Hu Qinghai, Pan Zhiming, Deen Shovel, Meng Songshu, Zhang Xueyu, Zhang Xiaoyan, Jiao Xin-an
College of Veterinary Medicine, Yangzhou University, 12 East Wenhui Road, Yangzhou, Jiangsu 225009, China.
Vet Immunol Immunopathol. 2007 Dec 15;120(3-4):223-33. doi: 10.1016/j.vetimm.2007.08.008. Epub 2007 Aug 25.
Chinese native chicken breeds provide useful resources for the study of genetic diversity. In this study, the alleles of CD8 alpha and CD3d cDNA from Chinese native and introduced western breeds of chicken were analyzed at the sequence level. Six alleles were found, due to 13 amino acid replacements in the extracellular domain of the CD8 alpha sequence. There were four alleles detected in the Chinese strains, and alleles 5 and 6 were identified for the first time. Allele 6 was shared by Langshan, Beijing Fatty and Recessive White Feather chickens. Allele 2, found in the Bigbone strain, was the same as that found in the Leghorn strain H.B15.H7, and allele 3 in the Xianju breed was also the same as in the Leghorn strain H.B15.H12. Two Leghorn lines (RPL line 7 and AY519197) and the Camellia possessed an allele (alleles 1, 4 and 5), respectively, that was not found in the other lines. Nine out of 13 amino acid replacements were situated in the putative major histocompatibility complex (MHC) class I binding CDR1 (positions 30, 33 and 34), CDR2 (positions 58, 62, 63 and 65) and CDR3 (positions 90 and 106). Except for the Xianju breed, the CD8 alpha cDNA of Chinese native chicken breeds shared high homology. Two alleles were found in CD3d. Three additional nucleotides were found at positions 64, 65 and 66 in the newly discovered allele 2. This led to a difference of four amino acids (at residues 22, 23, 24 and 25) in the extracellular domain of CD3d cDNA from the Gushi, Recessive White Feather and ISA chickens compared with these of the White Leghorn and T11.15 (NM_205512). Five hybridoma clones (1C9, 1H5, 4B11, 6G5 and 13C5) against chicken CD8 alpha were generated by DNA immunization. Two monoclonal antibodies (mAbs), 6G5 and 4B11, showed reactivity to the splenocytes from five Chinese native chicken breeds, the Recessive White Feather chicken and the Leghorn (AY519197), while mAbs 1C9, 1H5 and 13C5 showed no reaction with these breeds.
中国本土鸡品种为遗传多样性研究提供了有用资源。在本研究中,对中国本土鸡品种和引进的西方鸡品种的CD8α和CD3d cDNA等位基因进行了序列水平分析。由于CD8α序列胞外域中有13个氨基酸替换,共发现6个等位基因。在中国品系中检测到4个等位基因,等位基因5和6为首次鉴定。等位基因6在狼山鸡、北京油鸡和隐性白羽鸡中共有。在大骨鸡品系中发现的等位基因2与来航鸡品系H.B15.H7中发现的相同,仙居鸡品种中的等位基因3也与来航鸡品系H.B15.H12中的相同。两个来航鸡品系(RPL品系7和AY519197)和茶花鸡分别拥有一个在其他品系中未发现的等位基因(等位基因1、4和5)。13个氨基酸替换中有9个位于假定的主要组织相容性复合体(MHC)I类结合的CDR1(第30、33和34位)、CDR2(第58、62、63和65位)和CDR3(第90和106位)。除仙居鸡品种外,中国本土鸡品种的CD8α cDNA具有高度同源性。在CD3d中发现了2个等位基因。在新发现的等位基因2的第64、65和66位发现了另外3个核苷酸。这导致固始鸡、隐性白羽鸡和ISA鸡的CD3d cDNA胞外域与白来航鸡和T11.15(NM_205512)相比,在4个氨基酸(第22、23、24和25位残基)上存在差异。通过DNA免疫产生了5个抗鸡CD8α的杂交瘤克隆(1C9、1H5、4B11、6G5和13C5)。两种单克隆抗体(mAb),6G5和4B11,对5个中国本土鸡品种、隐性白羽鸡和来航鸡(AY519197)的脾细胞有反应,而mAb 1C9、1H5和13C5对这些品种无反应。