A translation control module coordinates germline stem cell differentiation with ribosome biogenesis during Drosophila oogenesis

• DOI: 10.1016/j.devcel.2022.03.005
• Publication Date: 2022-04-11T14:29:09Z
• Authors: Elliot T. Martin; Patrick Blatt; Elaine Nguyen; Roni Lahr; Sangeetha Selvam; Hyun Ah M. Yoon; Tyler Pocchiari; Shamsi Emtenani; Daria E. Siekhaus; Andrea Berman; Gabriele Fuchs; Prashanth Rangan
• Keywords: ribosome biogenesis; Ribosomal protein

SummaryRibosomal defects perturb stem cell differentiation, causing diseases called ribosomopathies. How ribosome levels control stem cell differentiation is not fully known. Here, we discovered three RNA helicases are required for ribosome biogenesis and forDrosophilaoogenesis. Loss of these helicases, which we named Aramis, Athos and Porthos, lead to aberrant stabilization of p53, cell cycle arrest and stalled GSC differentiation. Unexpectedly, Aramis is required for efficient translation of a cohort of mRNAs containing a 5’-Terminal-Oligo-Pyrimidine (TOP)-motif, including mRNAs that encode ribosomal proteins and a conserved p53 inhibitor,NovelNucleolar protein 1 (Non1). The TOP-motif co-regulates the translation of growth-related mRNAs in mammals. As in mammals, the La-related protein co-regulates the translation of TOP-motif containing RNAs duringDrosophilaoogenesis. Thus, a previously unappreciated TOP-motif inDrosophilaresponds to reduced ribosome biogenesis to co-regulate the translation of ribosomal proteins and a p53 repressor, thus coupling ribosome biogenesis to GSC differentiation.