Al Hayek Sandy, Praité Antoine, Lambert Jean-Marie, Bender Sébastien, Delpy Laurent
UMR CNRS 7276, Inserm 1262, Université de Limoges, Limoges, France; CRIBL lab (Control of the B-cell Immune Response and Lymphoproliferations), Limoges, France; Team 3, BioPIC (Biology of Plasma Cells, Immunopathology and Cancer), Limoges, France.
Université Côte d'Azur, CNRS, Molecular and Cellular Pharmacology Institute, Valbonne, France.
Methods Mol Biol. 2025;2962:103-119. doi: 10.1007/978-1-0716-4726-4_8.
This chapter outlines a detailed methodology for high-throughput sequencing of the immunoglobulin (Ig) repertoire from mouse RNA samples. We describe RNA extraction from splenic B cells, followed by the conversion into cDNA using the 5'RACE (Rapid Amplification of cDNA Ends) technique and PCR amplification of the Ig heavy and light chain repertoire. The amplified products are prepared using specific primers for Illumina next-generation sequencing (NGS) and unique molecular identifiers (UMI) as molecular barcodes. The protocol includes stringent quality control steps to ensure the integrity of RNA and the accuracy of amplification. We describe the amplification of Ighm and all Ighg subclasses, for Ig heavy chains and for the predominant Igκ light chain isotype. RNA-based 5'RACE-RepSeq proves very useful to analyze the diversity and clonality of Ig repertoire, as well as somatic hypermutations, providing insights into the adaptive immune response. This method enables the high-throughput characterization of the mouse Ig repertoire in immunological contexts.
本章概述了从小鼠RNA样本中对免疫球蛋白(Ig)库进行高通量测序的详细方法。我们描述了从脾B细胞中提取RNA,随后使用5'RACE(cDNA末端快速扩增)技术将其转化为cDNA,并对Ig重链和轻链库进行PCR扩增。使用针对Illumina下一代测序(NGS)的特异性引物和作为分子条形码的独特分子标识符(UMI)来制备扩增产物。该方案包括严格的质量控制步骤,以确保RNA的完整性和扩增的准确性。我们描述了Ighm和所有Ighg亚类、Ig重链以及主要的Igκ轻链同种型的扩增。基于RNA的5'RACE-RepSeq在分析Ig库的多样性和克隆性以及体细胞超突变方面非常有用,有助于深入了解适应性免疫反应。该方法能够在免疫背景下对小鼠Ig库进行高通量表征。