Luo Weiwei, Zhou Ying, Wang Junru, Yu Xiaomu, Tong Jingou
State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, The Innovation Academy of Seed Design, Chinese Academy of Sciences, Wuhan, China.
College of Advanced Agricultural Sciences, University of Chinese Academy of Sciences, Beijing, China.
Front Genet. 2021 Jan 15;11:603454. doi: 10.3389/fgene.2020.603454. eCollection 2020.
Growth, one of the most important traits monitored in domestic animals, is essentially associated with bone development. To date, no large-scale transcriptome studies investigating bone development in bighead carp have been reported. In this study, we applied Isoform-sequencing technology to uncover the entire transcriptomic landscape of the bighead carp () in early growth stage, and obtained 63,873 non-redundant transcripts, 20,907 long non-coding RNAs, and 1,579 transcription factors. A total of 381 alternative splicing events were seen in the frontal and parietal bones with another 784 events simultaneously observed in the vertebral bones. Coupling this to RNA sequencing (RNA-seq) data, we identified 27 differentially expressed unigenes (DEGs) in the frontal and parietal bones and 45 DEGs in the vertebral bones in the fast-growing group of fish, when compared to the slow-growing group of fish. Finally, 15 key pathways and 20 key DEGs were identified and found to be involved in regulation of early growth such as energy metabolism, immune function, and cytoskeleton function and important cellular pathways such as the arginine and proline metabolic pathway (), FoxO signaling pathway (), cell adhesion molecules (, , and ), and peroxisome proliferator-activated receptor signaling pathway (). We established a novel full-length transcriptome resource and combined it with RNA-seq to elucidate the mechanism of genetic regulation of differential growth in bighead carp. The key DEGs identified in this study could fuel further studies investigating associations between growth and bone development and serve as a source of potential candidate genes for marker-assisted breeding programs.
生长是家畜中监测的最重要性状之一,本质上与骨骼发育相关。迄今为止,尚未有关于鳙鱼骨骼发育的大规模转录组研究报道。在本研究中,我们应用全长转录组测序技术揭示了鳙鱼早期生长阶段的整个转录组图谱,获得了63,873个非冗余转录本、20,907个长链非编码RNA和1,579个转录因子。在额骨和顶骨中总共观察到381个可变剪接事件,同时在椎骨中观察到另外784个事件。将此与RNA测序(RNA-seq)数据相结合,与生长缓慢的鱼群相比,我们在快速生长的鱼群的额骨和顶骨中鉴定出27个差异表达的单基因(DEG),在椎骨中鉴定出45个DEG。最后,鉴定出15条关键途径和20个关键DEG,发现它们参与早期生长的调节,如能量代谢、免疫功能和细胞骨架功能,以及重要的细胞途径,如精氨酸和脯氨酸代谢途径、FoxO信号通路、细胞粘附分子(、和)和过氧化物酶体增殖物激活受体信号通路。我们建立了一种新的全长转录组资源,并将其与RNA-seq相结合,以阐明鳙鱼差异生长的遗传调控机制。本研究中鉴定出的关键DEG可为进一步研究生长与骨骼发育之间的关联提供助力,并作为标记辅助育种计划潜在候选基因的来源。