Different classes of genomic inserts contribute to human antibody diversity

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Publikace nespadá pod Ústav výpočetní techniky, ale pod Středoevropský technologický institut. Oficiální stránka publikace je na webu muni.cz.
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LEBEDIN Mikhail FOGLIERINI Mathilde KHORKOVA Svetlana GARCIA Clara Vazquez RATSWOHL Christoph DAVYDOV Alexey Nikolayevich TURCHANINOVA Maria A DAUBENBERGER Claudia CHUDAKOV Dmitriy LANZAVECCHIA Antonio KATHRIN de la Rosa

Rok publikování 2022
Druh Článek v odborném periodiku
Časopis / Zdroj Proceedings of the National Academy of Sciences of the United States of America
Fakulta / Pracoviště MU

Středoevropský technologický institut

Citace
www https://www.pnas.org/doi/full/10.1073/pnas.2205470119
Doi http://dx.doi.org/10.1073/pnas.2205470119
Klíčová slova B cell diversity; antibody repertoire; insert
Popis Recombination of antibody genes in B cells can involve distant genomic loci and contribute a foreign antigen-binding element to form hybrid antibodies with broad reactivity for Plasmodium falciparum. So far, antibodies containing the extracellular domain of the LAIR1 and LILRB1 receptors represent unique examples of cross-chromosomal antibody diversification. Here, we devise a technique to profile non-VDJ elements from distant genes in antibody transcripts. Independent of the preexposure of donors to malaria parasites, non-VDJ inserts were detected in 80% of individuals at frequencies of 1 in 10(4) to 10(5) B cells. We detected insertions in heavy, but not in light chain or T cell receptor transcripts. We classify the insertions into four types depending on the insert origin and destination: 1) mitochondrial and 2) nuclear DNA inserts integrated at VDJ junctions; 3) inserts originating from telomere proximal genes; and 4) fragile sites incorporated between J-to-constant junctions. The latter class of inserts was exclusively found in memory and in in vitro activated B cells, while all other classes were already detected in naive B cells. More than 10% of inserts preserved the reading frame, including transcripts with signs of antigen-driven affinity maturation. Collectively, our study unravels a mechanism of antibody diversification that is layered on the classical V(D)J and switch recombination.
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