Germline polymorphisms and alternative splicing of human immunoglobulin light chain genes
Ivana Mikocziova,
Ayelet Peres,
Moriah Gidoni,
Victor Greiff,
Gur Yaari,
Ludvig M. Sollid
Affiliations
Ivana Mikocziova
K.G. Jebsen Centre for Coeliac Disease Research, Institute of Clinical Medicine, University of Oslo, 0372 Oslo, Norway; Department of Immunology, Oslo University Hospital, 0372 Oslo, Norway
Ayelet Peres
Faculty of Engineering, Bar Ilan University, Ramat Gan 5290002, Israel; Bar Ilan Institute of Nanotechnologies and Advanced Materials, Bar Ilan University, Ramat Gan 5290002, Israel
Moriah Gidoni
Faculty of Engineering, Bar Ilan University, Ramat Gan 5290002, Israel
Victor Greiff
Department of Immunology, Oslo University Hospital, 0372 Oslo, Norway
Gur Yaari
Faculty of Engineering, Bar Ilan University, Ramat Gan 5290002, Israel; Bar Ilan Institute of Nanotechnologies and Advanced Materials, Bar Ilan University, Ramat Gan 5290002, Israel
Ludvig M. Sollid
K.G. Jebsen Centre for Coeliac Disease Research, Institute of Clinical Medicine, University of Oslo, 0372 Oslo, Norway; Department of Immunology, Oslo University Hospital, 0372 Oslo, Norway; Corresponding author
Summary: Inference of germline polymorphisms in immunoglobulin genes from B cell receptor repertoires is complicated by somatic hypermutations, sequencing/PCR errors, and by varying length of reference alleles. The light chain inference is particularly challenging owing to large gene duplications and absence of D genes. We analyzed the light chain cDNA sequences from naïve B cell receptor repertoires from 100 individuals. We optimized light chain allele inference by tweaking parameters of the TIgGER functions, extending the germline reference sequences, and establishing mismatch frequency patterns at polymorphic positions to filter out false-positive candidates. We identified 48 previously unreported variants of light chain variable genes. We selected 14 variants for validation and successfully validated 11 by Sanger sequencing. Clustering of light chain 5′UTR, L-PART1, and L-PART2 revealed partial intron retention in 11 kappa and 9 lambda V alleles. Our results provide insight into germline variation in human light chain immunoglobulin loci.
