# Molecular interactome of HNRNPU reveals regulatory networks in neuronal differentiation and DNA methylation

**Authors:** Marika Oksanen, Francesca Mastropasqua, Krystyna Mazan-Mamczarz, Jennifer L Martindale, Xuan Ye, Abishek Arora, Nirad Banskota, Myriam Gorospe, Kristiina Tammimies

PMC · DOI: 10.1093/nar/gkag107 · 2026-02-12

## TL;DR

This study reveals how HNRNPU, an RNA-binding protein, coordinates RNA metabolism and DNA methylation during brain development, linking it to neurodevelopmental disorders.

## Contribution

The study identifies HNRNPU's role in RNA regulation, chromatin remodeling, and DNA methylation, uncovering its molecular networks in neural differentiation.

## Key findings

- HNRNPU interacts with the SWI/SNF chromatin-remodeling complex and regulates translation.
- HNRNPU associates with mRNAs encoding proteins linked to neuronal development and neurodevelopmental disorders.
- Silencing HNRNPU alters DNA methylation at regulatory regions of neurodevelopmental transcription factors.

## Abstract

HNRNPU is an RNA-binding protein with diverse roles in transcriptional and post-transcriptional regulation. Pathogenic genetic variants of HNRNPU cause a severe neurodevelopmental disorder (NDD), but the underlying molecular mechanisms are unclear. Here, we comprehensively investigate the HNRNPU molecular interactome by integrating protein–protein interaction (PPI) mapping, RNA target identification, and genome-wide DNA methylation profiling in human neuroepithelial stem cells and differentiating neural cells. We identified extensive HNRNPU-centered networks, including an association with the mammalian SWI/SNF chromatin-remodeling complex, and uncovered a previously unrecognized role in translation. We present evidence that HNRNPU associates with messenger RNAs (mRNAs) encoding proteins important for neuronal development, including several linked to NDDs. Silencing HNRNPU reprogrammed methylation dynamics at regulatory regions, particularly at active and bivalent promoters of neurodevelopmental transcription factors. Integrative analysis across PPI, RNA, and methylome datasets identified 19 converging genes at all three molecular levels, including NDD genes within the SWI/SNF complex, SMARCA4 and SMARCC2, and RNA-processing machinery such as SYNCRIP. Together, these data showcase HNRNPU as a central coordinator of RNA metabolism and epigenetic remodeling during neural differentiation, linking RNA-binding, chromatin organization, and DNA methylation to the pathogenesis of HNRNPU-related NDDs.

Graphical Abstract

## Linked entities

- **Genes:** HNRNPU (heterogeneous nuclear ribonucleoprotein U) [NCBI Gene 3192], SMARCA4 (SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4) [NCBI Gene 6597], SMARCC2 (SWI/SNF related BAF chromatin remodeling complex subunit C2) [NCBI Gene 6601], SYNCRIP (synaptotagmin binding cytoplasmic RNA interacting protein) [NCBI Gene 10492]
- **Proteins:** HNRNPU (heterogeneous nuclear ribonucleoprotein U), SYNCRIP (synaptotagmin binding cytoplasmic RNA interacting protein)
- **Diseases:** neurodevelopmental disorder (MONDO:0700092)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** HNRNPU (heterogeneous nuclear ribonucleoprotein U) [NCBI Gene 3192] {aka DEE54, EIEE54, GRIP120, HNRNPU-AS1, HNRPU, SAF-A}, SMARCA4 (SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4) [NCBI Gene 6597] {aka BAF190, BAF190A, BRG1, CSS4, MRD16, OTSC12}, SMARCC2 (SWI/SNF related BAF chromatin remodeling complex subunit C2) [NCBI Gene 6601] {aka BAF170, CRACC2, CSS8, Rsc8}, SYNCRIP (synaptotagmin binding cytoplasmic RNA interacting protein) [NCBI Gene 10492] {aka GRY-RBP, GRYRBP, HNRNPQ, HNRPQ1, NSAP1, PP68}
- **Diseases:** NDD (MESH:D002658)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12895067/full.md

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Source: https://tomesphere.com/paper/PMC12895067