Wu Mingli, Chen Fuwen, Tang Xiaoqin, Li Jingxuan, Zhao Haidong, Zhang Yuelang
Guangxi Key Laboratory of Brain and Cognitive Neuroscience, Guilin Medical University, Guilin, Guangxi, China.
Hainan Institute of Zhejiang University, Sanya, Hainan, China.
Front Immunol. 2025 Aug 29;16:1643380. doi: 10.3389/fimmu.2025.1643380. eCollection 2025.
As an important livestock species, sheep exhibit remarkable environmental adaptability. Immunoglobulins, expressed by B cells, are among the most crucial effector molecules in adaptive immunity. However, systematic research on the structure and expression diversity of the sheep immunoglobulins gene loci remains limited. This study annotated the sheep IgH, Igκ, and Igλ loci based on the sheep genome assembly (ARS-UI_Ramb_v3.0). The sheep IgH is located on chromosome 18 and comprises 22 VH, 4 DH, and 6 JH. The Igκ is on chromosome 3, containing 18 Vκ and 4 Jκ. The Igλ is situated on chromosome 17 and consists of 128 Vλ and 3 Jλ. Rearranged IgH, Igκ, and Igλ sequences were obtained from sheep spleen using 5' RACE PCR. Following PE300 high-throughput sequencing, we analyzed the diversity of V, D, J expression diversity, V(D)J recombination, junctional diversity, and somatic hypermutation in the rearranged sequences. For IgH rearrangement, 4 VH, 4 DH, and 2 JH gene segments were utilized, generating 26 distinct rearrangement types. Igκ rearrangement employed 5 Vκ and 3 Jκ gene segments, resulting in 13 rearrangement types. Igλ rearrangement involved 26 Vλ and 2 Jλ gene segments, producing 28 rearrangement types. Average length of sheep CDR3H is 44 bp (maximum 66 bp), CDR3κ averages 27 bp (maximum 48 bp), and CDR3λ averages 30 bp (maximum 47 bp). N-nucleotide additions contributed more significantly to CDR3 diversity than P-nucleotides in both Igκ and Igλ rearrangements. Simultaneously, 3' V-deletion and 5' J-deletion further enriched CDR3 diversity. SHM, especially the hotspot mutation motifs, enriches the diversity caused by the V gene segments. Thus, sheep enrich immunoglobulin diversity through both junctional diversity-driven CDR3 diversification and high-intensity SHM. This study expands our understanding of the sheep immunoglobulin gene loci and their expression diversity, providing theoretical foundation for research on immunoglobulin gene evolution within the Bovidae family.
作为一种重要的家畜物种,绵羊表现出显著的环境适应性。B细胞表达的免疫球蛋白是适应性免疫中最关键的效应分子之一。然而,关于绵羊免疫球蛋白基因座的结构和表达多样性的系统研究仍然有限。本研究基于绵羊基因组组装(ARS-UI_Ramb_v3.0)对绵羊IgH、Igκ和Igλ基因座进行了注释。绵羊IgH位于18号染色体上,包含22个VH、4个DH和6个JH。Igκ位于3号染色体上,包含18个Vκ和4个Jκ。Igλ位于17号染色体上,由128个Vλ和3个Jλ组成。使用5'RACE PCR从绵羊脾脏中获得重排的IgH、Igκ和Igλ序列。经过PE300高通量测序后,我们分析了重排序列中V、D、J表达多样性、V(D)J重组、连接多样性和体细胞超突变的多样性。对于IgH重排,使用了4个VH、4个DH和2个JH基因片段,产生了26种不同的重排类型。Igκ重排使用了5个Vκ和3个Jκ基因片段,产生了13种重排类型。Igλ重排涉及26个Vλ和2个Jλ基因片段,产生了28种重排类型。绵羊CDR3H的平均长度为44bp(最大66bp),CDR3κ平均为27bp(最大48bp),CDR3λ平均为30bp(最大47bp)。在Igκ和Igλ重排中,N-核苷酸的添加对CDR3多样性的贡献比P-核苷酸更显著。同时,3'V缺失和5'J缺失进一步丰富了CDR3多样性。体细胞超突变,尤其是热点突变基序,丰富了由V基因片段引起的多样性。因此,绵羊通过连接多样性驱动的CDR3多样化和高强度的体细胞超突变来丰富免疫球蛋白多样性。本研究扩展了我们对绵羊免疫球蛋白基因座及其表达多样性的理解,为牛科动物免疫球蛋白基因进化的研究提供了理论基础。