HnRNP A1 and A2B1 enforce Ezh2 mRNA splicing to promote germinal center B cell responses

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HnRNP A1 and A2B1 enforce Ezh2 mRNA splicing to promote germinal center B cell responses
Title:
HnRNP A1 and A2B1 enforce Ezh2 mRNA splicing to promote germinal center B cell responses
Journal Title:
Nature Communications
Keywords:
Publication Date:
11 June 2026
Citation:
Zhu, Z., Zhang, R., Kang, H., Chen, M., Huang, H., Wang, J., Guo, L., Li, Y., Chen, W., Meng, L., Wang, R., Li, L., Lam, K.-P., Xu, S., & Ou, X. (2026). HnRNP A1 and A2B1 enforce Ezh2 mRNA splicing to promote germinal center B cell responses. Nature Communications. https://doi.org/10.1038/s41467-026-74159-w
Abstract:
Heterogeneous nuclear ribonucleoproteins (hnRNP) are key regulators of gene expression, yet the physiological functions of the highly homologous hnRNP A1 and A2B1 in B cells remain unclear. Here, we conditionally delete Hnrnpa1 and Hnrnpa2b1 in mouse B cells and find that loss of hnRNP A1 and A2B1 compromises the germinal center (GC) reaction during T cell-dependent immune responses. Loss of hnRNP A1 and A2B1 impairs GC B cell proliferation and high-affinity antibody production. Mechanistically, hnRNP A1/A2B1 bind UAG-rich motifs in Ezh2 pre-mRNA to promote Ezh2 exon 14 inclusion, thereby preserving EZH2 catalytic activity; in their absence, Ezh2 exon 14-skipping produces a catalytically inactive EZH2 isoform (Ezh2Δ14) with diminished repression of the cell cycle inhibitor Cdkn1a. The resulting CDKN1A accumulation restricts B cell proliferation, while Cdkn1a deletion partially rescues the GC defects in B cells deficient for hnRNP A1 and A2B1. Our findings thus uncover an hnRNP A1/A2B1–EZH2–CDKN1A axis that integrates RNA splicing with epigenetic regulation of B cell immunity.
License type:
Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
Funding Info:
This research is supported by core funding from: A*STAR Singapore Immunology Network (A*STAR SIgN)
Grant Reference no. : NA
Description:
ISSN:
2041-1723