Identification of IgG1 and IgG3 Allotypes by PCR and Sanger Sequencing.

Methods Mol Biol

Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, VIC, Australia.

Published: July 2024

AI Article Synopsis

  • The IGHG gene cluster encodes for different subclasses of immunoglobulin G (IgG) and is known for its high polymorphism, leading to various allotypes in humans.
  • IGHG1 and IGHG3 are the most variable subclasses, with multiple allotypes, and recent studies have highlighted greater diversity in specific ethnic groups.
  • The text outlines a detailed protocol for using PCR and Sanger sequencing to amplify IGHG gene segments and analyze SNPs linked to different allotypes of IgG1 and IgG3.

Article Abstract

The immunoglobulin heavy constant gamma (IGHG) gene cluster encoding immunoglobulin G (IgG) subclasses is highly polymorphic, resulting in amino acid variation along the antibody constant heavy chain referred to as allotypes. IGHG1 and IGHG3 are the two most polymorphic IgG subclasses in humans, with 4 classical IgG1 allotypes and 13 allotypes described for IgG3, though recent studies suggest greater allelic diversity, especially in underrepresented ethnic populations. Polymerase chain reaction (PCR) and Sanger sequencing of IGHG amplicons allow for the identification of the single nucleotide polymorphisms (SNPs) responsible for the observed amino acid substitutions. Here, we provide a detailed protocol for the amplification of IGHG1 and IGHG3 segments by PCR, sample preparation for Sanger sequencing, and analysis of sequencing data to identify SNPs associated with different IgG1 and IgG3 allotypes.

Download full-text PDF

Source
http://dx.doi.org/10.1007/978-1-0716-3950-4_15DOI Listing

Publication Analysis

Top Keywords

sanger sequencing
12
igg1 igg3
8
igg3 allotypes
8
pcr sanger
8
igg subclasses
8
amino acid
8
ighg1 ighg3
8
allotypes
5
identification igg1
4
allotypes pcr
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!