# NRDE2 Interacts with an Early Transcription Elongation Complex and Widely Impacts Gene Expression

**Authors:** Marina Srbic, Chaïmaa Belhaouari, Raoul Raffel, Laurine Lemaire, Jerome Barbier, Julie Bossuyt, Charbel Akkawi, Xavier Contreras, Rosemary Kiernan

PMC · DOI: 10.3390/ijms26199792 · 2025-10-08

## TL;DR

NRDE2 interacts with transcription and splicing complexes in human cells and affects gene expression on a large scale.

## Contribution

NRDE2's interaction with transcription elongation complexes and its broader impact on RNA processing are newly identified.

## Key findings

- NRDE2 interacts with chromatin-associated transcription factors like the PAF1 complex and elongating RNA polymerase II.
- Depletion of NRDE2 leads to widespread changes in gene expression and increased intron retention.
- Intron retention caused by NRDE2 loss is often linked to reduced mRNA levels.

## Abstract

NRDE2 is a highly conserved protein implicated in post-transcriptional gene silencing in Schizosaccharomyces pombe and Caenorhabditis elegans and has been shown to modulate splicing in mammals. To explore whether NRDE2 participates in additional processes in human cells, we performed tandem affinity purification followed by proteomic analysis of NRDE2 from nuclear extracts of HEK293T and HeLa cells. Our analysis confirmed the interaction of NRDE2 with its well-characterized partner, the MTR4 helicase (MTREX), as well as with multiple splicing factors. Notably, we also identified interactions with chromatin-associated proteins involved in transcription, including the Polymerase-Associated Factor 1 (PAF1) complex and elongating forms of RNA polymerase II (RNAPII). To further investigate NRDE2 function, we conducted RNA-seq following its transient depletion. Differential expression analysis revealed that loss of NRDE2 alters the expression of thousands of genes. Consistent with earlier reports, we observed splicing defects, particularly intron retention; however, our results indicate that the impact of NRDE2 on intron retention is more extensive than previously recognized. Moreover, intron retention was frequently associated with reduced mRNA expression. Together, these findings suggest that NRDE2 associates with both transcriptional and splicing machineries and plays a broader role in RNA processing than previously appreciated.

## Linked entities

- **Genes:** NRDE2 (NRDE-2, necessary for RNA interference, domain containing) [NCBI Gene 55051], MTREX (Mtr4 exosome RNA helicase) [NCBI Gene 23517], PAF1 (PAF1 component of Paf1/RNA polymerase II complex) [NCBI Gene 54623], RNA polymerase II (DNA-directed RNA polymerase II subunit RPB7) [NCBI Gene 547985]
- **Proteins:** NRDE2 (NRDE-2, necessary for RNA interference, domain containing)
- **Species:** Schizosaccharomyces pombe (taxon 4896), Caenorhabditis elegans (taxon 6239), Homo sapiens (taxon 9606), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** PAF1 (PAF1 component of Paf1/RNA polymerase II complex) [NCBI Gene 54623] {aka F23149_1, PD2}, NRDE2 (NRDE-2, necessary for RNA interference, domain containing) [NCBI Gene 55051] {aka C14orf102}
- **Species:** Homo sapiens (human, species) [taxon 9606], Caenorhabditis elegans (species) [taxon 6239]
- **Cell lines:** HEK293T — Homo sapiens (Human), Transformed cell line (CVCL_0063), HeLa — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_0030)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12524662/full.md

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Source: https://tomesphere.com/paper/PMC12524662