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Updated: Jun 19, 2026

Chromatographic Purification of Highly Active Yeast Ribosomes
Published on: October 24, 2011
The effect of puromycin on intranuclear steps in ribosome biosynthesis
R Soeiro1, M H Vaughan, J E Darnell
1Department of Biochemistry, the Albert Einstein College of Medicine of Yeshiva University, New York 10461.
Abstract:
Inhibition of protein synthesis by puromycin (100 gamma/ml) is known to inhibit the synthesis of ribosomes. However, ribosomal precursor RNA (45S) continues to be synthesized, methylated, and processed. Cell fractionation studies revealed that, although the initial processing (45S --> 32S + 16S) occurs in the presence of puromycin, the 16S moiety is immediately degraded. No species of ribosomal RNA can be found to have emerged from the nucleolus. The RNA formed in the presence of puromycin is normal as judged by its ability to enter new ribosomal particles after puromycin is removed. This sequence of events is not a result of inhibition of protein synthesis, for cycloheximide, another inhibitor of protein synthesis, either alone or in combination with puromycin allows the completion of new ribosomes.
Insights
Puromycin inhibits ribosome synthesis by degrading ribosomal RNA (rRNA) precursors. This rRNA degradation, not protein synthesis inhibition, prevents new ribosome formation. Cycloheximide demonstrates this distinction.
Area of Science:
- Molecular Biology
- Cell Biology
- Biochemistry
Background:
- Puromycin inhibits protein synthesis and is known to affect ribosome synthesis.
- Ribosomal RNA (rRNA) synthesis, methylation, and initial processing continue despite puromycin treatment.
Purpose of the Study:
- To investigate the specific mechanism by which puromycin inhibits ribosome biogenesis.
- To differentiate the effects of protein synthesis inhibition from direct effects on rRNA processing and ribosome assembly.
Main Methods:
- Cell fractionation studies were employed to analyze RNA processing and localization.
- Puromycin and cycloheximide were used as protein synthesis inhibitors to compare their effects.
Main Results:
- Puromycin treatment leads to the degradation of the 16S rRNA moiety after initial processing of the 45S precursor.
- No mature ribosomal RNA species were observed to exit the nucleolus in the presence of puromycin.
- RNA synthesized during puromycin treatment remained functional for new ribosome assembly upon drug removal.
- Cycloheximide, another protein synthesis inhibitor, did not cause rRNA degradation and allowed new ribosome completion, alone or with puromycin.
Conclusions:
- Puromycin's inhibition of ribosome synthesis is primarily due to the degradation of rRNA precursors, not solely the inhibition of protein synthesis.
- The nucleolus is the site of initial rRNA processing, but subsequent maturation and export are blocked by puromycin.
- The observed effects are specific to puromycin's action on rRNA stability, distinct from general protein synthesis inhibition.
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