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Updated: Jul 7, 2025

A Reporter Based Cellular Assay for Monitoring Splicing Efficiency
Published on: September 15, 2021
CCAR-1 works together with the U2AF large subunit UAF-1 to regulate alternative splicing
Doreen I Lugano, Lindsey N Barrett, Dale Chaput
1Department of Cell Biology, Microbiology, and Molecular Biology, University of South Florida, Tampa, FL, USA.
Abstract:
The Cell Division Cycle and Apoptosis Regulator (CCAR) protein family members have recently emerged as regulators of alternative splicing and transcription, as well as having other key physiological functions. For example, mammalian CCAR2/DBC1 forms a complex with the zinc factor protein ZNF326 to integrate alternative splicing with RNA polymerase II transcriptional elongation in AT-rich regions of the DNA. Additionally, Caenorhabditis elegans CCAR-1, a homolog to mammalian CCAR2, facilitates the alternative splicing of the perlecan unc-52 gene. However, much about the CCAR family's role in alternative splicing is unknown. Here, we have examined the role of CCAR-1 in genome-wide alternative splicing in Caenorhabditis elegans and have identified new alternative splicing targets of CCAR-1 using RNA sequencing. Also, we found that CCAR-1 interacts with the spliceosome factors UAF-1 and UAF-2 using mass spectrometry, and that knockdown of ccar-1 affects alternative splicing patterns, motility, and proteostasis of UAF-1 mutant worms. Collectively, we demonstrate the role of CCAR-1 in regulating global alternative splicing in C. elegans and in conjunction with UAF-1.
Insights
Cell Division Cycle and Apoptosis Regulator-1 (CCAR-1) globally regulates alternative splicing in C. elegans. This study identifies new CCAR-1 targets and its interaction with spliceosome factors, impacting worm motility and proteostasis.
Area of Science:
- Molecular Biology
- Genetics
- Developmental Biology
Background:
- Cell Division Cycle and Apoptosis Regulator (CCAR) proteins are emerging regulators of gene expression.
- CCAR proteins influence alternative splicing and transcription, impacting key physiological functions.
- Mammalian CCAR2/DBC1 integrates splicing with transcription, while C. elegans CCAR-1 affects the unc-52 gene.
Purpose of the Study:
- To investigate the genome-wide role of CCAR-1 in alternative splicing in C. elegans.
- To identify novel CCAR-1-regulated alternative splicing targets.
- To elucidate the functional interactions of CCAR-1 with spliceosome components.
Main Methods:
- RNA sequencing to identify genome-wide alternative splicing targets.
- Mass spectrometry to determine protein-protein interactions.
- Gene knockdown experiments in C. elegans.
Main Results:
- CCAR-1 regulates global alternative splicing patterns in C. elegans.
- New alternative splicing targets of CCAR-1 were identified.
- CCAR-1 interacts with spliceosome factors UAF-1 and UAF-2.
- Knockdown of ccar-1 impacts alternative splicing, motility, and proteostasis in UAF-1 mutant worms.
Conclusions:
- CCAR-1 is a key regulator of global alternative splicing in C. elegans.
- CCAR-1 functions in conjunction with spliceosome factor UAF-1.
- These findings expand our understanding of CCAR family functions in gene regulation.
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