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Series GSE6011 Query DataSets for GSE6011
Status Public on Dec 25, 2006
Title Expression data from quadriceps muscle of young DMD patients and age matched controls
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Albeit increased serum CK level and abnormal muscle histology are always present, boys with DMD are phenotipically indistinguishable from the normal ones at birth and, in their first years of life, acquire early motor milestones at normal times. A clear defect in muscle function becomes generally apparent by the end of the second year. As the disease is typically diagnosed between the ages of 3 and 7, the first two years are often considered and referred to as clinically presymptomatic.
As a defined gene expression signature was shown to characterize these symptomatic patients we sought to investigate whether and to which extent alterations may be also present in muscle from presymptomatic DMD infants. To this aim, we used the Affymetrix technology to compare the individual expression profiles of 19 DMD patients with age at biopsy scattered along the first two years of the disease with those of 14 age matched controls. This approach allowed us to describe with high resolution the altered transcriptional state that characterizes this early, presymptomatic phase of the disease and highlight some molecular pathways as potential critical targets in the pathophysiology of the disease.
Keywords: two populations study
 
Overall design -Subjects
Relevant data about the participants are posted under supplementary material (Table ST1). All DMD patients (n=22) had diagnosis of Duchenne Muscular Dystrophy based on the absence of dystrophin immunoreactivity on quadriceps muscle sections. None of the participants at the time of biopsy was or had been under corticosteroid treatment. Control biopsies (n=14) were selected from diagnostic specimens which were not given a diagnosis of neuromuscular disease nor showed any non-specific myopathic signs. A MIAME compliant description of this study is posted under supplementary Material (MIAME compliance).
-RNA extraction.
Total RNA was extracted from frozen quadriceps muscle biopsies by TriZol. (TriZol reagent, Invitrogen). RNA was further purified using the RNAeasy mini kit following the RNA cleanup protocol as indicated by the manufacturer (QIAGEN). RNA purity and integrity was assessed by spectophotometric analysis and agarose gel electrophoresis.
-Affymetrix Genechips.
In this work we made use of one chip type: the affymetrix HG-U133A genechipCRNA synthesis was performed using 5ug of total RNA as template, as described in the Affymetrix Gene Expression Manual. Genechips were washed and stained in an Affymetrix fluidic station 430. To avoid overcorrelation, samples were processed 8 at the time and arranged to have both DMD and control samples in each experimental session.
 
Contributor(s) Pescatori M, Ricci E, Bernardini C, Tonali PA
Citation(s) 17264171
Submission date Oct 10, 2006
Last update date Aug 10, 2018
Contact name Mario Pescatori
E-mail(s) mariopescatori@gmail.com
Phone 00393930761013
Organization name Health e-genomics
Street address Westplein 11
City rotterdam
ZIP/Postal code 3016BM
Country Netherlands
 
Platforms (1)
GPL96 [HG-U133A] Affymetrix Human Genome U133A Array
Samples (37)
GSM139501 normal skeletal muscle, biological rep1
GSM139502 normal skeletal muscle, biological rep2
GSM139503 normal skeletal muscle, biological rep3
Relations
BioProject PRJNA97809

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE6011_MIAME_compliance.pdf 15.1 Kb (ftp)(http) PDF
GSE6011_Patient_data_(Table_ST1_).pdf 33.4 Kb (ftp)(http) PDF
GSE6011_RAW.tar 128.5 Mb (http)(custom) TAR (of CEL)

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