Igh and Igk loci use different folding principles for V gene recombination due to distinct chromosomal architectures of pro-B and pre-B cells.
Louisa HillGordana WutzMarkus JaritzHiromi TagohLesly CalderónJan-Michael PetersAnton GoloborodkoMeinrad BusslingerPublished in: Nature communications (2023)
Extended loop extrusion across the immunoglobulin heavy-chain (Igh) locus facilitates V H -DJ H 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 K -J K 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 K and J K elements to facilitate V K -J K 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 H genes and likely to allelic exclusion of all other V H 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.
Keyphrases
- dna damage
- genome wide
- copy number
- dna repair
- genome wide association study
- transcription factor
- high resolution
- poor prognosis
- anti inflammatory
- gene expression
- cell proliferation
- genome wide identification
- single molecule
- signaling pathway
- mass spectrometry
- molecular dynamics simulations
- binding protein
- high speed
- wild type