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De novo metatranscriptome assembly and coral gene expression profile of Montipora capitata with growth anomaly

机译:具有生长异常的Montipora capitata的从头转录组装配和珊瑚基因表达谱

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Background Scleractinian corals are a vital component of coral reef ecosystems, and of significant cultural and economic value worldwide. As anthropogenic and natural stressors are contributing to a global decline of coral reefs, understanding coral health is critical to help preserve these ecosystems. Growth anomaly (GA) is a coral disease that has significant negative impacts on coral biology, yet our understanding of its etiology and pathology is lacking. In this study we used RNA-seq along with de novo metatranscriptome assembly and homology assignment to identify coral genes that are expressed in three distinct coral tissue types: tissue from healthy corals (“healthy”), GA lesion tissue from diseased corals (“GA-affected”) and apparently healthy tissue from diseased corals (“GA-unaffected”). We conducted pairwise comparisons of gene expression among these three tissue types to identify genes and pathways that help us to unravel the molecular pathology of this coral disease. Results The quality-filtered de novo-assembled metatranscriptome contained 76,063 genes, of which 13,643 were identified as putative coral genes. Overall gene expression profiles of coral genes revealed high similarity between healthy tissue samples, in contrast to high variance among diseased samples. This indicates GA has a variety of genetic effects at the colony level, including on seemingly healthy (GA-unaffected) tissue. A total of 105 unique coral genes were found differentially expressed among tissue types. Pairwise comparisons revealed the greatest number of differentially expressed genes between healthy and GA-affected tissue (93 genes), followed by healthy and GA-unaffected tissue (33 genes), and GA-affected and -unaffected tissue (7 genes). The putative function of these genes suggests GA is associated with changes in the activity of genes involved in developmental processes and activation of the immune system. Conclusion This is one of the first transcriptome-level studies to investigate coral GA, and the first metatranscriptome assembly for the M. capitata holobiont . The gene expression data, metatranscriptome assembly and methodology developed through this study represent a significant addition to the molecular information available to further our understanding of this coral disease.
机译:背景巩膜珊瑚是珊瑚礁生态系统的重要组成部分,在全世界具有重要的文化和经济价值。由于人为和自然压力正在促使全球珊瑚礁数量下降,因此了解珊瑚的健康状况对于保护这些生态系统至关重要。生长异常(GA)是一种珊瑚病,对珊瑚生物学具有重大的负面影响,但我们对其病因和病理学缺乏了解。在这项研究中,我们使用RNA-seq以及从头转录组装配和同源性分配来鉴定在三种不同的珊瑚组织类型中表达的珊瑚基因:健康珊瑚的组织(“健康”),患病珊瑚的GA病变组织(“ GA” -受影响的”和明显健康的组织(来自未患病的珊瑚)(“ GA-未受影响”)。我们对这三种组织类型之间的基因表达进行了成对比较,以鉴定有助于我们阐明该珊瑚病的分子病理学的基因和途径。结果从质量上进行了重新组装的元转录组包含76,063个基因,其中13,643个被鉴定为推定的珊瑚基因。珊瑚基因的总体基因表达谱显示,健康组织样品之间的相似性很高,而患病样品之间的差异却很大。这表明GA在菌落水平上具有多种遗传效应,包括在看似健康(未受GA影响)的组织上。共发现105种独特的珊瑚基因在不同组织类型中差异表达。配对比较显示,在健康和受GA影响的组织(93个基因)之间差异表达基因的数量最多,其次是健康和不受GA影响的组织(33个基因)以及受GA和不受影响的组织(7个基因)。这些基因的推定功能表明GA与参与发育过程和免疫系统活化的基因活性变化有关。结论这是最早研究珊瑚GA的转录组水平研究之一,也是首个M. capitata holobiont的转录组大会。通过这项研究开发的基因表达数据,元转录组汇编和方法学,为进一步加深我们对这种珊瑚病的了解提供了重要的分子信息。

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