Ribonuclease inhibitor and angiogenin system regulates cell type-specific global translation.
Martina StillinovicMayuresh Anant SarangdharNicola AndinaAubry TardivelFrédéric GreubGiuseppe BombaciCamille AnsermetMarco ZattiDipanjali SahaJieyu XiongTakeru SagaeMariko YokogawaMasanori OsawaManfred HellerAdrian KeoghIrene KellerAnne Angelillo-ScherrerRamanjaneyulu AllamPublished in: Science advances (2024)
Translation of mRNAs is a fundamental process that occurs in all cell types of multicellular organisms. Conventionally, it has been considered a default step in gene expression, lacking specific regulation. However, recent studies have documented that certain mRNAs exhibit cell type-specific translation. Despite this, it remains unclear whether global translation is controlled in a cell type-specific manner. By using human cell lines and mouse models, we found that deletion of the ribosome-associated protein ribonuclease inhibitor 1 (RNH1) decreases global translation selectively in hematopoietic-origin cells but not in the non-hematopoietic-origin cells. RNH1-mediated cell type-specific translation is mechanistically linked to angiogenin-induced ribosomal biogenesis. Collectively, this study unravels the existence of cell type-specific global translation regulators and highlights the complex translation regulation in vertebrates.