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Differential mantle transcriptomics and characterization of growth-related genes in the diploid and triploid pearl oyster Pinctada fucata

机译:二倍体和三倍体珍珠牡蛎Pinctada Fucata的差异披风转录组织和生长相关基因的特征

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To explore the molecular mechanism of triploidy effect in the pearl oyster Pinctada fucata, two RNA-seq libraries were constructed from the mantle tissue of diploids and triploids by Roche-454 massive parallel pyrosequencing. The identification of differential expressed genes (DEGs) between diploid and triploid may reveal the molecular mechanism of triploidy effect. In this study, 230 down-regulated and 259 up-regulated DEGs were obtained by comparison between diploid and triploid libraries. The gene ontology and KEGG pathway analysis revealed more functional activation in triploids and it may due to the duplicated gene expression in transcriptional level during whole genome duplication (WGD). To confirm the sequencing data, a set of 11 up-regulated genes related to growth and development control and regulation were analyzed by RT-qPCR in independent experiment. According to the validation and annotation of these genes, it is hypothesized that the set of up-regulated expressed genes had the correlated expression pattern involved in shell building or other interactive probable functions during triploidization. The up- regulation of growth-related genes may support the classic hypotheses of 'energy redistribution' from early research. The results provide valuable resources to understand the molecular mechanism of triploidy effect in both shell building and producing high-quality seawater pearls. (C) 2017 Elsevier B.V. All rights reserved.
机译:为了探讨珍珠牡蛎Pinctada Fucata中三倍体效应的分子机制,通过罗氏-454大规模平行焦酶测序从二倍体和三倍体的地幔组织构建了两种RNA-SEQ文库。二倍体和三倍体之间的差异表达基因(DEGS)的鉴定可能揭示三重效应的分子机制。在本研究中,通过二倍体和三倍体文库进行比较获得230个下调和259个上调的次数。基因本体论和Kegg途径分析显示了三倍体中的更功能活化,并且由于全基因组重复(WGD)中转录水平的重复表达是由于转录水平的重复表达。为了确认测序数据,通过RT-QPCR在独立实验中分析了一组与生长和显影和调节相关的11个上调基因。根据这些基因的验证和注释,假设该组上调表达基因具有在三倍化期间涉及壳体建筑物或其他交互可能的功能的相关表达模式。生长相关基因的调节可能支持早期研究的“能源再分配”的经典假设。结果提供了有价值的资源,以了解壳牌建设和生产高品质海水珍珠的三倍体效应的分子机制。 (c)2017 Elsevier B.v.保留所有权利。

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