Literature DB >> 11223239

The dystrophin / utrophin homologues in Drosophila and in sea urchin.

S Neuman1, A Kaban, T Volk, D Yaffe, U Nudel.   

Abstract

The gene which is defective in Duchenne muscular dystrophy (DMD) is the largest known gene containing at least 79 introns, some of which are extremely large. The product of the gene in muscle, dystrophin, is a 427 kDa protein. The same gene encodes at least two additional non-muscle full length dystrophin isoforms transcribed from different promoters located in the 5'-end region of the gene, and four smaller proteins transcribed from internal promoters located further downstream, and lack important domains of dystrophin. Several other genes, encoding evolutionarily related proteins, have been identified. To study the evolution of the DMD gene and the significance of its various products, we have searched for genes encoding dystrophin-like proteins in sea urchin and in Drosophila. We previously reported on the characterization of a sea urchin gene encoding a protein which is an evolutionary homologue of Dp116, one of the small products of the mammalian DMD gene, and on the partial sequencing of a large product of the same gene. Here we describe the full-length product which shows strong structural similarity and sequence identity to human dystrophin and utrophin. We also describe a Drosophila gene closely related to the human dystrophin gene. Like the human gene, the Drosophila gene encodes at least three isoforms of full length dystrophin-like proteins (dmDLP1, dmDLP2 and dmDLP3,), regulated by different promoters located at the 5' end of the gene, and a smaller product regulated by an internal promoter (dmDp186). As in mammals, dmDp186 and the dmDLPs share the same C-terminal and cysteine-rich domains which are very similar to the corresponding domains in human dystrophin and utrophin. In addition, dmDp186 contains four of the spectrin-like repeats of the dmDLPs and a unique N-terminal region of 512 amino acids encoded by a single exon. The full length products and the small product have distinct patterns of expression. Thus, the complex structure of the dystrophin gene, encoding several large dystrophin-like isoforms and smaller truncated products with different patterns of expression, existed before the divergence between the protostomes and deuterostomes. The conservation of this gene structure in such distantly related organisms, points to important distinct functions of the multiple products.

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Year:  2001        PMID: 11223239     DOI: 10.1016/s0378-1119(00)00584-9

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  15 in total

Review 1.  Duchenne's muscular dystrophy: animal models used to investigate pathogenesis and develop therapeutic strategies.

Authors:  C A Collins; J E Morgan
Journal:  Int J Exp Pathol       Date:  2003-08       Impact factor: 1.925

2.  Dystrophin is required for appropriate retrograde control of neurotransmitter release at the Drosophila neuromuscular junction.

Authors:  Mariska C van der Plas; Gonneke S K Pilgram; Jaap J Plomp; Anja de Jong; Lee G Fradkin; Jasprina N Noordermeer
Journal:  J Neurosci       Date:  2006-01-04       Impact factor: 6.167

Review 3.  Duchenne muscular dystrophy animal models for high-throughput drug discovery and precision medicine.

Authors:  Nalinda B Wasala; Shi-Jie Chen; Dongsheng Duan
Journal:  Expert Opin Drug Discov       Date:  2020-01-30       Impact factor: 6.098

4.  Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy.

Authors:  Halyna R Shcherbata; Andriy S Yatsenko; Larissa Patterson; Vanita D Sood; Uri Nudel; David Yaffe; David Baker; Hannele Ruohola-Baker
Journal:  EMBO J       Date:  2007-01-11       Impact factor: 11.598

5.  Utrophin binds laterally along actin filaments and can couple costameric actin with sarcolemma when overexpressed in dystrophin-deficient muscle.

Authors:  Inna N Rybakova; Jitandrakumar R Patel; Kay E Davies; Peter D Yurchenco; James M Ervasti
Journal:  Mol Biol Cell       Date:  2002-05       Impact factor: 4.138

Review 6.  Other model organisms for sarcomeric muscle diseases.

Authors:  John Sparrow; Simon M Hughes; Laurent Segalat
Journal:  Adv Exp Med Biol       Date:  2008       Impact factor: 2.622

7.  Chronic hypoxia impairs muscle function in the Drosophila model of Duchenne's muscular dystrophy (DMD).

Authors:  Matias Mosqueira; Gabriel Willmann; Hannele Ruohola-Baker; Tejvir S Khurana
Journal:  PLoS One       Date:  2010-10-20       Impact factor: 3.240

8.  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

9.  Dystroglycan and protein O-mannosyltransferases 1 and 2 are required to maintain integrity of Drosophila larval muscles.

Authors:  Nicola Haines; Sara Seabrooke; Bryan A Stewart
Journal:  Mol Biol Cell       Date:  2007-09-19       Impact factor: 4.138

Review 10.  The roles of the dystrophin-associated glycoprotein complex at the synapse.

Authors:  Gonneke S K Pilgram; Saranyapin Potikanond; Richard A Baines; Lee G Fradkin; Jasprina N Noordermeer
Journal:  Mol Neurobiol       Date:  2009-11-09       Impact factor: 5.590

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