Nog2p, a putative GTPase associated with pre-60S subunits and required for late 60S maturation steps
Abstract
Eukaryotic ribosome maturation depends on a set of well ordered processing steps. Here we describe the functional characterization of yeast Nog2p (Ynr053cp), a highly conserved nuclear protein. Nog2p contains a putative GTP-binding site, which is essential in vivo. Kinetic and steady-state measurements of the levels of pre-rRNAs in Nog2p-depleted cells showed a defect in 5.8S and 25S maturation and a concomitant increase in the levels of both 27SB(S) and 7S(S) precursors. We found Nog2p physically associated with large pre-60S complexes highly enriched in the 27SB and 7S rRNA precursors. These complexes contained, besides a subset of ribosomal proteins, at least two additional factors, Nog1p, another putative GTP-binding protein, and Rlp24p (Ylr009wp), which belongs to the Rpl24e family of archaeal and eukaryotic ribosomal proteins. In the absence of Nog2p, the pre-60S ribosomal complexes left the nucleolus, but were retained in the nucleoplasm. These results suggest that transient, possibly GTP-dependent association of Nog2p with the pre-ribosomes might trigger late rRNA maturation steps in ribosomal large subunit biogenesis.
Keywords
Active Transport
Cell Nucleus
Alternative Splicing
Amino Acid Sequence
Binding Sites
Blotting
Northern
Cell Nucleolus
Cytoplasm
DNA
Complementary
Genotype
Glucose
Green Fluorescent Proteins
GTP-Binding Proteins
GTP Phosphohydrolases
Humans
In Situ Hybridization
Kinetics
Luminescent Proteins
Mass Spectrometry
Microscopy
Electron
Fluorescence
Models
Genetic
Molecular Sequence Data
Plasmids
Polyribosomes
Promoter Regions
Protein Binding
Ribosomes
RNA
Messenger
Ribosomal
Sequence Homology
Amino Acid
Time Factors
Domains
Life Sciences [q-bio]
Origin : Publication funded by an institution
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