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The potential role of ribosomal protein S5 on cell cycle arrest and initiation of murine erythroleukemia cell differentiation
Author(s) -
Matragkou Christi.,
Papachristou Eleni T.,
Tezias Sotirios S.,
Tsiftsoglou Asterios S.,
CholiPapadopoulou Theodora,
Vizirianakis Ioannis S.
Publication year - 2008
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.21722
Subject(s) - microbiology and biotechnology , cell cycle , cell , ribosomal protein , cell cycle checkpoint , chemistry , biology , biochemistry , ribosome , rna , gene
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.