组资源,并将为功能基因组学和遗传学研究提供有用的工具。

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