机构地区:[1]河南农业大学动物科技学院,郑州450046 [2]华兰生物工程股份有限公司,新乡453003
出 处:《中国畜牧兽医》2023年第10期3882-3895,共14页China Animal Husbandry & Veterinary Medicine
基 金:国家自然科学基金项目(31702359);河南省科技研发计划联合基金(202217);河南省高等学校重点科研项目(23A240001)。
摘 要:【目的】试验旨在克隆鲤(Cyprinus carpio)环指蛋白145(ring finger protein145,RNF145)基因CDS区,并对其进行生物信息学分析及功能初探。【方法】对鲤RNF 145基因进行了克隆并测序,通过在线软件对鲤RNF145蛋白进行生物信息学分析;采用实时荧光定量PCR分析鲤RNF 145基因在不同发育阶段、不同组织中及在鲤春病毒血症病毒(Spring Viremia of Carp virus,SVCV)和Poly(I∶C)刺激下的mRNA表达变化。【结果】鲤RNF 145基因CDS序列全长2049 bp,编码682个氨基酸,其氨基酸序列与鲫相似性最高;鲤RNF145蛋白分子质量为76.56 ku,理论等电点为6.16,脂肪系数为115.32%,不稳定指数为41.87,无信号肽,含有11个跨膜螺旋,属跨膜蛋白;亚细胞定位预测结果显示,其定位于细胞质膜(87%)和内质网(13%);该蛋白含有TRC8-N、RING_H2_RNF145和RAD18结构域,具有α-螺旋(56.45%)、延伸链(9.68%)、β-转角(2.35%)及无规则卷曲(31.52%),与MFN2、NUGGC.1、ASZ1和TRIM36相互作用的置信度较高。早期发育阶段鲤RNF 145基因mRNA表达呈先显著下降后上升,再显著下降趋势(P<0.05);组织表达谱分析表明,其在脾脏中表达量最高,在肝脏中表达量最低;SVCV1(5.6×107 TCID 50/mL)在体感染24 h后,RNF 145基因在肌肉、脾脏、头肾、心脏中表达量均显著升高,在肝脏中则显著下降(P<0.05);该剂量感染鲤上皮瘤细胞(Epithelioma papulosum crprini,EPC)时,RNF 145基因表达量在12 h时开始显著升高,于48 h时仍显著高于对照组(P<0.05);SVCV2(5.6×104 TCID 50/mL)感染EPC时,鲤RNF 145基因mRNA表达量在感染后24 h时显著高于对照组,48 h后显著低于对照组(P<0.05)。与SVCV1刺激结果不同,在体注射Poly(I∶C)(1000μg/mL)24 h后,该基因在脾脏和头肾中表达量均显著低于对照组(P<0.05);Poly(I∶C)(10μg/mL)感染EPC时,鲤RNF 145基因mRNA表达量在感染后24 h时显著高于对照组,48 h后显著低于对照组(P<0.05)。【结论】本试验成功克隆了鲤RNF 145基因�【Objective】The purpose of this study was to clone the CDS region of ring finger protein 145(RNF145)gene in Cyprinus carpio,and conduct bioinformatics analysis and functional investigation on it.【Method】RNF 145 gene in Cyprinus carpio was cloned and sequenced,and bioinformatics analysis of RNF145 protein in Cyprinus carpio was performed using online softwares.The mRNA expression changes of RNF 145 gene of Cyprinus carpio in different development stages,different tissues and stimulated by Spring Viremia of Carp virus(SVCV)and Poly(I∶C)were analyzed by Real-time quantitative PCR.【Result】The full-length CDS sequence of RNF 145 gene in Cyprinus carpio was 2049 bp,encoding 682 amino acids.Its amino acid sequence had the highest similarity to that of Carassius auratus.The molecular weight of RNF145 protein in Cyprinus carpio was 76.56 ku,the theoretical isoelectric point was 6.16,the fat index was 115.32%,the instability index was 41.87,there was no signal peptide,and it contained 11 transmembrane helices,belonging to transmembrane protein.The results of subcellular localization prediction showed that it was located in the plasma membrane(87%)and endoplasmic reticulum(13%).This protein contained TRC8-N domain,RING_H2_RNF145 domain and RAD18 domain,and had typical RING-finger family characteristics,with alpha helix(56.45%),extended chain(9.68%),beta turn(2.35%)and random coil(31.52%).The confidence level for interactions with MFN2,NUGGC.1,ASZ1,and TRIM36 were high.In the early developmental stage,the mRNA expression of RNF 145 gene in Cyprinus carpio showed a significant decrease followed by an increase,followed by a significant decrease(P<0.05).The analysis of tissue expression profile showed that its expression was the highest in spleen and the lowest in liver.After 24 h of in vivo infection with SVCV1(5.6×107 TCID 50/mL),the expression of RNF 145 gene was significantly increased in muscle,spleen,head kidney and heart tissues,but significantly decreased in liver(P<0.05).When infecting carp epithelial tum
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