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Sci Adv ; 10(22): eadl0320, 2024 May 31.
Article in English | MEDLINE | ID: mdl-38820160

ABSTRACT

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.


Subject(s)
Protein Biosynthesis , Ribonuclease, Pancreatic , Ribosomes , Ribonuclease, Pancreatic/metabolism , Ribonuclease, Pancreatic/genetics , Humans , Animals , Mice , Ribosomes/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , Gene Expression Regulation , Cell Line , Organ Specificity , Carrier Proteins
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