Journal Article

CELF1 Downregulation Promotes Cardiomyocyte Hypertrophy via Regulating Alternative Splicing of Tead1

Liu, Yiqiao, Zhu, Kaili, Zeng, Siying, Zhang, Shengqi, Ni, Le, Hu, Lingjie

2026

Overview

Background/Objectives: The RNA-binding protein CELF1 is crucial for cardiac development, but its role in cardiomyocyte hypertrophy is unclear. This study investigates the effects of acute CELF1 knockdown on alternative splicing and hypertrophic growth in cardiomyocytes. Methods: Neonatal rat cardiomyocytes (NRCMs) were transfected with two siRNAs targeting CELF1. Hypertrophy was assessed by cell size and expression of hypertrophic markers via qPCR and Western blot. RNA sequencing was performed in NRCMs to identify alternative splicing events. Tead1 function was tested by knockdown in NRCMs. Selected mechanistic assays were performed primarily in HeLa cells. Results: CELF1 knockdown in NRCMs increased cardiomyocyte size and upregulated hypertrophic markers, while its overexpression restored the phenotype. RNA-seq revealed that CELF1 knockdown alters the alternative splicing pattern. Specifically, the splicing of the transcription factor Tead1 shifted from the full-length long Tead1 isoform (Tead1-L) to the exon 4-skipped short isoform (Tead1-S). In HeLa cells, CELF1 interacted with hnRNPC, an m6A reader and splicing factor, and CELF1 perturbation correlated with changes in global m6A abundance. Conclusions: These findings suggest that CELF1 regulates hypertrophic phenotypes in cardiomyocytes and is associated with alternative splicing of Tead1.

• Publisher: MDPI AG,Multidisciplinary Digital Publishing Institute (MDPI)
• Subject: Alternative splicing / Alternative Splicing - genetics / Animals / Cardiomegaly - genetics / Cardiomegaly - metabolism / Cardiomegaly - pathology / Cardiomyocytes / CELF1 Protein - genetics / CELF1 Protein - metabolism / Cell size / Cloning / DNA-Binding Proteins - genetics / DNA-Binding Proteins - metabolism / Down-Regulation / Ethylenediaminetetraacetic acid / Experiments / Heart failure / HeLa Cells / Humans / Hypertrophy / Myocytes, Cardiac - metabolism / Myocytes, Cardiac - pathology / Neonates / Phenotypes / Plasmids / Protein binding / Proteins / Quantitative analysis / Rats / Rats, Sprague-Dawley / Reagents / RNA / RNA sequencing / RNA-binding protein / siRNA / Splicing factors / TEA Domain Transcription Factors - genetics / Transcription Factors - genetics / Transcription Factors - metabolism