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Updated: Apr 16, 2026

Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers
Published on: September 20, 2018
Cdk5 controls IL-2 gene expression via repression of the mSin3a-HDAC complex
Eric Lam1, Tej K Pareek, John J Letterio
1a Department of Pediatrics; Division of Pediatric Hematology/Oncology; University Hospitals Rainbow Babies & Children's Hospital Center; The Angie Fowler Adolescent & Young Adult Cancer Institute; The Case Comprehensive Cancer Center ; Case Western Reserve University ; Cleveland , OH USA.
Abstract:
Cyclin-dependent kinase 5 (Cdk5) is a unique member of a family of serine/threonine cyclin-dependent protein kinases. We previously demonstrated disruption of Cdk5 gene expression in mice impairs T-cell function and ameliorates T-cell-mediated neuroinflammation. Here, we show Cdk5 modulates gene expression during T-cell activation by impairing the repression of gene transcription by histone deacetylase 1 (HDAC1) through specific phosphorylation of the mSin3a protein at serine residue 861. Disruption of Cdk5 activity in T-cells enhances HDAC activity and binding of the HDAC1/mSin3a complex to the IL-2 promoter, leading to suppression of IL-2 gene expression. These data point to essential roles for Cdk5 in regulating gene expression in T-cells and transcriptional regulation by the co-repressor mSin3a.
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