Literature DB >> 8392588

A cluster of transposon-like repetitive sequences in intron 7 of the human dystrophin gene.

J C McNaughton1, J E Broom, D F Hill, W A Jones, C J Marshall, N M Renwick, P A Stockwell, G B Petersen.   

Abstract

A 32 kilobase-pair fragment of intron 7 of the human dystrophin gene has been sequenced and analysed for the presence of repetitive elements and open reading frames. Two transposon-like human elements (THE-1 sequences), and three intervening, and related, long terminal repeat elements, together with three Alu sequences and a LINE sequence have been identified. These represent an unexpected clustering of highly-repetitive sequences within this single segment of intron DNA. Amplification of a region of chimpanzee genomic DNA by the polymerase chain reaction has provided evidence that at least one of the THE-1 sequences is present in the same position in the chimpanzee genome and the high homology between the human and chimpanzee sequences indicates that this element was fixed within the ancestral genome before the divergence of the two species. The possible role of repetitive, transposon-like sequences in natural mutagenesis of the dystrophin gene is discussed.

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Year:  1993        PMID: 8392588     DOI: 10.1006/jmbi.1993.1389

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  9 in total

1.  Phylogenetic relationships among transposon-like elements in human and primate DNA.

Authors:  J C McNaughton; C J Marshall; J E Broom; G Hughes; W A Jones; P A Stockwell; G B Petersen
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Review 4.  Evolution and biological significance of human retroelements.

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Journal:  Curr Genomics       Date:  2013-08       Impact factor: 2.236

6.  A study on duplications of the dystrophin gene: evidence of a geographical difference in the distribution of breakpoints by intron.

Authors:  F Galvagni; F A Saad; G A Danieli; M Miorin; L Vitiello; M L Mostacciuolo; C Angelini
Journal:  Hum Genet       Date:  1994-07       Impact factor: 4.132

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.

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8.  Deletion of Dystrophin In-Frame Exon 5 Leads to a Severe Phenotype: Guidance for Exon Skipping Strategies.

Authors:  Zhi Yon Charles Toh; May Thandar Aung-Htut; Gavin Pinniger; Abbie M Adams; Sudarsan Krishnaswarmy; Brenda L Wong; Sue Fletcher; Steve D Wilton
Journal:  PLoS One       Date:  2016-01-08       Impact factor: 3.240

9.  Genome-wide association study to identify potential genetic modifiers in a canine model for Duchenne muscular dystrophy.

Authors:  Candice Brinkmeyer-Langford; Cynthia Balog-Alvarez; James J Cai; Brian W Davis; Joe N Kornegay
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  9 in total

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