Key Laboratory of Mariculture & Stock Enhancement in the North China Sea, Ministry of Agriculture, Dalian Ocean University, Dalian, 116023, China.
College of Fisheries and Life Science, Dalian Ocean University, 52 Heishijiao Street, Shahekou District, Dalian, 116023, China.
Mar Biotechnol (NY). 2018 Apr;20(2):193-205. doi: 10.1007/s10126-018-9796-6. Epub 2018 Feb 28.
Heterosis is important for sea cucumber breeding, but its molecular mechanism remains largely unexplored. In this study, parental lines of Apostichopus japonicus from Russia (R) and China (C) were used to construct hybrids (CR and RC) by reciprocal crossing. We examined the transcriptional profiles of the hybrids (CR and RC) and the purebreds (CC and RR) at different developmental times. A total of 60.27 Gb of clean data was obtained, and 176,649 unigenes were identified, of which 50,312 unigenes were annotated. A total of 414,536 SNPs were identified. A total of 7011 differentially expressed genes (DEGs) were obtained between the purebreds and hybrids at 45 days after fertilization (DAF), and a total of 8218 DEGs were obtained between the purebreds and hybrids at 75 DAF. In addition, a total of 7652 DEGs were obtained between 45 DAF and 75 DAF. The significant DEGs were mainly involved in the MAPK and FOXO signaling pathways, especially in the Ras-Raf-MEK1/2-ERK module, which may be a key regulator of development and growth in juvenile A. japonicus. In addition, we also identified key growth-related genes, such as fgfs, igfs, megfs and hgfs, which were upregulated in the hybrids (RC and CR); these genes may play important roles in heterosis in A. japonicus. Our study provides fundamental information on the molecular mechanisms underlying heterosis in sea cucumber and might suggest strategies for the selection of rapidly growing strains of sea cucumber in aquaculture.
杂种优势在海参养殖中很重要,但它的分子机制在很大程度上仍未被探索。在这项研究中,我们使用来自俄罗斯(R)和中国(C)的刺参亲本构建了杂交种(CR 和 RC),并通过回交获得了它们的纯系(CC 和 RR)。我们在不同的发育时间检查了杂种(CR 和 RC)和纯系(CC 和 RR)的转录谱。共获得了 60.27 Gb 的清洁数据,并鉴定了 176649 个非编码 RNA 基因,其中 50312 个非编码 RNA 基因被注释。共鉴定出 414536 个单核苷酸多态性(SNP)。在受精后 45 天(DAF),纯系和杂种之间共获得了 7011 个差异表达基因(DEG),在 75 DAF 时共获得了 8218 个 DEG。此外,在 45 DAF 和 75 DAF 之间共获得了 7652 个 DEG。显著的差异表达基因主要涉及 MAPK 和 FOXO 信号通路,特别是 Ras-Raf-MEK1/2-ERK 模块,这可能是幼参生长发育的关键调节剂。此外,我们还鉴定了关键的生长相关基因,如 fgfs、igfs、megfs 和 hgfs,它们在杂种(RC 和 CR)中上调;这些基因可能在刺参杂种优势中发挥重要作用。我们的研究为海参杂种优势的分子机制提供了基础信息,并可能为水产养殖中选择快速生长的海参品种提供策略。