Reyna Sara Quintero-Barceinas
ELK-1 ubiquitination status and transcriptional activity are modulated independently of F-Box protein FBXO25
Quintero-Barceinas, Reyna Sara; Gehringer, Franziska; Ducker, Charles; Saxton, Janice; Shaw, Peter E.
Authors
Franziska Gehringer
CHARLES DUCKER CHARLES.DUCKER1@NOTTINGHAM.AC.UK
Research Fellow
Janice Saxton
Peter E. Shaw
Abstract
The mitogen-responsive, ETS-domain transcription factor ELK-1 stimulates the expression of immediate early genes at the onset of the cell cycle and participates in early developmental programming. ELK-1 is subject to multiple levels of posttranslational control, including phosphorylation, SUMOylation, and ubiquitination. Recently, removal of monoubiquitin from the ELK-1 ETS domain by the Ubiquitin Specific Protease USP17 was shown to augment ELK-1 transcriptional activity and promote cell proliferation. Here we have used coimmunoprecipitation experiments, protein turnover and ubiquitination assays, RNA-interference and gene expression analyses to examine the possibility that USP17 acts antagonistically with the F-box protein FBXO25, an E3 ubiquitin ligase previously shown to promote ELK-1 ubiquitination and degradation. Our data confirm that FBXO25 and ELK-1 interact in HEK293T cells and that FBXO25 is active toward Hand1 and HAX1, two of its other candidate substrates. However, our data indicate that FBXO25 neither promotes ubiquitination of ELK-1 nor impacts on its transcriptional activity and suggest that an E3 ubiquitin ligase other than FBXO25 regulates ELK-1 ubiquitination and function.
Citation
Quintero-Barceinas, R. S., Gehringer, F., Ducker, C., Saxton, J., & Shaw, P. E. (2021). ELK-1 ubiquitination status and transcriptional activity are modulated independently of F-Box protein FBXO25. Journal of Biological Chemistry, 296, Article 100214. https://doi.org/10.1074/jbc.ra120.014616
Journal Article Type | Article |
---|---|
Acceptance Date | Dec 11, 2020 |
Online Publication Date | Jan 4, 2021 |
Publication Date | 2021 |
Deposit Date | Feb 4, 2021 |
Publicly Available Date | Feb 4, 2021 |
Journal | Journal of Biological Chemistry |
Print ISSN | 0021-9258 |
Electronic ISSN | 1083-351X |
Publisher | American Society for Biochemistry and Molecular Biology |
Peer Reviewed | Peer Reviewed |
Volume | 296 |
Article Number | 100214 |
DOI | https://doi.org/10.1074/jbc.ra120.014616 |
Keywords | gene regulation; ETS transcription factor family; ubiquitin ligase; cell proliferation; development; ubiquitin-specific protease 17 (USP17) |
Public URL | https://nottingham-repository.worktribe.com/output/5291909 |
Publisher URL | https://www.sciencedirect.com/science/article/pii/S0021925820002100 |
Additional Information | This article is maintained by: Elsevier; Article Title: ELK-1 ubiquitination status and transcriptional activity are modulated independently of F-Box protein FBXO25; Journal Title: Journal of Biological Chemistry; CrossRef DOI link to publisher maintained version: https://doi.org/10.1074/jbc.RA120.014616; Content Type: article; Copyright: © 2020 The Authors. Published by Elsevier Inc on behalf of American Society for Biochemistry and Molecular Biology. |
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