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失而复得:鲑鱼类 NF-κB 抑制剂家族比想象的更大。

Lost and Found: The Family of NF-κB Inhibitors Is Larger than Assumed in Salmonid Fish.

机构信息

Institute of Genome Biology, Research Institute for Farm Animal Biology (FBN), 18196 Dummerstorf, Germany.

VIM, UVSQ, INRAE, Université Paris-Saclay, 78350 Jouy-en-Josas, France.

出版信息

Int J Mol Sci. 2023 Jun 16;24(12):10229. doi: 10.3390/ijms241210229.

DOI:10.3390/ijms241210229
PMID:37373375
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10299181/
Abstract

NF-κB signalling is largely controlled by the family of 'inhibitors of NF-κB' (IκB). The relevant databases indicate that the genome of rainbow trout contains multiple gene copies coding for iκbα (), iκbε (), iκbδ (), iκbζ (), and , but it lacks iκbβ () and iκbη (). Strikingly, three paralogs are apparently present in salmonid fish, two of which share a high sequence identity, while the third putative gene is significantly less like its two paralogs. This particular gene product, iκbα, clusters with the human IκBβ in a phylogenetic analysis, while the other two iκbα proteins from trout associate with their human IκBα counterpart. The transcript concentrations were significantly higher for the structurally more closely related paralogs than for the structurally less similar paralog, suggesting that iκbβ probably has not been lost from the salmonid genomes but has been incorrectly designated as iκbα. In the present study, two gene variants coding for iκbα () and iκbε () were prominently expressed in the immune tissues and, particularly, in a cell fraction enriched with granulocytes, monocytes/macrophages, and dendritic cells from the head kidney of rainbow trout. Stimulation of salmonid CHSE-214 cells with zymosan significantly upregulated the iκbα-encoding gene while elevating the copy numbers of the inflammatory markers interleukin-1-beta and interleukin-8. Overexpression of iκbα and iκbε in CHSE-214 cells dose-dependently quenched both the basal and stimulated activity of an NF-κB promoter suggesting their involvement in immune-regulatory processes. This study provides the first functional data on iκbε-versus the well-researched iκbα factor-in a non-mammalian model species.

摘要

NF-κB 信号主要受“NF-κB 抑制剂”(IκB)家族控制。相关数据库表明,虹鳟基因组包含多个编码 Iκbα()、Iκbε()、Iκbδ()、Iκbζ()和的基因拷贝,但缺乏 Iκbβ()和 Iκbη()。引人注目的是,三个似乎存在于鲑鱼目中的基因,其中两个具有高度的序列同一性,而第三个假定的基因与它的两个基因明显不同。这种特殊的基因产物 Iκbα在系统发育分析中与人类 IκBβ聚类,而来自鳟鱼的另外两种 Iκbα 蛋白与它们的人类 IκBα 对应物相关联。与结构上不太相似的基因相比,结构上更接近的基因的转录浓度明显更高,这表明 Iκbβ 可能没有从鲑鱼基因组中丢失,而是被错误地指定为 Iκbα。在本研究中,编码 Iκbα()和 Iκbε()的两个基因变体在免疫组织中显著表达,特别是在富含头肾粒细胞、单核细胞/巨噬细胞和树突状细胞的细胞部分中。用酵母聚糖刺激鲑鱼 CHSE-214 细胞显著上调编码 Iκbα 的基因,同时提高炎症标志物白细胞介素-1-β和白细胞介素-8 的拷贝数。在 CHSE-214 细胞中过表达 Iκbα 和 Iκbε 剂量依赖性地抑制 NF-κB 启动子的基础和刺激活性,表明它们参与免疫调节过程。这项研究提供了在非哺乳动物模型物种中 Iκbε 与研究充分的 Iκbα 因子的第一个功能数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/9164c8510443/ijms-24-10229-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/dda85bb0d199/ijms-24-10229-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/fa8639745900/ijms-24-10229-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/85468980dc8f/ijms-24-10229-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/7d0f9947c231/ijms-24-10229-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/9b60aed2b70f/ijms-24-10229-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/eebc206251c3/ijms-24-10229-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/442c75727173/ijms-24-10229-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/3cbcf4576f06/ijms-24-10229-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/9164c8510443/ijms-24-10229-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/dda85bb0d199/ijms-24-10229-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/fa8639745900/ijms-24-10229-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/85468980dc8f/ijms-24-10229-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/7d0f9947c231/ijms-24-10229-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/9b60aed2b70f/ijms-24-10229-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/eebc206251c3/ijms-24-10229-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/442c75727173/ijms-24-10229-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/3cbcf4576f06/ijms-24-10229-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1563/10299181/9164c8510443/ijms-24-10229-g009.jpg

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