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比较转录组、数字基因表达和蛋白质组分析为[具体物种]从大眼幼体到第一期幼体的短尾化过程提供了见解。

Comparative transcriptome, digital gene expression and proteome profiling analyses provide insights into the brachyurization from the megalopa to the first juvenile in .

作者信息

Yang Yunxia, Jin Fangcao, Liu Wanyi, Huo Guangming, Zhou Feng, Yan Jie, Zhou Kaiya, Li Peng

机构信息

School of Fishery, Zhejiang Ocean University, Zhoushan 316022, PR China.

Jiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing 210023, PR China.

出版信息

Heliyon. 2023 Jan 7;9(1):e12736. doi: 10.1016/j.heliyon.2022.e12736. eCollection 2023 Jan.

Abstract

larva normally experiences 11 stages. The reduced abdomen folded beneath the thorax is the most prominent characteristic of morphological alteration from megalopa to juvenile crab. Up to date, the molecular mechanisms of brachyurization remain a mystery. Here, transcriptome library, digital gene expression (DGE) libraries and proteome libraries at two developmental stages [the megalopa stage of (stage M) and the first stage of juvenile crab (stage J1)] of the Chinese mitten crab larva were constructed for RNA sequencing and iTRAQ approaches followed by bioinformatics analysis, respectively. In total, 1106 genes and 871 proteins were differentially expressed between the stage M and stage J1. Moreover, several important pathways were identified, including biosynthesis of secondary metabolites, metabolic pathways, focal adhesion, and some disease pathways. Besides, muscle contraction, oxidative phosphorylation, calcium signaling, PI3K-Akt, DNA replication pathway, and integrin signaling pathway also had important functions in brachyurization process. Furthermore, the components, actin, actin-related protein, collagens, filamin-A/B, laminin, integrins, paxillin, and fibronectin had up-regulated expression levels in M stage compared to J1 stage.

摘要

幼体通常经历11个阶段。折叠于胸部下方的缩小腹部是从大眼幼体到幼蟹形态改变的最显著特征。迄今为止,短尾化的分子机制仍是个谜。在此,构建了中华绒螯蟹幼体两个发育阶段[大眼幼体阶段(M期)和幼蟹第一阶段(J1期)]的转录组文库、数字基因表达(DGE)文库和蛋白质组文库,分别用于RNA测序和iTRAQ方法,随后进行生物信息学分析。在M期和J1期之间总共鉴定出1106个差异表达基因和871种差异表达蛋白质。此外,还确定了几个重要途径,包括次生代谢物的生物合成、代谢途径、粘着斑以及一些疾病途径。此外,肌肉收缩、氧化磷酸化、钙信号传导、PI3K-Akt、DNA复制途径和整合素信号传导途径在短尾化过程中也具有重要作用。此外,与J1期相比,肌动蛋白、肌动蛋白相关蛋白、胶原蛋白、细丝蛋白-A/B、层粘连蛋白、整合素、桩蛋白和纤连蛋白等成分在M期表达水平上调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d349/9853305/c8cf81a319a3/gr1.jpg

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