Zheng Wenbiao, Liu Guozhu, Ao Jingqun, Chen Xinhua
Department of Biology, School of Life Science, Xiamen University, Xiamen 361005, PR China.
Fish Shellfish Immunol. 2006 Oct;21(4):414-30. doi: 10.1016/j.fsi.2006.01.006. Epub 2006 Apr 5.
A SMART cDNA library from spleen of large yellow croaker (Pseudosciaena crocea) stimulated by poly I:C was constructed. A total of 1039 clones from the library were single-pass sequenced and compared with known sequences in the GenBank database. Of those expressed sequence tags (ESTs), 607 were identified as orthologs of known genes in the GenBank databases by Blast X search. Four hundred and thirty-two did not show significant homology with any known sequences in the public databases. These identified ESTs represented at least 252 different genes, which were categorised into nine groups according to their function. Of the identified genes, 159 genes (63.1%) shared homology with fish genes while 93 (36.9%) showed the highest homology to the genes from other species. Forty-six genes were identified to be involved in immune functions, including complement system components, immunoglobulins, antigen processing and presentation proteins, interferon system proteins, cytokines, and some innate defence molecules. The most frequently occurring genes in this spleen cDNA library were hepcidin precursors represented by 46 ESTs, which were divided into five groups based on their putative amino acid sequences. The expression analysis of selected genes during polyI:C induction was performed by reverse transcription-PCR (RT-PCR), including Mx protein, beta2-microglobulin (beta(2)m), CD2 binding protein 1(CD2BP1), placenta-specific 8 genes, MHC class II associated invariant chain (li) and cytochrome b-245 alpha peptide (Cyba). The results revealed that expression levels of Mx protein, beta(2)m, placenta-specific 8 genes, and Cyba were significantly upregulated at 30h after induction with poly I:C, and the CD2BP1 expression was also induced by polyI:C, suggesting that these genes may be involved in an immune response induced by poly I:C in large yellow croaker.
构建了经聚肌胞苷酸(poly I:C)刺激的大黄鱼脾脏的SMART cDNA文库。对该文库中的1039个克隆进行了单通道测序,并与GenBank数据库中的已知序列进行了比较。在这些表达序列标签(EST)中,通过Blast X搜索,607个被鉴定为GenBank数据库中已知基因的直系同源物。432个与公共数据库中的任何已知序列均无显著同源性。这些鉴定出的EST代表了至少252个不同的基因,根据其功能分为九组。在鉴定出的基因中,159个基因(63.1%)与鱼类基因具有同源性,而93个(36.9%)与其他物种的基因具有最高同源性。46个基因被鉴定参与免疫功能,包括补体系统成分、免疫球蛋白、抗原加工和呈递蛋白、干扰素系统蛋白、细胞因子以及一些先天防御分子。该脾脏cDNA文库中出现频率最高的基因是由46个EST代表的铁调素前体,根据其推测的氨基酸序列分为五组。通过逆转录PCR(RT-PCR)对polyI:C诱导过程中选定基因的表达进行了分析,包括Mx蛋白、β2-微球蛋白(β(2)m)、CD2结合蛋白1(CD2BP1)、胎盘特异性8基因、MHC II类相关恒定链(li)和细胞色素b-245α肽(Cyba)。结果显示,poly I:C诱导30小时后,Mx蛋白、β(2)m、胎盘特异性8基因和Cyba的表达水平显著上调,CD2BP1的表达也被polyI:C诱导,表明这些基因可能参与了大黄鱼中poly I:C诱导的免疫反应。