8ESQ

Ytm1 associated nascent 60S ribosome State 2

This is a non-PDB format compatible entry.

Summary for 8ESQ

• Entry DOI: 10.2210/pdb8esq/pdb
• EMDB information: 24411
• Descriptor: Noc2, ATP-dependent RNA helicase has1, 60S ribosomal protein L6, ... (59 entities in total)
• Functional Keywords: nucleophosmin, ribosome biogenesis, fkbp, 60s ribosome, ribosome
• Biological source: Schizosaccharomyces pombe (fission yeast); More
• Total number of polymer chains: 58
• Total formula weight: 2984039.65

Authors

Zhou, X.,Bilokapic, S.,Deshmukh, A.A.,Halic, M. (deposition date: 2022-10-14, release date: 2022-11-30, Last modification date: 2024-06-19)

Primary citation

Ugolini, I.,Bilokapic, S.,Ferrolino, M.,Teague, J.,Yan, Y.,Zhou, X.,Deshmukh, A.,White, M.,Kriwacki, R.W.,Halic, M.
Chromatin localization of nucleophosmin organizes ribosome biogenesis.
Mol.Cell, 82:4443-, 2022

PubMed Abstract: Ribosome biogenesis takes place in the nucleolus, a nuclear membrane-less organelle. Although well studied, it remains unknown how nascent ribosomal subunits separate from the central chromatin compartment and move to the outer granular component, where maturation occurs. We find that the Schizosaccharomyces pombe nucleophosmin-like protein Fkbp39 localizes to rDNA sites encoding the 60S subunit rRNA, and this localization contributes to its specific association with nascent 60S subunits. Fkbp39 dissociates from chromatin to bind nascent 60S subunits, causing the latter to partition away from chromatin and from nascent 40S subunits through liquid-liquid phase separation. In vivo, Fkbp39 binding directs the translocation of nascent 60S subunits toward the nucleophosmin-rich granular component. This process increases the efficiency of 60S subunit assembly, facilitating the incorporation of 60S RNA domain III. Thus, chromatin localization determines the specificity of nucleophosmin in sorting nascent ribosomal subunits and coordinates their movement into specialized assembly compartments within the nucleolus.

PubMed: 36423630
DOI: 10.1016/j.molcel.2022.10.033

Experimental method

ELECTRON MICROSCOPY (2.8 Å)