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UBE2G1 是大黄鱼()感染免疫反应的关键组成部分。

UBE2G1 Is a Critical Component of Immune Response to the Infection of in Large Yellow Croaker ().

机构信息

Key Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture and Rural Affairs, Fujian Provincial Key Laboratory of Marine Fishery Resources and Eco-Environment, Fisheries College, Jimei University, Xiamen 361021, China.

Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, China.

出版信息

Int J Mol Sci. 2022 Jul 27;23(15):8298. doi: 10.3390/ijms23158298.

DOI:10.3390/ijms23158298
PMID:35955424
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9368838/
Abstract

The large yellow croaker () is one of the most economically valuable mariculture fish in China. Infection of can cause an outbreak of "internal organ white-spot disease", which seriously affects the aquaculture of the large yellow croaker. Ubiquitylation is closely related to the post-translation modification of proteins and plays a vital role in many hosts' immune defense pathways, while the E2-binding enzyme is a key factor in ubiquitination. Our previous genome-wide association study found that the ubiquitin-binding enzyme E2G1 (designed ) was one of the candidate genes related to disease resistance in large yellow croaker. In this study, we analyzed the molecular characteristics, function, and immune mechanism of the . The full-length cDNA is 812 bp, with an open reading frame of 513 bp, encoding 170 amino acid residues. The results of the RT-qPCR and immunohistochemistry analysis revealed that its transcription and translation were significantly activated by the infection of in large yellow croaker. Immunocytochemistry experiments verified the co-localization of UBE2G1 and the ubiquitin proteins in the head kidney cells of large yellow croaker. Through GST pull-down, we found that UBE2G1 interacted with NEDD8 to co-regulate the ubiquitination process. The above results indicate that UBE2G1 is essential in the regulation of ubiquitination against infection in large yellow croaker, which lays a foundation for further study on the resistance mechanism of internal organ white-spot disease.

摘要

大黄鱼()是中国最具经济价值的海水养殖鱼类之一。感染()可引起“内脏白点病”的爆发,严重影响大黄鱼的养殖业。泛素化与蛋白质的翻译后修饰密切相关,在许多宿主的免疫防御途径中发挥着重要作用,而 E2 结合酶是泛素化的关键因素。我们之前的全基因组关联研究发现,泛素结合酶 E2G1(设计为)是与大黄鱼抗病性相关的候选基因之一。在这项研究中,我们分析了 的分子特征、功能和免疫机制。其全长 cDNA 为 812bp,开放阅读框为 513bp,编码 170 个氨基酸残基。RT-qPCR 和免疫组织化学分析的结果表明,在大黄鱼感染后,其转录和翻译明显被激活。免疫细胞化学实验验证了 UBE2G1 和泛素蛋白在大黄鱼头肾细胞中的共定位。通过 GST 下拉实验,我们发现 UBE2G1 与 NEDD8 相互作用,共同调节泛素化过程。上述结果表明,UBE2G1 在大黄鱼抵御感染的泛素化调节中至关重要,为进一步研究内脏白点病的抗病机制奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7e0/9368838/4ef9dc63e706/ijms-23-08298-g007.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7e0/9368838/4ef9dc63e706/ijms-23-08298-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7e0/9368838/c04dc42f25ff/ijms-23-08298-g002.jpg
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