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鸡ANP32家族蛋白亚细胞定位及其在免疫器官中的表达特征分析
引用本文:邢静如,石海英,王燕碧,赵采芹,唐宏,段志强. 鸡ANP32家族蛋白亚细胞定位及其在免疫器官中的表达特征分析[J]. 南方农业学报, 2022, 53(11): 3249-3256. DOI: 10.3969/j.issn.2095-1191.2022.11.026
作者姓名:邢静如  石海英  王燕碧  赵采芹  唐宏  段志强
作者单位:贵州大学动物科学学院/高原山地动物遗传育种与繁殖教育部重点实验室/贵州省动物遗传育种与繁殖重点实验室, 贵州贵阳 550025
基金项目:国家自然科学基金项目(31960698,31760732)贵州省地方家禽产业联合攻关项目(黔财农[2020]175号)贵州省科学技术基金项目(黔科合基础[2020]1Y134)
摘    要:【目的】明确鸡ANP32家族蛋白的亚细胞定位及在不同月龄鸡免疫器官中的表达特征,为后续研究鸡ANP32家族蛋白与新城疫病毒(NDV)复制及其致病性的关系打下基础。【方法】分别构建鸡ANP32家族基因重组真核表达载体,转染HEK-293T细胞后进行诱导表达,利用Western blotting检测融合蛋白表达情况,并通过荧光观察分析融合蛋白亚细胞定位;同时采用实时荧光定量PCR检测ANP32家族基因在1~6月龄鸡免疫器官(脾脏、胸腺和法氏囊)中的表达水平。【结果】成功构建了鸡ANP32家族基因重组真核表达载体pEGFP-C1-ANP32A、pEGFP-C1-ANP32B和pEGFP-C1-ANP32E,转染HEK-293T细胞后得到正确表达,获得携带EGFP标签的融合蛋白EGFP-ANP32A、EGFPANP32B和EGFP-ANP32E,其分子量分别为60.0、57.9和56.9 k D。亚细胞定位分析结果表明,融合蛋白EGFP-ANP32A、EGFP-ANP32B和EGFP-ANP32E的荧光与细胞核荧光完全重合,即主要定位在细胞核。实时荧光定量PCR检测结果表明,ANP32家族基因...

关 键 词:  ANP32家族蛋白  亚细胞定位  免疫器官  组织表达特征
收稿时间:2022-04-28

Subcellular localization of chicken ANP32 family members and their expression characteristics in chicken immune organs
XING Jing-ru,SHI Hai-ying,WANG Yan-bi,ZHAO Cai-qin,TANG Hong,DUAN Zhi-qiang. Subcellular localization of chicken ANP32 family members and their expression characteristics in chicken immune organs[J]. Journal of Southern Agriculture, 2022, 53(11): 3249-3256. DOI: 10.3969/j.issn.2095-1191.2022.11.026
Authors:XING Jing-ru  SHI Hai-ying  WANG Yan-bi  ZHAO Cai-qin  TANG Hong  DUAN Zhi-qiang
Affiliation:College of Animal Sciences, Guizhou University/Key Laboratory of Animal Genetics, Breeding and Reproduction in the Plateau Mountains Region, Ministry of Education/Key Laboratory of Animal Genetics, Breeding and Reproduction in Guizhou, Guiyang, Guizhou 550025, China
Abstract:【Objective】The aim of this study was to clarify the subcellular localization of chicken ANP32 family member proteins and their expression characteristics in immune organs of chicken at different months,which laid a foundation for the follow-up study of the relationship between chicken ANP32 family member proteins and Newcastle disease virus(NDV) replication and pathogenicity.【Method】The recombinant eukaryotic expression vectors of chicken ANP32 family member genes were constructed,induced their expression after transfection into HEK-293T cells.The expression and subcellular localization of the above fusion proteins was examined by Western blotting and fluorescence observation,respectively. At the same time,the expression levels of chicken ANP32 family member genes in immune organs(spleen,thymus and bursa of Fabricius) at 1-to 6-month-old chicken was detected by real-time fluorescence quantitative PCR(RT-qPCR).【Result】The recombinant eukaryotic expression vectors(including pEGFP-C1-ANP32A,pEGFP-C1-ANP32B and pEGFP-C1-ANP32E) of chicken ANP32 family member genes were successfully constructed and the fusion proteins with EGFP tags EGFP-ANP32A,EGFP-ANP32B and EGFP-ANP32E were obtained after transfection into HEK-293T cells.Their molecular weights were 60.0,57.9 and 56.9 kD respectively. The results of subcellular localization analysis showed that the fluorescence of fusion proteins EGFP-ANP32A,EGFP-ANP32B and EGFP-ANP32E completely coincided with the nuclear fluorescence,that was,they were mainly located in the nucleus. The results of RT-qPCR assay showed that ANP32 family member genes were expressed in immune organs(spleen,thymus and bursa of Fabricius) of 1-to 6-monthold chicken,and the expression level of ANP32 family member genes was different in different immune organs. The expression of ANP32A and ANP32E genes in the immune organs of 1-to 6-month-old chicken increased first and then decreased,which reached the peak in the immune organs of 2-month-old chicken. The expression of ANP32B gene showed a downward trend,with the highest relative expression in the immune organs of 1-month-old chicken.【Conclusion】Chicken ANP32 family member proteins are mainly located in the nucleus,and ANP32 family member genes are expressed in the immune organs at different months,but the three genes have their own unique expression characteristics. Therefore,the relationship between different expression levels and the development of immune organs and immune function deserved to be further explored.
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