Research Institute of Molecular Pathology (IMP), Vienna BioCenter (VBC), Campus-Vienna-Biocenter 1, A-1030, Vienna, Austria.
Institute of Molecular Biotechnology (IMBA), Austrian Academy of Sciences, Vienna BioCenter (VBC), Dr. Bohr-Gasse 3, A-1030, Vienna, Austria.
Nat Commun. 2023 Apr 21;14(1):2316. doi: 10.1038/s41467-023-37994-9.
Extended loop extrusion across the immunoglobulin heavy-chain (Igh) locus facilitates V-DJ 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-J 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 and J elements to facilitate V-J 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 genes and likely to allelic exclusion of all other V 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.
免疫球蛋白重链(Igh)基因座上的延伸环挤压通过 Pax5 下调黏合释放因子 Wapl 促进 V-DJ 重组,导致前 B 细胞中染色体结构的整体变化。在这里,我们证明 Igk 基因座上的染色质环挤压和 V-J 重组对 pre-B 细胞中 Wapl 的上调不敏感。值得注意的是,Wapl 蛋白在前 B 细胞中的表达水平比在 pro-B 细胞中高 2.2 倍,这导致 pre-B 细胞中的染色体结构具有正常的环大小。对 Igk 基因座的高分辨率染色体接触分析确定了多个内部环,这些环可能将 V 和 J 元件并置以促进 V-J 重组。在 Igμ-转基因前 B 细胞中,Wapl 的高表达阻止了 Igh 基因座上的延伸环挤压,导致仅重组 6 个最 3'近端 V 基因,并且可能在前 B 细胞中排除所有其他 V 基因的等位基因排斥。这些结果表明,具有不同染色体结构的 pro-B 和 pre-B 细胞使用不同的染色质折叠原则进行 V 基因重组,从而在前 B 细胞中 Igk 基因座重组时实现 Igh 基因座的等位基因排斥。