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人免疫球蛋白重链可变区基因的特征分析

Characterization of the Heavy Chain Variable Region Gene of Human Immunoglobulins
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摘要 目的:分析五类免疫球蛋白重链可变区基因的特征.方法:收集IMGT/LIGM-DB数据库中人类五类Ig重链可变区的基因序列,利用IMGT/HighV-QUEST分析其基因取用、V区AA变化、CDR3氨基酸长度和构成以及连接多样性.结果:IgM、IgG和IgE均较多地取用IGHJ4、IGHV1-69和IGHV5-51,且在IgM、IgG、IgA与IgE中可观察到几个相似的优势V-J配对.IgD具有较高的V区突变,主要体现在FR3区的高突变(AA变化值为7.2±2.4),而IgM的每个结构域的突变均明显低于其他类Ig.此外,IgD具有较高P插入发生率和插入核苷酸数明显多于其他四类Ig.结论:本研究从基因特征上描绘了人类五类Ig相互间的相似性与差异性,这些结果可为抗体工程领域提供重要参考数据. Objective: To analyze the characteristics of five types of immunoglobulin heavy chain variable region genes.Method: The gene sequences of the heavy chain variable regions of human Ig were obtained from the IMGT/LIGM-DB database.An extensive analysis of these genes was implemented using IMGT/HighV-QUEST, including gene usage, amino acid (AA)changes in V region, length distribution and composition of CDR3 amino acid and junctional diversity.Results: IGHJ4, IGHV1-69 and IGHV5-51 were more frequently used in IgM, IgG and IgE.And several similar superior V-J pairings were observed in IgM, IgG, IgA and IgE.There was a higher mutation level of V region in IgD which mainly reflected in FR3 region (number of AA changes=7.2±2.4), while the mutations in each domain of IgM were significantly lower than those of other Igs.In addition, IgD has a higher incidence of P insertion and a higher number of nucleotides than other Igs.Conclusion: This study describes the similarities and differences among human five types of Ig from the genetic characteristics.These results can provide important reference data for the field of antibody engineering.
作者 石彬 马嘉欣 涂文静 吴皓明 陈先恋 SHI Bin;MA Jia-xin;TU Wen-jing;WU Hao-ming;CHEN Xian-lian(Department of Laboratory Medicine, The First Afliated Hospital of Zunyi Medical University, Zunyi 563000, China;School of Laboratory Medicine, Zunyi Medical University, Zunyi 563000, China)
出处 《聊城大学学报(自然科学版)》 2019年第4期11-17,共7页 Journal of Liaocheng University:Natural Science Edition
基金 国家自然科学基金项目(81760300)资助
关键词 IG 重链可变区基因 CDR3 IMGT/LIGM-DB Ig heavy chain variable region gene CDR3 IMGT/LIGM-DB
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