Literature DB >> 9446807

The 5' region of intron 11 of the dystrophin gene contains target sequences for mobile elements and three overlapping ORFs.

A Ferlini1, F Muntoni.   

Abstract

We have characterised the 2371 bp 5' end of intron 11 of the dystrophin gene. Comparative analysis of this intronic region revealed homologies with the following sequences: regions containing mobile elements; target sites for numerous transcription factors, two resolvases, and a histone-like DNA binding protein; three eukaryotic promoters. In addition, we identified three partially overlapping ORFs, and transcription analysis confirmed that one of these is expressed, representing the first gene reported to overlap the human dystrophin gene. We have also characterised a 136 bp sequence rearranged in intron 11 in a patient affected by X-linked dilated cardiomyopathy due to a dystrophinopathy. This is a multiple copy sequence with features of a repetitive element. Its comparative analysis showed a very high homology with human genomic and EST regions, adjacent and clustered with Alu, LINE1, and THE elements. The pattern of homology suggests that it may represent a novel Alu-like, transcriptionally active sequence with a possible retrotransposable capacity. We hypothesise that the 5' region of the dystrophin intron 11, containing common target areas for the insertion of mobile elements, may have a role in the rearrangement of this novel Alu-like sequence.

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Year:  1998        PMID: 9446807     DOI: 10.1006/bbrc.1997.7976

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


  11 in total

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Journal:  Cytotechnology       Date:  2007-02-28       Impact factor: 2.058

2.  A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathy.

Authors:  A Ferlini; N Galié; L Merlini; C Sewry; A Branzi; F Muntoni
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

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

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Journal:  J Hum Genet       Date:  2005-08-30       Impact factor: 3.172

4.  Microarray-based mutation detection in the dystrophin gene.

Authors:  Madhuri R Hegde; Ephrem L H Chin; Jennifer G Mulle; David T Okou; Stephen T Warren; Michael E Zwick
Journal:  Hum Mutat       Date:  2008-09       Impact factor: 4.878

5.  Exon skipping caused by an intronic insertion of a young Alu Yb9 element leads to severe hemophilia A.

Authors:  Arupa Ganguly; Tanya Dunbar; Peiqin Chen; Lynn Godmilow; Tapan Ganguly
Journal:  Hum Genet       Date:  2003-07-12       Impact factor: 4.132

6.  Tempo and mode of evolution of a primate-specific retrotransposon belonging to the LINE 1 family.

Authors:  Barbara Cardazzo; Luca Bargelloni; Luisa Toffolatti; Paola Rimessi; Alessandra Ferlini; Tomaso Patarnello
Journal:  J Mol Evol       Date:  2003       Impact factor: 2.395

7.  An intronic LINE-1 element insertion in the dystrophin gene aborts dystrophin expression and results in Duchenne-like muscular dystrophy in the corgi breed.

Authors:  Bruce F Smith; Yongping Yue; Philip R Woods; Joe N Kornegay; Jin-Hong Shin; Regina R Williams; Dongsheng Duan
Journal:  Lab Invest       Date:  2010-08-16       Impact factor: 5.662

8.  Identification of a new intronic BMPR2-mutation and early diagnosis of heritable pulmonary arterial hypertension in a large family with mean clinical follow-up of 12 years.

Authors:  Katrin Hinderhofer; Christine Fischer; Nicole Pfarr; Justyna Szamalek-Hoegel; Mona Lichtblau; Christian Nagel; Benjamin Egenlauf; Nicola Ehlken; Ekkehard Grünig
Journal:  PLoS One       Date:  2014-03-12       Impact factor: 3.240

9.  Exonization of an Intronic LINE-1 Element Causing Becker Muscular Dystrophy as a Novel Mutational Mechanism in Dystrophin Gene.

Authors:  Ana Gonçalves; Jorge Oliveira; Teresa Coelho; Ricardo Taipa; Manuel Melo-Pires; Mário Sousa; Rosário Santos
Journal:  Genes (Basel)       Date:  2017-10-03       Impact factor: 4.096

10.  Pseudoexons of the DMD Gene.

Authors:  Niall P Keegan
Journal:  J Neuromuscul Dis       Date:  2020
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