» Articles » PMID: 16797197

General and Specific Functions of Exonic Splicing Silencers in Splicing Control

Overview
Journal Mol Cell
Publisher Cell Press
Specialty Cell Biology
Date 2006 Jun 27
PMID 16797197
Citations 107
Authors
Affiliations
Soon will be listed here.
Abstract

Correct splice site recognition is critical in pre-mRNA splicing. We find that almost all of a diverse panel of exonic splicing silencer (ESS) elements alter splice site choice when placed between competing sites, consistently inhibiting use of intron-proximal 5' and 3' splice sites. Supporting a general role for ESSs in splice site definition, we found that ESSs are both abundant and highly conserved between alternative splice site pairs and that mutation of ESSs located between natural alternative splice site pairs consistently shifted splicing toward the intron-proximal site. Some exonic splicing enhancers (ESEs) promoted use of intron-proximal 5' splice sites, and tethering of hnRNP A1 and SF2/ASF proteins between competing splice sites mimicked the effects of ESS and ESE elements, respectively. Further, we observed that specific subsets of ESSs had distinct effects on a multifunctional intron retention reporter and that one of these subsets is likely preferred for regulation of endogenous intron retention events. Together, our findings provide a comprehensive picture of the functions of ESSs in the control of diverse types of splicing decisions.

Citing Articles

The Intricate Functional Networks of Pre-mRNA Alternative Splicing in Mammalian Spermatogenesis.

Jiang N, Li Y, Yin L, Yuan S, Wang F Int J Mol Sci. 2024; 25(22).

PMID: 39596142 PMC: 11594017. DOI: 10.3390/ijms252212074.


Investigating the influence of the SIRT6 gene and alternative splicing on canine longevity: an in-depth bioinformatics analysis and experimental confirmation via NGS-based targeted sequencing.

Ozmen O, Koklu G Geroscience. 2024; .

PMID: 39433703 DOI: 10.1007/s11357-024-01386-8.


From computational models of the splicing code to regulatory mechanisms and therapeutic implications.

Capitanchik C, Wilkins O, Wagner N, Gagneur J, Ule J Nat Rev Genet. 2024; 26(3):171-190.

PMID: 39358547 DOI: 10.1038/s41576-024-00774-2.


Genetic constraints in genes exhibiting splicing plasticity in facultative diapause.

Steward R, Pruisscher P, Roberts K, Wheat C Heredity (Edinb). 2024; 132(3):142-155.

PMID: 38291272 PMC: 10923799. DOI: 10.1038/s41437-024-00669-2.


Identification of Significant RNA-Binding Proteins in the Process of CD44 Splicing Using the Boosted Beta Regression Algorithm.

Novosad V Dokl Biochem Biophys. 2023; 510(1):99-103.

PMID: 37582871 DOI: 10.1134/S1607672923700199.


References
1.
Fairbrother W, Holste D, Burge C, Sharp P . Single nucleotide polymorphism-based validation of exonic splicing enhancers. PLoS Biol. 2004; 2(9):E268. PMC: 514884. DOI: 10.1371/journal.pbio.0020268. View

2.
Yeo G, Burge C . Maximum entropy modeling of short sequence motifs with applications to RNA splicing signals. J Comput Biol. 2004; 11(2-3):377-94. DOI: 10.1089/1066527041410418. View

3.
Nagoshi R, McKeown M, Burtis K, Belote J, Baker B . The control of alternative splicing at genes regulating sexual differentiation in D. melanogaster. Cell. 1988; 53(2):229-36. DOI: 10.1016/0092-8674(88)90384-4. View

4.
Ge H, Manley J . A protein factor, ASF, controls cell-specific alternative splicing of SV40 early pre-mRNA in vitro. Cell. 1990; 62(1):25-34. DOI: 10.1016/0092-8674(90)90236-8. View

5.
Krainer A, Conway G, Kozak D . The essential pre-mRNA splicing factor SF2 influences 5' splice site selection by activating proximal sites. Cell. 1990; 62(1):35-42. DOI: 10.1016/0092-8674(90)90237-9. View