# The splicing factor PTBP1 interacts with RUNX1 and is required for leukemia cell survival

## TL;DR

This study shows that the splicing factor PTBP1 interacts with RUNX1 and is crucial for the survival of leukemia cells by regulating metabolic genes.

## Contribution

The novel contribution is identifying PTBP1 as a RUNX1 interactor and demonstrating its role in leukemia cell survival through RNA splicing and metabolic regulation.

## Key findings

- PTBP1 interacts with RUNX1 in an HDAC1-dependent manner and co-occupies promoter regions of actively transcribed genes.
- Loss of PTBP1 disrupts RNA splicing and reduces expression of metabolic genes, impairing leukemia cell metabolism and survival.

## Abstract

Runt-related Transcription Factor 1 (RUNX1) is essential for definitive hematopoiesis and is among the most frequently mutated genes in leukemia. Previous work from our lab demonstrated that Histone Deacetylase 1 (HDAC1), a known RUNX1 partner, is unexpectedly required for active transcription suggesting a non-histone role for HDAC1 in regulating components of the RUNX1 complex. Here, we use proteomics, genomics, and long-read transcriptomics to identify novel RUNX1 interacting partners and decipher their role in gene regulation and RNA splicing in leukemia cells. We demonstrate that Polypyrimidine Tract Binding Protein 1 (PTBP1) interacts with RUNX1 in an HDAC1-dependent manner. Chromatin profiling revealed extensive genome-wide overlap in sites occupied by RUNX1 and PTBP1, with significant enrichment at promoters of actively transcribed genes. Loss of PTBP1 in AML cells led to widespread alterations in RNA splicing and decreased expression of genes whose promoters are bound by both factors, including metabolic genes. In agreement with these findings, we found that loss of PTBP1 reduced glycolysis and glucose uptake and ultimately caused cell death. Based on our data, we propose that the interaction between RUNX1 and PTBP1 facilitates expression of metabolic proteins essential for leukemia cell growth and survival.