Wang J, Liu Y, Dong W H, Huo Y J, Huang X G, Wu S L, Bao W B
College of Animal Science and Technology, Key Laboratory for Animal Genetics, Breeding, Reproduction and Molecular Design of Jiangsu Province, Yangzhou University, Yangzhou, China.
Sutai Pig Breeding Center of Jiangsu Province, Suzhou, China.
Genet Mol Res. 2014 May 9;13(2):3686-92. doi: 10.4238/2014.May.9.12.
The transporter associated with antigen processing (TAP) transports peptides from the cytosol into the endoplasmic reticulum for subsequent loading onto the major histocompatibility complex (MHC) class I molecules. This study showed the dynamic changes in the TAP1 expression level in newborn to weaning piglets. Tissue expression profiles revealed that the TAP1 gene was expressed at low levels in all tissues, and the expression levels were relatively higher in the lung, spleen, lymph, and thymus; further, no significant difference was observed in the expression in each tissue among the 3 unweaned stages (8, 18, and 30 days). Nevertheless, the postweaning (35 days) expression levels in tissues, including the spleen, lung, lymph, duodenum, and jejunum were significantly higher than those in the unweaned stages. Furthermore, gene ontology and pathway analysis showed that TAP1 took part in 38 biological functions and 5 pathway processes, including ABC transporters and antigen processing and presentation. These analyses showed that the TAP1 gene, which was related to MHC I immune regulation, had a stable and low expression level in unweaned stages; however, its expression increased in the postweaning stages. The high expression level of TAP1 indicated that the gene might play an important role in Escherichia coli F18 resistance.
与抗原加工相关的转运体(TAP)将肽从细胞质转运到内质网,以便随后加载到主要组织相容性复合体(MHC)I类分子上。本研究展示了新生仔猪到断奶仔猪TAP1表达水平的动态变化。组织表达谱显示,TAP1基因在所有组织中表达水平较低,在肺、脾、淋巴和胸腺中表达水平相对较高;此外,在3个未断奶阶段(8、18和30天)各组织中的表达未观察到显著差异。然而,断奶后(35天)脾、肺、淋巴、十二指肠和空肠等组织中的表达水平显著高于未断奶阶段。此外,基因本体论和通路分析表明,TAP1参与38种生物学功能和5种通路过程,包括ABC转运体以及抗原加工和呈递。这些分析表明,与MHC I免疫调节相关的TAP1基因在未断奶阶段表达水平稳定且较低;然而,其表达在断奶后阶段增加。TAP1的高表达水平表明该基因可能在抗大肠杆菌F18中发挥重要作用。