Igh and Igk loci use different folding principles for V gene recombination due to distinct chromosomal architectures of pro-B and pre-B cells.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 37085514.
- Also identified by DOI 10.1038/s41467-023-37994-9 and PMC identifier 10121685.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
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.
Medical subject headings
- Immunoglobulin Heavy Chains
- Precursor Cells, B-Lymphoid
- V(D)J Recombination