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Updated: Jul 20, 2026

In Vivo Detection and Analysis of Rb Protein SUMOylation in Human Cells
Published on: November 2, 2017
The apoptosis modulator and tumour suppressor protein RBM5 is a phosphoprotein
Yanjun Shu1, Nina D Rintala-Maki, Vanessa E Wall
1Tumour Biology Group, Regional Cancer Program of the Hôpital régional de Sudbury Regional Hospital, Sudbury, Ontario, Canada.
Abstract:
RBM5/LUCA-15/H37 is a nuclear SR-related RNA binding protein with the ability to modulate both apoptosis and the cell cycle, and retard tumour formation. How RBM5 functions to carry out these, potentially interrelated, biological activities is unknown. Since reversible phosphorylation has been shown to play an important role in the regulation of SR protein function, apoptosis and cell cycle control, in an attempt to elucidate the underlying mechanisms regulating RBM5 function, the phosphorylation status of RBM5 was investigated. Whole cell lysate from growing cell cultures was treated with the broad phosphatase spectrum of CIP, resulting in a decrease in the molecular mass of RBM5. A similar decrease in molecular mass, of a subset of RBM5 proteins, was observed during growth factor deprivation, in a manner consistent with partial dephosphorylation of RBM5. Molecular mass increased upon growth factor addition, demonstrating that this apoptosis-associated alteration in molecular mass was a reversible process. Immunoprecipitation and mutagenesis experiments strongly suggested that phosphotyrosines are not present in RBM5 under normal growth conditions, and that serine 69 is phosphorylated, but not by Akt kinase. Taken together, these results suggest that reversible phosphorylation of RBM5 is a mechanism capable of regulating RBM5 participation in modulating apoptosis, and perhaps tumour suppression.
Insights
Reversible phosphorylation of RNA binding protein 5 (RBM5) regulates its role in apoptosis and tumor suppression. This dephosphorylation occurs during growth factor deprivation and is reversible, suggesting a key regulatory mechanism.
Area of Science:
- Molecular biology
- Cellular biology
- Cancer research
Background:
- RNA binding protein 5 (RBM5) influences apoptosis, cell cycle, and tumor formation.
- The precise mechanisms regulating RBM5 function remain unclear.
- Post-translational modifications, like phosphorylation, are crucial for protein regulation.
Purpose of the Study:
- To investigate the phosphorylation status of RBM5.
- To elucidate the role of RBM5 phosphorylation in regulating its biological activities.
- To understand the mechanisms controlling RBM5 function in apoptosis and tumor suppression.
Main Methods:
- Analysis of RBM5 molecular mass using phosphatase treatment and growth factor manipulation.
- Investigation of RBM5 phosphorylation changes during growth factor deprivation and addition.
- Immunoprecipitation and mutagenesis to identify phosphorylation sites and kinases.
Main Results:
- Treatment with broad-spectrum phosphatase decreased RBM5 molecular mass, indicating dephosphorylation.
- Growth factor deprivation led to RBM5 dephosphorylation, which was reversible upon growth factor addition.
- Serine 69 was identified as a phosphorylation site, but not by Akt kinase; phosphotyrosines were absent under normal conditions.
Conclusions:
- Reversible phosphorylation of RBM5 is a key regulatory mechanism.
- RBM5 phosphorylation status influences its involvement in apoptosis modulation.
- Phosphorylation of RBM5 may play a role in tumor suppression.
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