Abstract
Decapping protein 1a (Dcp1a) is found in P-bodies and functions in mRNA cap removal prior to its degradation. The function and binding partners of Dcp1a have been thoroughly studied, however its expression pattern is still unclear. In this study we have monitored Dcp1a expression along brain development, neuronal differentiation and during cellular stress. We found that Dcp1a is hyperphosphorylated under these physiological conditions. We followed our observations and identified the specific amino acid residues that are phosphorylated. These findings suggest a novel post-translational modification that may influence the function of Dcp1a in response to various physiological cues.
Original language | English |
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Pages (from-to) | 197-201 |
Number of pages | 5 |
Journal | FEBS Letters |
Volume | 583 |
Issue number | 1 |
DOIs | |
State | Published - 5 Jan 2009 |
Externally published | Yes |
Bibliographical note
Funding Information:This work was supported in part by Israel Science Foundation Grant 03454, by the Benoziyo Center for Neurological Diseases, and the Mario-Negri/Weizmann Foundation. I.G. is the incumbent of the Sophie and Richard S. Richards Professorial Chair in Cancer Research.
Funding
This work was supported in part by Israel Science Foundation Grant 03454, by the Benoziyo Center for Neurological Diseases, and the Mario-Negri/Weizmann Foundation. I.G. is the incumbent of the Sophie and Richard S. Richards Professorial Chair in Cancer Research.
Funders | Funder number |
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Mario-Negri/Weizmann Foundation | |
Nella and Leon Benoziyo Center for Neurological Diseases, Weizmann Institute of Science | |
Israel Science Foundation | 03454 |
Keywords
- Arsenate
- Dcp1a
- Neuronal development
- P-bodies
- Stress granules