Zhang Tongtong, Li Qian, Li Xiaoqing, Kang Li, Jiang Yunliang, Sun Yi
Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, Shandong Agricultural University, 61 Daizong Street, Shandong Province, 271018, Taian City, People's Republic of China.
BMC Genomics. 2021 Sep 21;22(1):683. doi: 10.1186/s12864-021-07975-7.
As one of "γδ-high" species, chicken is an excellent model for the study of γδ T cells in non-mammalian animals. However, a comprehensive characterization of the TCRγδ repertoire is still missing in chicken. The objective of this study was to characterize the expressed TCRγ repertoire in chicken thymus using high-throughput sequencing.
In this study, we first obtained the detailed genomic organization of the TCRγ locus of chicken based on the latest assembly of the red jungle fowl genome sequences (GRCg6a) and then characterized the TCRγ repertoire in the thymus of four chickens by using 5' Rapid Amplification of cDNA Ends (5' RACE) along with high-throughput sequencing (HTS).
The chicken TCRγ locus contains a single Cγ gene, three functional Jγ segments and 44 Vγ segments that could be classified into six subgroups, each containing six, nineteen, nine, four, three and three members. Dot-plot analysis of the chicken TCRγ locus against itself showed that almost all the entire zone containing Vγ segments had arisen through tandem duplication events, and the main homology unit, containing 9 or 10 Vγ gene segments, has tandemly duplicated for four times. For the analysis of chicken TCRγ repertoire, more than 100,000 unique Vγ-region nucleotide sequences were obtained from the thymus of each chicken. After alignment to the germline Vγ and Jγ segments identified above, we found that the four chickens had similar repertoire profile of TCRγ. In brief, four Vγ segments (including Vγ3.7, Vγ2.13, Vγ1.6 and Vγ1.3) and six Vγ-Jγ pairs (including Vγ3.7-Jγ3, Vγ2.13-Jγ1, Vγ2.13-Jγ3, Vγ1.6-Jγ3, Vγ3.7-Jγ1 and Vγ1.6-Jγ1) were preferentially utilized by all four individuals, and vast majority of the unique CDR3γ sequences encoded 4 to 22 amino acids with mean 12.90 amino acids, which exhibits a wider length distribution and/or a longer mean length than CDR3γ of human, mice and other animal species.
In this study, we present the first in-depth characterization of the TCRγ repertoire in chicken thymus. We believe that these data will facilitate the studies of adaptive immunology in birds.
作为“γδ高表达”物种之一,鸡是研究非哺乳动物γδ T细胞的优秀模型。然而,鸡的TCRγδ库的全面特征仍不清楚。本研究的目的是利用高通量测序对鸡胸腺中表达的TCRγ库进行特征分析。
在本研究中,我们首先基于红原鸡基因组序列(GRCg6a)的最新组装获得了鸡TCRγ基因座的详细基因组结构,然后通过5' cDNA末端快速扩增(5' RACE)结合高通量测序(HTS)对四只鸡胸腺中的TCRγ库进行了特征分析。
鸡的TCRγ基因座包含一个单一的Cγ基因、三个功能性Jγ片段和44个Vγ片段,可分为六个亚组,每个亚组分别包含六个、十九个、九个、四个、三个和三个成员。鸡TCRγ基因座自身的点阵分析表明,几乎所有包含Vγ片段的整个区域都是通过串联重复事件产生的,主要的同源单位包含9或10个Vγ基因片段,已经串联重复了四次。对于鸡TCRγ库的分析,从每只鸡的胸腺中获得了超过100,000个独特的Vγ区域核苷酸序列。在与上述鉴定的种系Vγ和Jγ片段比对后,我们发现这四只鸡的TCRγ库谱相似。简而言之,四个Vγ片段(包括Vγ3.7、Vγ2.13、Vγ1.6和Vγ1.3)和六个Vγ-Jγ对(包括Vγ3.7-Jγ3、Vγ2.13-Jγ1、Vγ2.13-Jγ3、Vγ1.6-Jγ3、Vγ3.7-Jγ1和Vγ1.6-Jγ1)被所有四个个体优先利用,并且绝大多数独特的CDR3γ序列编码4至22个氨基酸,平均为12.90个氨基酸,与人类、小鼠和其他动物物种的CDR3γ相比,其长度分布更宽和/或平均长度更长。
在本研究中,我们首次对鸡胸腺中的TCRγ库进行了深入表征。我们相信这些数据将有助于鸟类适应性免疫学的研究。