Mushtaq, M;
              
      
            
                Kovalevska, L;
              
      
            
                Darekar, S;
              
      
            
                Abramsson, A;
              
      
            
                Zetterberg, H;
              
      
            
                Kashuba, V;
              
      
            
                Klein, G;
              
      
            
            
          
      
            
            
            ... Kashuba, E; + view all
            
          
      
        
        
        
    
  
(2020)
  Cell stemness is maintained upon concurrent expression of RB and the mitochondrial ribosomal protein S18-2.
Proceedings of the National Academy of Sciences of the United States of America
      
    
    
    
         10.1073/pnas.1922535117.
   (In press).
  
       
    
  
| Preview | Text 1922535117.full.pdf - Accepted Version Download (2MB) | Preview | 
Abstract
Stemness encompasses the capability of a cell for self-renewal and differentiation. The stem cell maintains a balance between proliferation, quiescence, and regeneration via interactions with the microenvironment. Previously, we showed that ectopic expression of the mitochondrial ribosomal protein S18-2 (MRPS18-2) led to immortalization of primary fibroblasts, accompanied by induction of an embryonic stem cell (ESC) phenotype. Moreover, we demonstrated interaction between S18-2 and the retinoblastoma-associated protein (RB) and hypothesized that the simultaneous expression of RB and S18-2 is essential for maintaining cell stemness. Here, we experimentally investigated the role of S18-2 in cell stemness and differentiation. Concurrent expression of RB and S18-2 resulted in immortalization of Rb1−/− primary mouse embryonic fibroblasts and in aggressive tumor growth in severe combined immunodeficiency mice. These cells, which express both RB and S18-2 at high levels, exhibited the potential to differentiate into various lineages in vitro, including osteogenic, chondrogenic, and adipogenic lineages. Mechanistically, S18-2 formed a multimeric protein complex with prohibitin and the ring finger protein 2 (RNF2). This molecular complex increased the monoubiquitination of histone H2ALys119, a characteristic trait of ESCs, by enhanced E3-ligase activity of RNF2. Furthermore, we found enrichment of KLF4 at the S18-2 promoter region and that the S18-2 expression is positively correlated with KLF4 levels. Importantly, knockdown of S18-2 in zebrafish larvae led to embryonic lethality. Collectively, our findings suggest an important role for S18-2 in cell stemness and differentiation and potentially also in cancerogenesis.
| Type: | Article | 
|---|---|
| Title: | Cell stemness is maintained upon concurrent expression of RB and the mitochondrial ribosomal protein S18-2 | 
| Location: | United States | 
| Open access status: | An open access version is available from UCL Discovery | 
| DOI: | 10.1073/pnas.1922535117 | 
| Publisher version: | https://doi.org/10.1073/pnas.1922535117 | 
| Language: | English | 
| Additional information: | This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND). https://creativecommons.org/licenses/by-nc-nd/4.0/ | 
| Keywords: | cell immortalization, embryogenesis, stemness and differentiation, tumorigenesis | 
| UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Neurodegenerative Diseases | 
| URI: | https://discovery.ucl.ac.uk/id/eprint/10103832 | 
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