High-throughput mutagenesis identifies mutations and RNA-binding proteins controlling CD19 splicing and CART-19 therapy resistance

Nat Commun. 2022 Sep 22;13(1):5570. doi: 10.1038/s41467-022-31818-y.

Abstract

Following CART-19 immunotherapy for B-cell acute lymphoblastic leukaemia (B-ALL), many patients relapse due to loss of the cognate CD19 epitope. Since epitope loss can be caused by aberrant CD19 exon 2 processing, we herein investigate the regulatory code that controls CD19 splicing. We combine high-throughput mutagenesis with mathematical modelling to quantitatively disentangle the effects of all mutations in the region comprising CD19 exons 1-3. Thereupon, we identify ~200 single point mutations that alter CD19 splicing and thus could predispose B-ALL patients to developing CART-19 resistance. Furthermore, we report almost 100 previously unknown splice isoforms that emerge from cryptic splice sites and likely encode non-functional CD19 proteins. We further identify cis-regulatory elements and trans-acting RNA-binding proteins that control CD19 splicing (e.g., PTBP1 and SF3B4) and validate that loss of these factors leads to pervasive CD19 mis-splicing. Our dataset represents a comprehensive resource for identifying predictive biomarkers for CART-19 therapy.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing / genetics
  • Antigens, CD19 / genetics
  • Antigens, CD19 / metabolism
  • Epitopes / metabolism
  • Heterogeneous-Nuclear Ribonucleoproteins / metabolism
  • Humans
  • Mutagenesis / genetics
  • Mutation
  • Neoplasm Recurrence, Local / genetics
  • Polypyrimidine Tract-Binding Protein / genetics
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma* / genetics
  • Protein Isoforms / genetics
  • RNA Splice Sites*
  • RNA Splicing
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism

Substances

  • Antigens, CD19
  • Epitopes
  • Heterogeneous-Nuclear Ribonucleoproteins
  • PTBP1 protein, human
  • Protein Isoforms
  • RNA Splice Sites
  • RNA-Binding Proteins
  • Polypyrimidine Tract-Binding Protein