Ringo: Discordance between the molecular and clinical manifestation in a Golden Retriever Muscular Dystrophy dog


Autoria(s): ZUCCONI, Eder; VALADARES, Marcos Costa; VIEIRA, Natassia M.; BUENO JR., Carlos R.; SECCO, Mariane; JAZEDJE, Tatiana; SILVA, Helga Cristina Almeida da; VAINZOF, Mariz; ZATZ, Mayana
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

18/10/2012

18/10/2012

2010

Resumo

Of the various genetic homologues to Duchenne Muscular Dystrophy (DMD), the Golden Retriever Muscular Dystrophy (GRMD) dog, which presents a variable but usually severe and progressive muscle weakness, has the closest relevance to DMD in both clinical severity and histopathological change. Among 77 GRMD dogs born in our colony in Brazil, we have identified a very mildly affected dog, Ringo, born July 2003. Among his descendants, at least one male, Suflair, is also showing a mild course. In an attempt to better characterize these two dogs, we studied the pattern of muscle proteins expression in Ringo and Suflair, as compared to severely affected and normal control dogs. Dystrophin was absent in both and utrophin was overexpressed in a pattern similar to the observed in severely affected dogs. Understanding the mechanism that is protecting Ringo and Suflair from the deleterious effect of the dystrophin gene mutation is of utmost interest, In addition it points out that the clinical impact of therapeutic trials should be interpreted with caution. (C) 2009 Elsevier B.V. All rights reserved.

CEPID-FAPESP

CNPq-INCT

FINEP

ABDIM

Identificador

NEUROMUSCULAR DISORDERS, AMSTERDAM, v.20, n.1, p.64-70, JAN, 2010

0960-8966

http://producao.usp.br/handle/BDPI/17424

10.1016/j.nmd.2009.10.011

http://dx.doi.org/10.1016/j.nmd.2009.10.011

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

AMSTERDAM

Relação

Neuromuscular Disorders

Direitos

restrictedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #Golden Retriever Muscular Dystrophy #Duchenne Muscular Dystrophy #Dystrophin #Mild phenotype #MUSCLE #UTROPHIN #MOUSE #CELLS #Clinical Neurology #Neurosciences
Tipo

article

original article

publishedVersion