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基于 iTRAQ 的定量蛋白质组学分析为深入了解番鸭(Cairina moschata)伴发强烈就巢性提供了新视角,并结合代谢组学分析。

iTRAQ-based quantitative proteomic analysis provides insights into strong broodiness in Muscovy duck (Cairina moschata) combined with metabolomics analysis.

机构信息

Institutional addresses: College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou 350002, Fujian, PR China.

Institutional addresses: College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou 350002, Fujian, PR China..

出版信息

J Proteomics. 2019 Jul 30;204:103401. doi: 10.1016/j.jprot.2019.103401. Epub 2019 May 30.

Abstract

Much attention has been paid to the broodiness of the Muscovy duck, but the molecular mechanism of broodiness remains largely unknown. In this study, the ovary tissues of Muscovy ducks during the broody and laying periods were used to investigate differentially expressed proteins (DEPs) by the iTRAQ-based proteomics approach. A total of 335 DEPs were identified, including 139 up-regulated and 196 down-regulated proteins. Six proteins (APOV1, GAL, SAA, GNB5, VLDLR and CDK1) with higher changes in expression were selected, and these proteins are mainly involved in the pathways related to reproductive performance, such as Oocyte meiosis, and PI3K-Akt signaling pathway. Steroid biosynthesis was the most significantly enriched pathway by KEGG pathway enriched analysis. The qRT-PCR analysis was applied to verify the proteomic analysis. Meanwhile, metabolomics analysis found that several important differentially expressed metabolites (DEMs) (7-dehydrodesmosterol, 25-Hydroxyvitamin D3, 7-Dehydrocholesterol, Pregnanolone, Allopregnanolone and estrogen) that were also mainly involved in Steroid biosynthesis, Steroid hormone biosynthesis and Metabolic pathways. Crucially, the changes in the abundance of these metabolites are closely related to the changes in the protein abundance of proteins identified in the same pathway, and it is always the upstream key enzymes that influence the production of downstream metabolites.

摘要

人们对麝香鸭的抱窝性给予了极大关注,但抱窝性的分子机制在很大程度上仍不清楚。在这项研究中,采用 iTRAQ 基于蛋白质组学方法研究了抱窝期和产蛋期麝香鸭的卵巢组织中的差异表达蛋白(DEPs)。共鉴定出 335 个 DEPs,包括 139 个上调蛋白和 196 个下调蛋白。选择了 6 个表达变化较大的蛋白质(APOV1、GAL、SAA、GNB5、VLDLR 和 CDK1),这些蛋白质主要涉及生殖性能相关途径,如卵母细胞减数分裂和 PI3K-Akt 信号通路。类固醇生物合成是通过 KEGG 途径富集分析得到的最显著富集途径。qRT-PCR 分析用于验证蛋白质组学分析。同时,代谢组学分析发现了一些重要的差异表达代谢物(DEMs)(7-脱氢胆甾醇、25-羟基维生素 D3、7-脱氢胆固醇、孕烷醇酮、别孕烷醇酮和雌激素),这些代谢物也主要参与类固醇生物合成、类固醇激素生物合成和代谢途径。至关重要的是,这些代谢物丰度的变化与同一途径中鉴定的蛋白质丰度变化密切相关,并且总是上游关键酶影响下游代谢物的产生。

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