Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow Print PDF (225K) Freely available
Right arrow Supplementary Material
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (61)
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Roca, X.
Right arrow Articles by Krainer, A. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Roca, X.
Right arrow Articles by Krainer, A. R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 2003, Vol. 31, No. 21 6321-6333
© 2003 Oxford University Press

Intrinsic differences between authentic and cryptic 5' splice sites

Xavier Roca, Ravi Sachidanandam and Adrian R. Krainer*

Cold Spring Harbor Laboratory, PO Box 100, Cold Spring Harbor, NY 11724, USA

*To whom correspondence should be addressed. Tel: +1 516 367 8417; Fax: +1 516 367 8815; Email: krainer{at}cshl.edu

Cryptic splice sites are used only when use of a natural splice site is disrupted by mutation. To determine the features that distinguish authentic from cryptic 5' splice sites (5'ss), we systematically analyzed a set of 76 cryptic 5'ss derived from 46 human genes. These cryptic 5'ss have a similar frequency distribution in exons and introns, and are usually located close to the authentic 5'ss. Statistical analysis of the strengths of the 5'ss using the Shapiro and Senapathy matrix revealed that authentic 5'ss have significantly higher score values than cryptic 5'ss, which in turn have higher values than the mutant ones. ß-Globin provides an interesting exception to this rule, so we chose it for detailed experimental analysis in vitro. We found that the sequences of the ß-globin authentic and cryptic 5'ss, but not their surrounding context, determine the correct 5'ss choice, although their respective scores do not reflect this functional difference. Our analysis provides a statistical basis to explain the competitive advantage of authentic over cryptic 5'ss in most cases, and should facilitate the development of tools to reliably predict the effect of disease-associated 5'ss-disrupting mutations at the mRNA level.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Med. Genet.Home page
Y Habara, Y Takeshima, H Awano, Y Okizuka, Z Zhang, K Saiki, M Yagi, and M Matsuo
In vitro splicing analysis showed that availability of a cryptic splice site is not a determinant for alternative splicing patterns caused by +1G->A mutations in introns of the dystrophin gene
J. Med. Genet., August 1, 2009; 46(8): 542 - 547.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
M. Dassah, S. Patzek, V. M. Hunt, P. E. Medina, and A. M. Zahler
A Genetic Screen for Suppressors of a Mutated 5' Splice Site Identifies Factors Associated With Later Steps of Spliceosome Assembly
Genetics, July 1, 2009; 182(3): 725 - 734.
[Abstract] [Full Text] [PDF]


Home page
CJASNHome page
K. Wang, X. Zhao, S. Chan, O. Cil, N. He, X. Song, A. D. Paterson, and Y. Pei
Evidence for Pathogenicity of Atypical Splice Mutations in Autosomal Dominant Polycystic Kidney Disease
Clin. J. Am. Soc. Nephrol., February 1, 2009; 4(2): 442 - 449.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
O. Ram, S. Schwartz, and G. Ast
Multifactorial Interplay Controls the Splicing Profile of Alu-Derived Exons
Mol. Cell. Biol., May 15, 2008; 28(10): 3513 - 3525.
[Abstract] [Full Text] [PDF]


Home page
Genome ResHome page
X. Roca, A. J. Olson, A. R. Rao, E. Enerly, V. N. Kristensen, A.-L. Borresen-Dale, B. S. Andresen, A. R. Krainer, and R. Sachidanandam
Features of 5'-splice-site efficiency derived from disease-causing mutations and comparative genomics
Genome Res., January 1, 2008; 18(1): 77 - 87.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
J. Kralovicova and I. Vorechovsky
Global control of aberrant splice-site activation by auxiliary splicing sequences: evidence for a gradient in exon and intron definition
Nucleic Acids Res., October 8, 2007; 35(19): 6399 - 6413.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
E. Buratti, M. Chivers, J. Kralovicova, M. Romano, M. Baralle, A. R. Krainer, and I. Vorechovsky
Aberrant 5' splice sites in human disease genes: mutation pattern, nucleotide structure and comparison of computational tools that predict their utilization
Nucleic Acids Res., July 26, 2007; 35(13): 4250 - 4263.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
I. Vorechovsky
Aberrant 3' splice sites in human disease genes: mutation pattern, nucleotide structure and comparison of computational tools that predict their utilization
Nucleic Acids Res., September 15, 2006; (2006) gkl535v2.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
N. Sheth, X. Roca, M. L. Hastings, T. Roeder, A. R. Krainer, and R. Sachidanandam
Comprehensive splice-site analysis using comparative genomics
Nucleic Acids Res., September 1, 2006; 34(14): 3955 - 3967.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
E. Buratti, M. Baralle, and F. E. Baralle
Defective splicing, disease and therapy: searching for master checkpoints in exon definition
Nucleic Acids Res., July 19, 2006; 34(12): 3494 - 3510.
[Abstract] [Full Text] [PDF]


Home page
RNAHome page
S. Spena, M. L. Tenchini, and E. Buratti
Cryptic splice site usage in exon 7 of the human fibrinogen B{beta}-chain gene is regulated by a naturally silent SF2/ASF binding site within this exon
RNA, June 1, 2006; 12(6): 948 - 958.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
A. W. Hart, L. McKie, J. E. Morgan, P. Gautier, K. West, I. J. Jackson, and S. H. Cross
Genotype-Phenotype Correlation of Mouse Pde6b Mutations
Invest. Ophthalmol. Vis. Sci., September 1, 2005; 46(9): 3443 - 3450.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
J. Kralovicova, M. B. Christensen, and I. Vorechovsky
Biased exon/intron distribution of cryptic and de novo 3' splice sites
Nucleic Acids Res., September 1, 2005; 33(15): 4882 - 4898.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
H. Lei, I. N. M. Day, and I. Vorechovsky
Exonization of AluYa5 in the human ACE gene requires mutations in both 3' and 5' splice sites and is facilitated by a conserved splicing enhancer
Nucleic Acids Res., July 14, 2005; 33(12): 3897 - 3906.
[Abstract] [Full Text] [PDF]


Home page
RNAHome page
X. ROCA, R. SACHIDANANDAM, and A. R. KRAINER
Determinants of the inherent strength of human 5' splice sites
RNA, May 1, 2005; 11(5): 683 - 698.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
R. Colobran, P. Adreani, Y. Ashhab, A. Llano, J. A. Este, O. Dominguez, R. Pujol-Borrell, and M. Juan
Multiple Products Derived from Two CCL4 Loci: High Incidence of a New Polymorphism in HIV+ Patients
J. Immunol., May 1, 2005; 174(9): 5655 - 5664.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
E. Buratti, M. Baralle, L. De Conti, D. Baralle, M. Romano, Y. M. Ayala, and F. E. Baralle
hnRNP H binding at the 5' splice site correlates with the pathological effect of two intronic mutations in the NF-1 and TSH{beta} genes
Nucleic Acids Res., August 6, 2004; 32(14): 4224 - 4236.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
A. M. Zahler, J. D. Tuttle, and A. D. Chisholm
Genetic Suppression of Intronic +1G Mutations by Compensatory U1 snRNA Changes in Caenorhabditis elegans
Genetics, August 1, 2004; 167(4): 1689 - 1696.
[Abstract] [Full Text] [PDF]


Home page
J. Med. Genet.Home page
R Kan, S R F Twigg, J Berg, L Wang, F Jin, and A O M Wilkie
Expression analysis of an FGFR2 IIIc 5' splice site mutation (1084+3A->G)
J. Med. Genet., August 1, 2004; 41(8): e108 - e108.
[Full Text] [PDF]


Home page
Nucleic Acids ResHome page
M. Zeniou, R. Gattoni, A. Hanauer, and J. Stevenin
Delineation of the mechanisms of aberrant splicing caused by two unusual intronic mutations in the RSK2 gene involved in Coffin-Lowry syndrome
Nucleic Acids Res., February 18, 2004; 32(3): 1214 - 1223.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.