Literature DB >> 17295913

Functional analysis of splicing mutations in exon 7 of NF1 gene.

Irene Bottillo1, Alessandro De Luca, Annalisa Schirinzi, Valentina Guida, Isabella Torrente, Stefano Calvieri, Cristina Gervasini, Lidia Larizza, Antonio Pizzuti, Bruno Dallapiccola.   

Abstract

BACKGROUND: Neurofibromatosis type 1 is one of the most common autosomal dominant disorders, affecting about 1:3,500 individuals. NF1 exon 7 displays weakly defined exon-intron boundaries, and is particularly prone to missplicing.
METHODS: In this study we investigated the expression of exon 7 transcripts using bioinformatic identification of splicing regulatory sequences, and functional minigene analysis of four sequence changes [c.910C>T (R304X), c.945G>A/c.946C>A (Q315Q/L316M), c.1005T>C (N335N)] identified in exon 7 of three different NF1 patients.
RESULTS: Our results detected the presence of three exonic splicing enhancers (ESEs) and one putative exonic splicing silencer (ESS) element. The wild type minigene assay resulted in three alternative isoforms, including a transcript lacking NF1 exon 7 (NF1DeltaE7). Both the wild type and the mutated constructs shared NF1DeltaE7 in addition to the complete messenger, but displayed a different ratio between the two transcripts. In the presence of R304X and Q315Q/L316M mutations, the relative proportion between the different isoforms is shifted toward the expression of NF1DeltaE7, while in the presence of N335N variant, the NF1DeltaE7 expression is abolished.
CONCLUSION: In conclusion, it appears mandatory to investigate the role of each nucleotide change within the NF1 coding sequence, since a significant proportion of NF1 exon 7 mutations affects pre-mRNA splicing, by disrupting exonic splicing motifs and modifying the delicate balance between aberrantly and correctly spliced transcripts.

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Year:  2007        PMID: 17295913      PMCID: PMC1802069          DOI: 10.1186/1471-2350-8-4

Source DB:  PubMed          Journal:  BMC Med Genet        ISSN: 1471-2350            Impact factor:   2.103


  35 in total

1.  Quantification of splice variants using real-time PCR.

Authors:  I I Vandenbroucke; J Vandesompele; A D Paepe; L Messiaen
Journal:  Nucleic Acids Res       Date:  2001-07-01       Impact factor: 16.971

Review 2.  Listening to silence and understanding nonsense: exonic mutations that affect splicing.

Authors:  Luca Cartegni; Shern L Chew; Adrian R Krainer
Journal:  Nat Rev Genet       Date:  2002-04       Impact factor: 53.242

3.  Cold shock induces the insertion of a cryptic exon in the neurofibromatosis type 1 (NF1) mRNA.

Authors:  E Ars; E Serra; S de la Luna; X Estivill; C Lázaro
Journal:  Nucleic Acids Res       Date:  2000-03-15       Impact factor: 16.971

4.  Three different premature stop codons lead to skipping of exon 7 in neurofibromatosis type I patients.

Authors:  K Wimmer; M Eckart; P F Stadler; H Rehder; C Fonatsch
Journal:  Hum Mutat       Date:  2000-07       Impact factor: 4.878

5.  NF1 mutation rather than individual genetic variability is the main determinant of the NF1-transcriptional profile of mutations affecting splicing.

Authors:  Eva Pros; Sara Larriba; Eva López; Anna Ravella; M Lluïsa Gili; Helena Kruyer; Joan Valls; Eduard Serra; Conxi Lázaro
Journal:  Hum Mutat       Date:  2006-11       Impact factor: 4.878

6.  Illegitimate splicing of the NF1 gene in healthy individuals mimics mutation-induced splicing alterations in NF1 patients.

Authors:  K Wimmer; M Eckart; H Rehder; C Fonatsch
Journal:  Hum Genet       Date:  2000-03       Impact factor: 4.132

7.  Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects.

Authors:  L M Messiaen; T Callens; G Mortier; D Beysen; I Vandenbroucke; N Van Roy; F Speleman; A D Paepe
Journal:  Hum Mutat       Date:  2000       Impact factor: 4.878

8.  Quantification of NF1 transcripts reveals novel highly expressed splice variants.

Authors:  Ina Vandenbroucke; Jo Vandesompele; Anne De Paepe; Ludwine Messiaen
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9.  The N-terminal splice product NF1-10a-2 of the NF1 gene codes for a transmembrane segment.

Authors:  Dieter Kaufmann; Ralf Müller; Oliver Kenner; Werner Leistner; Christian Hein; Walther Vogel; Britta Bartelt
Journal:  Biochem Biophys Res Commun       Date:  2002-06-07       Impact factor: 3.575

10.  Ten novel mutations in the human neurofibromatosis type 1 (NF1) gene in Italian patients.

Authors:  Paola Origone; Alessandro De Luca; Carlo Bellini; Anna Buccino; Rita Mingarelli; Simona Costabel; Carmen La Rosa; Cecilia Garrè; Domenico A Coviello; Franco Ajmar; Bruno Dallapiccola; Eugenio Bonioli
Journal:  Hum Mutat       Date:  2002-07       Impact factor: 4.878

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5.  The contribution of GPR98 and DFNB31 genes to a Spanish Usher syndrome type 2 cohort.

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6.  Study of USH1 splicing variants through minigenes and transcript analysis from nasal epithelial cells.

Authors:  María José Aparisi; Gema García-García; Elena Aller; María Dolores Sequedo; Cristina Martínez-Fernández de la Cámara; Regina Rodrigo; Miguel Armengot; Julio Cortijo; Javier Milara; Manuel Díaz-LLopis; Teresa Jaijo; José María Millán
Journal:  PLoS One       Date:  2013-02-25       Impact factor: 3.240

7.  Functional Analysis of Mutations in Exon 9 of NF1 Reveals the Presence of Several Elements Regulating Splicing.

Authors:  Elisabete Hernández-Imaz; Yolanda Martín; Laura de Conti; German Melean; Ana Valero; Marco Baralle; Concepción Hernández-Chico
Journal:  PLoS One       Date:  2015-10-28       Impact factor: 3.240

8.  A recurrent deletion in the SLC5A2 gene including the intron 7 branch site responsible for familial renal glucosuria.

Authors:  Xiangzhong Zhao; Li Cui; Yanhua Lang; Ting Liu; Jingru Lu; Cui Wang; Sylvie Tuffery-Giraud; Irene Bottillo; Xinsheng Wang; Leping Shao
Journal:  Sci Rep       Date:  2016-09-26       Impact factor: 4.379

9.  The Study of a 231 French Patient Cohort Significantly Extends the Mutational Spectrum of the Two Major Usher Genes MYO7A and USH2A.

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  9 in total

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