Literature DB >> 9367866

Six novel transcripts that remove a huge intron ranging from 250 to 800 kb are produced by alternative splicing of the 5' region of the dystrophin gene in human skeletal muscle.

A Surono1, Y Takeshima, T Wibawa, Z A Pramono, M Matsuo.   

Abstract

The dystrophin gene, which is mutated in patients with Duchenne and Becker muscular dystrophies, comprises 79 exons and is thus the largest known human gene. A full spectrum of splicing of dystrophin transcript has not been elucidated yet. In this study, 6 novel alternative splicing reactions were discovered in the 5' region by amplifying the cDNA corresponding to exons M1 through 18. Two of these novel transcripts maintain the translational reading frame and are presumed to produce truncated dystrophin, while the other four have disrupted reading frames. The physical distance between splice donor and acceptor sites ranged from 250 kb to 800 kb. Furthermore, the same six alternative splicing products were obtained from mouse skeletal muscle cDNA. This indicated that these novel alternative splicing events are conserved in humans and mice.

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Year:  1997        PMID: 9367866     DOI: 10.1006/bbrc.1997.7579

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  7 in total

1.  Identification of seven novel cryptic exons embedded in the dystrophin gene and characterization of 14 cryptic dystrophin exons.

Authors:  Zhujun Zhang; Yasuaki Habara; Atsushi Nishiyama; Yoshinobu Oyazato; Mariko Yagi; Yasuhiro Takeshima; Masafumi Matsuo
Journal:  J Hum Genet       Date:  2007-06-20       Impact factor: 3.172

2.  Neuronal SH-SY5Y cells use the C-dystrophin promoter coupled with exon 78 skipping and display multiple patterns of alternative splicing including two intronic insertion events.

Authors:  Atsushi Nishida; Maki Minegishi; Atsuko Takeuchi; Hiroyuki Awano; Emma Tabe Eko Niba; Masafumi Matsuo
Journal:  Hum Genet       Date:  2015-07-08       Impact factor: 4.132

3.  A novel cryptic exon identified in the 3' region of intron 2 of the human dystrophin gene.

Authors:  Van Khanh Tran; Zhujun Zhang; Mariko Yagi; Atsushi Nishiyama; Yasuaki Habara; Yasuhiro Takeshima; Masafumi Matsuo
Journal:  J Hum Genet       Date:  2005-08-30       Impact factor: 3.172

Review 4.  Normal and altered pre-mRNA processing in the DMD gene.

Authors:  Sylvie Tuffery-Giraud; Julie Miro; Michel Koenig; Mireille Claustres
Journal:  Hum Genet       Date:  2017-06-09       Impact factor: 4.132

5.  Comparative analysis of vertebrate dystrophin loci indicate intron gigantism as a common feature.

Authors:  Uberto Pozzoli; Greg Elgar; Rachele Cagliani; Laura Riva; Giacomo P Comi; Nereo Bresolin; Alessandra Bardoni; Manuela Sironi
Journal:  Genome Res       Date:  2003-05       Impact factor: 9.043

6.  Targeted RNA-Seq profiling of splicing pattern in the DMD gene: exons are mostly constitutively spliced in human skeletal muscle.

Authors:  Anne-Laure Bougé; Eva Murauer; Emmanuelle Beyne; Julie Miro; Jessica Varilh; Magali Taulan; Michel Koenig; Mireille Claustres; Sylvie Tuffery-Giraud
Journal:  Sci Rep       Date:  2017-01-03       Impact factor: 4.379

7.  Dp412e: a novel human embryonic dystrophin isoform induced by BMP4 in early differentiated cells.

Authors:  Emmanuelle Massouridès; Jérôme Polentes; Philippe-Emmanuel Mangeot; Virginie Mournetas; Juliette Nectoux; Nathalie Deburgrave; Patrick Nusbaum; France Leturcq; Linda Popplewell; George Dickson; Nicolas Wein; Kevin M Flanigan; Marc Peschanski; Jamel Chelly; Christian Pinset
Journal:  Skelet Muscle       Date:  2015-11-14       Impact factor: 4.912

  7 in total

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