학술논문

Cell-fate determination by ubiquitin-dependent regulation of translation.
Document Type
article
Source
Nature. 525(7570)
Subject
Ribosomes
Neural Crest
Animals
Xenopus
Humans
Mandibulofacial Dysostosis
Cullin Proteins
RNA Polymerase I
Adaptor Proteins
Signal Transducing
Nuclear Proteins
Phosphoproteins
Ubiquitin
Proteomics
Cell Differentiation
Protein Biosynthesis
Embryonic Stem Cells
Ubiquitination
Adaptor Proteins
Signal Transducing
General Science & Technology
Language
Abstract
Metazoan development depends on the accurate execution of differentiation programs that allow pluripotent stem cells to adopt specific fates. Differentiation requires changes to chromatin architecture and transcriptional networks, yet whether other regulatory events support cell-fate determination is less well understood. Here we identify the ubiquitin ligase CUL3 in complex with its vertebrate-specific substrate adaptor KBTBD8 (CUL3(KBTBD8)) as an essential regulator of human and Xenopus tropicalis neural crest specification. CUL3(KBTBD8) monoubiquitylates NOLC1 and its paralogue TCOF1, the mutation of which underlies the neurocristopathy Treacher Collins syndrome. Ubiquitylation drives formation of a TCOF1-NOLC1 platform that connects RNA polymerase I with ribosome modification enzymes and remodels the translational program of differentiating cells in favour of neural crest specification. We conclude that ubiquitin-dependent regulation of translation is an important feature of cell-fate determination.