Signaling networks and intrinsic mechanisms that regulate the production of ribosomes in transformed cells

• Autores: Natalia Fernández Parejo
• Directores de la Tesis: Xosé R. García Bustelo (dir. tes.), Mercedes Dosil Castro (codir. tes.)
• Lectura: En la Universidad de Salamanca ( España ) en 2023
• Idioma: español
• Tribunal Calificador de la Tesis: José Luis Rosa López (presid.), Sandra Blanco Benavente (secret.), Antonio Gentilella (voc.)
• Programa de doctorado: Programa de Doctorado en Biociencias: Biología y Clínica del Cáncer y Medicina Traslacional por la Universidad de Salamanca
• Materias:
  • Ciencias de la vida
    • Biología molecular
  • Ciencias médicas
    • Patología
      • Oncología
• Enlaces
  • Tesis en acceso abierto en: GREDOS
• Resumen

  • Eukaryotic ribosomes contain four rRNAs and ~80 proteins that are assembled in two subunits of unequal sizes, the 40S and 60S subunits. The formation of the two subunits starts with the synthesis by RNA polymerase I of a pre-rRNA transcript, and is followed by the formation of the initial 40S and 60S pre-ribosomes. Those complexes then enter two separate multi-step maturation pathways that happen in the nucleolus, nucleoplasm and cytoplasm. The whole process of ribosome formation is assisted by more than 200 ribosome biogenesis factors (RBFs) that mediate the modification, folding and processing of rRNA precursors, and the incorporation of ribosomal proteins. Because ribosome synthesis is hyperactivated in many cancers there is much interest in understanding how transformed cells deregulate this process. One aspect to ascertain is which signaling pathways activate ribosome synthesis in different cell contexts. Another important aspect is to unveil all the events within the human ribosome synthesis pathway that are subject to regulation. This thesis addressed those two aspects in two separate projects. The first project focused on the study of a VAV2-mediated signaling pathway that activates ribosome production in human keratinocytes. We dissect the elements that participate in the pathway, identify the step of ribosome synthesis that is activated, and provide evidence of its deregulation and amenability to inhibition in squamous cell carcinoma. The second project was devoted to the characterization of a set of so-far undescribed intermediates of 40S subunit maturation in human cells. We define in which steps of the 40S pathway they intervene, identify a group of RBFs associated to them, and perform loss-of-function analyses to characterize their functions. Our results reveal a process that exhibits regulatory features and is required for proper production of 40S ribosomal subunits.