Comparative analysis of salmonid non-classical MHC class I U lineage genes: Promoter architecture and transcriptional responses with a focus on Atlantic salmon

IF 2.4 3区 农林科学 Q1 FISHERIES
Developmental and comparative immunology Pub Date : 2026-07-01 Epub Date: 2026-06-11 DOI:10.1016/j.dci.2026.105650
Atefeh Kianian, Maryam Imam, Agata T. Gondek-Wyrozemska, Linn Greiner-Tollersrud, Eva-Stina Edholm
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引用次数: 0

Abstract

In addition to highly polymorphic classical MHC class I genes, teleost fish also possess variable numbers of non-classical MHC class I genes, the functions of which are largely unknown. This work focuses on genes belonging to the non-classical MHC class I U lineage revealing unique evolutionary and regulatory patterns across salmonids, indicative of sub-clade specific and diversified functional roles. Comparative analysis of a total of 175 salmonid U lineage genes supported a classification into seven subclades following one of two main evolutionary patterns indicative of different selective pressures. Genes belonging to the ULA, UC/DA, UFA, and UZA sub-clades exhibited variable degrees of species-specific diversification, characterized by gene duplications, gene loss and pseudogenization. In contrast, the UGA, UEA, and UHA sub-clades have remained conserved, with minimal sequence divergence across divergent species, suggesting functional constraints. Notably, the UGA subclade represents a striking example of conservation across divergent salmonid species. Promoter analyses of the U lineage subclades revealed two main regulatory architectures: i) overall conserved promoter elements similar to the UBA gene in ULA, UFA, and UZA, implying shared transcriptional regulation; and ii) divergent promoters in UGA, UEA, UC/DA and UHA suggesting diversified regulatory mechanisms. Expression profiling further supported functional diversity, revealing non-classical U lineage subclade specific expression patterns and variable expression levels. While non-classical U lineage genes, as a group, showed limited response to stimulation with viral mimics, subclade specific responses were observed following infection with salmon alpha virus 3 (SAV3) and in response to interferon stimulation. Similar to the classical UBA gene, UGA and, to a lesser extent, UHA transcript expression levels were upregulated in response to stimulation with either type I IFNa1 or type II IFNγ, as well as in response to SAV3 infection but not to IFNc stimulation. In contrast, UC/DA and UEA genes showed minimal response to interferon stimulation or SAV3 challenge. Combined, these findings underscore the adaptability and complexity of the salmonid MHC class I system and provide a comprehensive framework for understanding the diversification of salmonid MHC class I genes, offering valuable insights into the variation, regulation, and potential roles of these genes in salmonid immunity.
鲑鱼非经典MHC I类U谱系基因的比较分析:启动子结构和转录反应——以大西洋鲑鱼为中心。
除了高度多态性的经典MHC I类基因外,硬骨鱼还具有可变数量的非经典MHC I类基因,其功能在很大程度上是未知的。这项工作的重点是属于非经典MHC I类U谱系的基因,揭示了鲑科鱼类独特的进化和调节模式,表明亚分支特异性和多样化的功能作用。对175个鲑鱼U系基因的比较分析支持将其分为7个亚支系,这些亚支系遵循两种主要进化模式中的一种,表明了不同的选择压力。ULA、UC/DA、UFA和UZA亚枝的基因表现出不同程度的物种特异性多样化,表现为基因重复、基因丢失和假原化。相比之下,UGA、UEA和UHA亚枝仍然保持保守,不同物种之间的序列差异最小,表明功能限制。值得注意的是,UGA亚分支代表了不同鲑鱼物种保护的一个显著例子。对U谱系亚支的启动子分析揭示了两种主要的调控结构:1)在ULA、UFA和UZA中,启动子元件总体上与UBA基因相似,这意味着共享转录调控;UGA、UEA、UC/DA和UHA的启动子存在差异,表明调控机制存在差异。表达谱进一步支持了功能多样性,揭示了非经典U谱系亚枝特异性表达模式和可变表达水平。虽然非经典U谱系基因作为一个群体,对病毒模拟物的刺激反应有限,但在感染鲑鱼α病毒3 (SAV3)和对干扰素刺激的反应中,观察到亚分支特异性反应。与经典的UBA基因类似,UGA和UHA转录物的表达水平在较小程度上受到I型IFNa1或II型IFNγ的刺激,以及SAV3感染的反应,但不受IFNc刺激的影响。相比之下,UC/DA和UEA基因对干扰素刺激或SAV3攻击的反应最小。综上所述,这些发现强调了鲑鱼MHC I类系统的适应性和复杂性,并为理解鲑鱼MHC I类基因的多样性提供了一个全面的框架,为这些基因在鲑鱼免疫中的变异、调控和潜在作用提供了有价值的见解。
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来源期刊
CiteScore
6.20
自引率
6.90%
发文量
206
审稿时长
49 days
期刊介绍: Developmental and Comparative Immunology (DCI) is an international journal that publishes articles describing original research in all areas of immunology, including comparative aspects of immunity and the evolution and development of the immune system. Manuscripts describing studies of immune systems in both vertebrates and invertebrates are welcome. All levels of immunological investigations are appropriate: organismal, cellular, biochemical and molecular genetics, extending to such fields as aging of the immune system, interaction between the immune and neuroendocrine system and intestinal immunity.
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