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New alleles of chicken CD8 alpha and CD3d found in Chinese native and western breeds

机译:在中国本土和西方品种中发现的鸡CD8 alpha和CD3d新等位基因

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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.
机译:中国本土鸡品种为研究遗传多样性提供了有用的资源。在这项研究中,从序列水平分析了中国本土和引进的西方鸡品种的CD8α和CD3d cDNA等位基因。由于CD8 alpha序列的胞外域中有13个氨基酸置换,因此发现了6个等位基因。在中国菌株中检测到四个等位基因,并且首次鉴定了等位基因5和6。 Lang山,北京胖子和隐性白羽鸡共享了等位基因6。在Bigbone品系中发现的等位基因2与在来克霍恩品系H.B15.H7中发现的等位基因相同,在仙居品种中的等位基因3也与来克霍恩品系H.B15.H12中的发现相同。两条来克霍恩线(RPL线7和AY519197)和山茶花分别具有等位基因(等位基因1、4和5),而在其他品系中则没有。 13个氨基酸替换中的9个位于假定的I类主要组织相容性复合物(MHC)结合CDR1(位置30、33和34),CDR2(位置58、62、63和65)和CDR3(位置90和106)。 。除鲜菊品种外,中国本土鸡品种的CD8 alpha cDNA具有高度同源性。在CD3d中发现了两个等位基因。在新发现的等位基因2中的64、65和66位上发现了3个其他核苷酸。这导致了古氏CD3d cDNA胞外域中4个氨基酸(第22、23、24和25位残基)的差异,隐性白羽和ISA鸡与白来亨鸡和T11.15(NM_205512)相比。通过DNA免疫产生了针对鸡CD8α的五个杂交瘤克隆(1C9、1H5、4B11、6G5和13C5)。两种单克隆抗体(Gab)6G5和4B11对五个中国本土鸡品种隐性白羽鸡和来克亨鸡(AY519197)的脾细胞有反应性,而单克隆抗体1C9、1H5和13C5与这些品种没有反应。

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