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Isolation of Human Myoblasts, Assessment of Myogenic Differentiation, and Store-operated Calcium Entry Measurement
Published on: July 26, 2017
CCAAT/Enhancer Binding Protein β inhibits myogenic differentiation via ID3
Hamood AlSudais1, Neena Lala-Tabbert2, Nadine Wiper-Bergeron3
1Graduate Program in Cellular and Molecular Medicine, Faculty of Medicine, University of Ottawa, 451 Smyth Road, Ottawa, Ontario, K1H 8M5, Canada.
Abstract:
Myogenesis is regulated by the coordinated expression of muscle regulatory factors, a family of transcription factors that includes MYOD, MYF5, myogenin and MRF4. Muscle regulatory factors are basic helix-loop-helix transcription factors that heterodimerize with E proteins to bind the regulatory regions of target genes. Their activity can be inhibited by members of the Inhibitor of DNA binding and differentiation (ID) family, which bind E-proteins with high affinity, thereby preventing muscle regulatory factor-dependent transcriptional responses. CCAAT/Enhancer Binding protein beta (C/EBPβ) is a transcription factor expressed in myogenic precursor cells that acts to inhibit myogenic differentiation, though the mechanism remains poorly understood. We identify Id3 as a novel C/EBPβ target gene that inhibits myogenic differentiation. Overexpression of C/EBPβ stimulates Id3 mRNA and protein expression, and is required for C/EBPβ-mediated inhibition of myogenic differentiation. Misexpression of C/EBPβ in myogenic precursors, such as in models of cancer cachexia, prevents the differentiation of myogenic precursors and we show that loss of Id3 rescues differentiation under these conditions, suggesting that the stimulation of Id3 expression by C/EBPβ is an important mechanism by which C/EBPβ inhibits myogenic differentiation.
Insights
CCAAT/Enhancer Binding protein beta (C/EBPβ) inhibits muscle development by increasing Id3 expression. Loss of Id3 rescues myogenic differentiation, revealing a key mechanism in muscle precursor cell regulation.
Area of Science:
- Molecular Biology
- Cell Biology
- Developmental Biology
Background:
- Myogenesis, or muscle development, relies on muscle regulatory factors (MRFs) like MYOD and myogenin.
- Inhibitor of DNA binding (ID) proteins can block MRF activity by binding E proteins.
- CCAAT/Enhancer Binding protein beta (C/EBPβ) inhibits muscle differentiation, but its mechanism is unclear.
Purpose of the Study:
- To elucidate the mechanism by which C/EBPβ inhibits myogenic differentiation.
- To identify novel target genes of C/EBPβ involved in muscle development.
Main Methods:
- Overexpression of C/EBPβ in myogenic precursors.
- Analysis of Id3 mRNA and protein expression.
- Assessment of myogenic differentiation markers.
- Genetic manipulation to rescue differentiation in C/EBPβ-misexpressing cells.
Main Results:
- C/EBPβ directly stimulates Id3 gene and protein expression.
- Id3 is essential for C/EBPβ-mediated inhibition of myogenic differentiation.
- Loss of Id3 function rescues muscle differentiation in models with C/EBPβ misexpression, such as cancer cachexia.
Conclusions:
- Id3 is a novel target gene of C/EBPβ.
- C/EBPβ inhibits myogenic differentiation primarily by inducing Id3 expression.
- This C/EBPβ-Id3 pathway is a critical regulator of muscle precursor cell fate.
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