HMGB proteins involved in TOR signaling as general regulators of cell growth by controlling ribosome biogenesis.
A Vizoso-VázquezA Barreiro-AlonsoM I González-SisoE Rodríguez-BelmonteM Lamas-MaceirasMaría Esperanza CerdánPublished in: Current genetics (2018)
The number of ribosomes and their activity need to be highly regulated because their function is crucial for the cell. Ribosome biogenesis is necessary for cell growth and proliferation in accordance with nutrient availability and other external and intracellular signals. High-mobility group B (HMGB) proteins are conserved from yeasts to human and are decisive in cellular fate. These proteins play critical functions, from the maintenance of chromatin structure, DNA repair, or transcriptional regulation, to facilitation of ribosome biogenesis. They are also involved in cancer and other pathologies. In this review, we summarize evidence of how HMGB proteins contribute to ribosome-biogenesis control, with special emphasis on a common nexus to the target of rapamycin (TOR) pathway, a signaling cascade essential for cell growth and proliferation from yeast to human. Perspectives in this field are also discussed.
Keyphrases
- dna repair
- transcription factor
- endothelial cells
- dna damage
- induced pluripotent stem cells
- gene expression
- pluripotent stem cells
- single cell
- papillary thyroid
- squamous cell carcinoma
- saccharomyces cerevisiae
- genome wide
- dna damage response
- cell therapy
- dna methylation
- mesenchymal stem cells
- squamous cell
- oxidative stress
- bone marrow
- quality control