The potential role of ribosomal protein S5 on cell cycle arrest and initiation of murine erythroleukemia cell differentiation

✍ Scribed by Christina N. Matragkou; Eleni T. Papachristou; Sotirios S. Tezias; Asterios S. Tsiftsoglou; Theodora Choli-Papadopoulou; Ioannis S. Vizirianakis

• Publisher: John Wiley and Sons
• Year: 2008
• Tongue: English
• Weight: 650 KB
• Volume: 104
• Category: Article
• ISSN: 0730-2312
• DOI: 10.1002/jcb.21722

✦ Synopsis

Abstract

Evidence now exists to indicate that some ribosomal proteins besides being structural components of the ribosomal subunits are involved in the regulation of cell differentiation and apoptosis. As we have shown earlier, initiation of erythroid differentiation of murine erythroleukemia (MEL) cells is associated with transcriptional inactivation of genes encoding ribosomal RNAs and ribosomal proteins S5 (RPS5) and L35a. In this study, we extended these observations and investigated whether transfection of MEL cells with RPS5 cDNA affects the onset of initiation of erythroid maturation and their entrance in cell cycle arrest. Stably transfected MEL cloned cells (MEL‐C14 and MEL‐C56) were established and assessed for their capacity to produce RPS5 RNA transcript and its translated product. The impact of RPS5 cDNA transfection on the RPS5 gene expression patterns and the accumulation of RPS5 protein in inducible transfected MEL cells were correlated with their ability to: (a) initiate differentiation, (b) enter cell cycle arrest at G~1~/G~0~ phase, and (c) modulate the level of cyclin‐dependent kinases CDK2, CDK4, and CDK6. The data presented indicate that deregulation of RPS5 gene expression (constitutive expression) affects RPS5 protein level and delays both the onset of initiation of erythroid maturation and entrance in cell cycle arrest in inducer‐treated MEL cells. J. Cell. Biochem. 104: 1477–1490, 2008. © 2008 Wiley‐Liss, Inc.