Mouse Gene Set: KUNINGER_IGF1_VS_PDGFB_TARGETS_DN

For the Human gene set with the same name, see KUNINGER_IGF1_VS_PDGFB_TARGETS_DN

Standard name KUNINGER_IGF1_VS_PDGFB_TARGETS_DN
Systematic name MM1174
Brief description Genes down-regulated in C2AS12 cells (myoblast) by IGF1 [GeneID=3479] vs PDGFB [GeneID=5155].
Full description or abstract Peptide growth factors regulate cell fate by activating distinct signal transduction pathways that ultimately influence gene expression. Insulin-like growth factors (IGFs) play central roles in controlling somatic growth and participate in skeletal muscle development and regeneration. In cultured muscle cells, IGF action is critical both for maintaining viability during the transition from proliferating to differentiating myoblasts and for facilitating differentiation. By contrast, platelet-derived growth factor (PDGF) can sustain cell survival but inhibits differentiation. Here we examine the genetic programs that accompany IGF and PDGF action in myoblasts. Through analysis of high-density oligonucleotide arrays containing approximately 36,000 mouse probe sets, we identify 90 transcripts differentially induced by IGF-I, including 28 muscle-specific genes and 33 previously unannotated mRNAs, and 55 transcripts specifically stimulated by PDGF, including 14 unknowns. Detailed study of one IGF-induced mRNA shows that it encodes a protein related to a recently characterized repulsive guidance molecule postulated to regulate neuronal targeting during development. Our results demonstrate the power of transcriptional profiling for gene discovery and provide opportunities for investigating new proteins potentially involved in different aspects of growth factor action in muscle.
Collection M2: Curated
      CGP: Chemical and Genetic Perturbations
Source publication Pubmed 15475267   Authors: Kuninger D,Kuzmickas R,Peng B,Pintar JE,Rotwein P
Exact source Table 2
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Source species Mus musculus
Contributed by John Newman (University of Washington)
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identifier namespace		 AFFY_MG_U74
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Version history 2022.1.Mm: First Introduced.

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