Previous Article | Next Article 
Mol Cell Biol. 1987 September; 7(9): 3194-3198
Amount of RNA secondary structure required to induce an alternative splice.
D Solnick and
S I Lee
Department of Molecular Biophysics and Biochemistry, Yale University School of Medicine, New Haven, Connecticut 06510.
ABSTRACT
We set up an alternative splicing system in vitro in which the relative amounts of two spliced RNAs, one containing and the other lacking a particular exon, were directly proportional to the length of an inverted repeat inserted into the flanking introns. We then used the system to measure the effect of intramolecular complementarity on alternative splicing in vivo. We found that an alternative splice was induced in vivo only when the introns contained more than approximately 50 nucleotides of perfect complementarity, that is, only when the secondary structure was much more stable than most if not all possible secondary structures in natural mRNA precursors. We showed further that intron insertions containing long complements to splice sites and a branch point inhibited splicing in vitro but not in vivo. These results raise the possibility that in cells most pre-mRNA secondary structures either are not maintained long enough to influence splicing choices, or never form at all.
Mol Cell Biol. 1987 September; 7(9): 3194-3198
This article has been cited by other articles:
-
Lian, Y., Garner, H. R.
(2005). Evidence for the regulation of alternative splicing via complementary DNA sequence repeats. Bioinformatics
21: 1358-1364
[Abstract]
[Full Text]
-
Buratti, E., Baralle, F. E.
(2004). Influence of RNA Secondary Structure on the Pre-mRNA Splicing Process. Mol. Cell. Biol.
24: 10505-10514
[Full Text]
-
Flomen, R., Knight, J., Sham, P., Kerwin, R., Makoff, A.
(2004). Evidence that RNA editing modulates splice site selection in the 5-HT2C receptor gene. Nucleic Acids Res
32: 2113-2122
[Abstract]
[Full Text]
-
Attanasio, C., David, A., Neerman-Arbez, M.
(2003). Outcome of donor splice site mutations accounting for congenital afibrinogenemia reflects order of intron removal in the fibrinogen alpha gene (FGA). Blood
101: 1851-1856
[Abstract]
[Full Text]
-
Muh, S. J., Hovhannisyan, R. H., Carstens, R. P.
(2002). A Non-sequence-specific Double-stranded RNA Structural Element Regulates Splicing of Two Mutually Exclusive Exons of Fibroblast Growth Factor Receptor 2 (FGFR2). J. Biol. Chem.
277: 50143-50154
[Abstract]
[Full Text]
-
Jiang, Z., Cote, J., Kwon, J. M., Goate, A. M., Wu, J. Y.
(2000). Aberrant Splicing of tau Pre-mRNA Caused by Intronic Mutations Associated with the Inherited Dementia Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17. Mol. Cell. Biol.
20: 4036-4048
[Abstract]
[Full Text]
-
Kosaki, A., Nelson, J., Webster, N. J. G.
(1998). Identification of Intron and Exon Sequences Involved in Alternative Splicing of Insulin Receptor Pre-mRNA. J. Biol. Chem.
273: 10331-10337
[Abstract]
[Full Text]
-
Vilardell, J, Warner, J R
(1994). Regulation of splicing at an intermediate step in the formation of the spliceosome.. Genes Dev.
8: 211-220
[Abstract]
-
Watakabe, A, Tanaka, K, Shimura, Y
(1993). The role of exon sequences in splice site selection.. Genes Dev.
7: 407-418
[Abstract]
-
Clouet d'Orval, B, d'Aubenton Carafa, Y, Sirand-Pugnet, P, Gallego, M, Brody, E, Marie, J
(1991). RNA secondary structure repression of a muscle-specific exon in HeLa cell nuclear extracts. Science
252: 1823-1828
[Abstract]
-
Libri, D, Piseri, A, Fiszman, M.
(1991). Tissue-specific splicing in vivo of the beta-tropomyosin gene: dependence on an RNA secondary structure. Science
252: 1842-1845
[Abstract]
-
Nasim, F H, Spears, P A, Hoffmann, H M, Kuo, H C, Grabowski, P J
(1990). A Sequential splicing mechanism promotes selection of an optimal exon by repositioning a downstream 5' splice site in preprotachykinin pre-mRNA.. Genes Dev.
4: 1172-1184
[Abstract]
-
Beyer, A L, Osheim, Y N
(1988). Splice site selection, rate of splicing, and alternative splicing on nascent transcripts.. Genes Dev.
2: 754-765
[Abstract]
Copyright © 1987 by the American Society for Microbiology. All rights reserved.