Igh and Igk loci use different folding principles for V gene recombination due to distinct chromosomal architectures of pro-B and pre-B cells.

Hill, Louisa; Wutz, Gordana; Jaritz, Markus; Tagoh, Hiromi; Calderón, Lesly; Peters, Jan-Michael; Goloborodko, Anton; Busslinger, Meinrad · Nat Commun · 2023

basic_science · Level V

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Abstract

Extended loop extrusion across the immunoglobulin heavy-chain (Igh) locus facilitates V<sub>H</sub>-DJ<sub>H</sub> recombination following downregulation of the cohesin-release factor Wapl by Pax5, resulting in global changes in the chromosomal architecture of pro-B cells. Here, we demonstrate that chromatin looping and V<sub>K</sub>-J<sub>K</sub> recombination at the Igk locus were insensitive to Wapl upregulation in pre-B cells. Notably, the Wapl protein was expressed at a 2.2-fold higher level in pre-B cells compared with pro-B cells, which resulted in a distinct chromosomal architecture with normal loop sizes in pre-B cells. High-resolution chromosomal contact analysis of the Igk locus identified multiple internal loops, which likely juxtapose V<sub>K</sub> and J<sub>K</sub> elements to facilitate V<sub>K</sub>-J<sub>K</sub> recombination. The higher Wapl expression in Igμ-transgenic pre-B cells prevented extended loop extrusion at the Igh locus, leading to recombination of only the 6 most 3' proximal V<sub>H</sub> genes and likely to allelic exclusion of all other V<sub>H</sub> genes in pre-B cells. These results suggest that pro-B and pre-B cells with their distinct chromosomal architectures use different chromatin folding principles for V gene recombination, thereby enabling allelic exclusion at the Igh locus, when the Igk locus is recombined.

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