» Articles » PMID: 16508000

An Apparent Pseudo-exon Acts Both As an Alternative Exon That Leads to Nonsense-mediated Decay and As a Zero-length Exon

Overview
Journal Mol Cell Biol
Specialty Cell Biology
Date 2006 Mar 2
PMID 16508000
Citations 21
Authors
Affiliations
Soon will be listed here.
Abstract

Pseudo-exons are intronic sequences that are flanked by apparent consensus splice sites but that are not observed in spliced mRNAs. Pseudo-exons are often difficult to activate by mutation and have typically been viewed as a conceptual challenge to our understanding of how the spliceosome discriminates between authentic and cryptic splice sites. We have analyzed an apparent pseudo-exon located downstream of mutually exclusive exons 2 and 3 of the rat alpha-tropomyosin (TM) gene. The TM pseudo-exon is conserved among mammals and has a conserved profile of predicted splicing enhancers and silencers that is more typical of a genuine exon than a pseudo-exon. Splicing of the pseudo-exon is fully activated for splicing to exon 3 by a number of simple mutations. Splicing of the pseudo-exon to exon 3 is predicted to lead to nonsense-mediated decay (NMD). In contrast, when "prespliced" to exon 2 it follows a "zero length exon" splicing pathway in which a newly generated 5' splice site at the junction with exon 2 is spliced to exon 4. We propose that a subset of apparent pseudo-exons, as exemplified here, are actually authentic alternative exons whose inclusion leads to NMD.

Citing Articles

A single-cell strategy for the identification of intronic variants related to mis-splicing in pancreatic cancer.

Duman E, Sitte M, Conrads K, Mackay A, Ludewig F, Strobel P NAR Genom Bioinform. 2024; 6(2):lqae057.

PMID: 38800828 PMC: 11127633. DOI: 10.1093/nargab/lqae057.


Features of CFTR mRNA and implications for therapeutics development.

Jackson J, Mao Y, White Jr T, Foye C, Oliver K Front Genet. 2023; 14:1166529.

PMID: 37168508 PMC: 10165737. DOI: 10.3389/fgene.2023.1166529.


Genetic variants in S-adenosyl-methionine synthesis pathway and nonsyndromic cleft lip with or without cleft palate in Chile.

Salamanca C, Gonzalez-Hormazabal P, Recabarren A, Recabarren P, Pantoja R, Leiva N Pediatr Res. 2020; 89(4):1020-1025.

PMID: 32492698 DOI: 10.1038/s41390-020-0994-3.


Cutting a Long Intron Short: Recursive Splicing and Its Implications.

Georgomanolis T, Sofiadis K, Papantonis A Front Physiol. 2016; 7:598.

PMID: 27965595 PMC: 5126111. DOI: 10.3389/fphys.2016.00598.


Recursive splicing in long vertebrate genes.

Sibley C, Emmett W, Blazquez L, Faro A, Haberman N, Briese M Nature. 2015; 521(7552):371-375.

PMID: 25970246 PMC: 4471124. DOI: 10.1038/nature14466.


References
1.
Sun H, Chasin L . Multiple splicing defects in an intronic false exon. Mol Cell Biol. 2000; 20(17):6414-25. PMC: 86117. DOI: 10.1128/MCB.20.17.6414-6425.2000. View

2.
Han K, Yeo G, An P, Burge C, Grabowski P . A combinatorial code for splicing silencing: UAGG and GGGG motifs. PLoS Biol. 2005; 3(5):e158. PMC: 1079783. DOI: 10.1371/journal.pbio.0030158. View

3.
Wollerton M, Gooding C, Robinson F, Brown E, Jackson R, Smith C . Differential alternative splicing activity of isoforms of polypyrimidine tract binding protein (PTB). RNA. 2001; 7(6):819-32. PMC: 1370133. DOI: 10.1017/s1355838201010214. View

4.
Perez I, Lin C, McAfee J, Patton J . Mutation of PTB binding sites causes misregulation of alternative 3' splice site selection in vivo. RNA. 1997; 3(7):764-78. PMC: 1369523. View

5.
Gooding C, Roberts G, Moreau G, Nadal-Ginard B, Smith C . Smooth muscle-specific switching of alpha-tropomyosin mutually exclusive exon selection by specific inhibition of the strong default exon. EMBO J. 1994; 13(16):3861-72. PMC: 395299. DOI: 10.1002/j.1460-2075.1994.tb06697.x. View