TY - JOUR
T1 - Large-scale gene expression analysis of human skeletal myoblast differentiation
AU - Sterrenburg, Ellen
AU - Turk, Rolf
AU - 'T Hoen, Peter A.C.
AU - Van Deutekom, Judith C.T.
AU - Boer, Judith M.
AU - Van Ommen, Gert Jan B.
AU - Den Dunnen, Johan T.
N1 - Funding Information:
We would like to thank Renée X. de Menezes (Medical Statistics, LUMC) and Stefan White (Human Genetics, LUMC) for critical reading of the manuscript and valuable suggestions. We would like to thank the Leiden Genome Technology Center for providing the oligonucleotide arrays. This work was supported by grants from the Nederlandse Organisatie voor Wetenschappelijk Onderzoek (NWO, NL) and the Muscular Dystrophy Campaign (MDC, UK).
PY - 2004/9
Y1 - 2004/9
N2 - To study pathways involved in human skeletal myogenesis, we profiled gene expression in human primary myoblast cells derived from three individuals using both oligonucleotide and cDNA microarrays. Following stringent statistical testing (false-positive rate 0.4%), we identified 146 genes differentially expressed over time. Interestingly, 86 of these genes have not been reported to be involved in myogenesis in mouse cell lines. This demonstrates the additional value of human primary cell cultures in the study of muscle differentiation. Many of the identified genes play a role in muscle regeneration, indicating the close relationship of this process with muscle development. In addition, we found overlap with expression profiling studies in muscle from Duchenne muscular dystrophy patients, confirming ongoing muscle regeneration in Duchenne muscular dystrophy. Further study of these genes can bring new insights into the process of muscle differentiation, and they are candidate genes for neuromuscular disorders with an as yet unidentified cause.
AB - To study pathways involved in human skeletal myogenesis, we profiled gene expression in human primary myoblast cells derived from three individuals using both oligonucleotide and cDNA microarrays. Following stringent statistical testing (false-positive rate 0.4%), we identified 146 genes differentially expressed over time. Interestingly, 86 of these genes have not been reported to be involved in myogenesis in mouse cell lines. This demonstrates the additional value of human primary cell cultures in the study of muscle differentiation. Many of the identified genes play a role in muscle regeneration, indicating the close relationship of this process with muscle development. In addition, we found overlap with expression profiling studies in muscle from Duchenne muscular dystrophy patients, confirming ongoing muscle regeneration in Duchenne muscular dystrophy. Further study of these genes can bring new insights into the process of muscle differentiation, and they are candidate genes for neuromuscular disorders with an as yet unidentified cause.
KW - Gene expression
KW - Microarray
KW - Muscle differentiation
KW - Myogenesis
UR - http://www.scopus.com/inward/record.url?scp=4344608388&partnerID=8YFLogxK
U2 - 10.1016/j.nmd.2004.03.008
DO - 10.1016/j.nmd.2004.03.008
M3 - Article
C2 - 15336692
AN - SCOPUS:4344608388
SN - 0960-8966
VL - 14
SP - 507
EP - 518
JO - Neuromuscular Disorders
JF - Neuromuscular Disorders
IS - 8-9
ER -