
Wapl repression by Pax5 promotes V gene recombination by Igh loop extrusion
Author(s) -
Louisa Hill,
Anja Ebert,
Markus Jaritz,
Gordana Wutz,
Kota Nagasaka,
Hiromi Tagoh,
Daniela Kostanova-Poliakova,
Karina Schindler,
Qiong Sun,
Peter Bönelt,
Maria Fischer,
JanMichael Peters,
Meinrad Busslinger
Publication year - 2020
Publication title -
nature
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 15.993
H-Index - 1226
eISSN - 1476-4687
pISSN - 0028-0836
DOI - 10.1038/s41586-020-2454-y
Subject(s) - chromatin , pax5 , cohesin , bivalent chromatin , microbiology and biotechnology , immunoglobulin class switching , psychological repression , biology , gene , genetics , nucleosome , b cell , transcription factor , gene expression , antibody
Nuclear processes, such as V(D)J recombination, are orchestrated by the three-dimensional organization of chromosomes at multiple levels, including compartments 1 and topologically associated domains (TADs) 2,3 consisting of chromatin loops 4 . TADs are formed by chromatin-loop extrusion 5-7 , which depends on the loop-extrusion function of the ring-shaped cohesin complex 8-12 . Conversely, the cohesin-release factor Wapl 13,14 restricts loop extension 10,15 . The generation of a diverse antibody repertoire, providing humoral immunity to pathogens, requires the participation of all V genes in V(D)J recombination 16 , which depends on contraction of the 2.8-Mb-long immunoglobulin heavy chain (Igh) locus by Pax5 17,18 . However, how Pax5 controls Igh contraction in pro-B cells remains unknown. Here we demonstrate that locus contraction is caused by loop extrusion across the entire Igh locus. Notably, the expression of Wapl is repressed by Pax5 specifically in pro-B and pre-B cells, facilitating extended loop extrusion by increasing the residence time of cohesin on chromatin. Pax5 mediates the transcriptional repression of Wapl through a single Pax5-binding site by recruiting the polycomb repressive complex 2 to induce bivalent chromatin at the Wapl promoter. Reduced Wapl expression causes global alterations in the chromosome architecture, indicating that the potential to recombine all V genes entails structural changes of the entire genome in pro-B cells.