Deubiquitination of ELK-1 by USP17 regulates its transcriptional potency and cell proliferation

Ducker, Charles (2018) Deubiquitination of ELK-1 by USP17 regulates its transcriptional potency and cell proliferation. PhD thesis, University of Nottingham.

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The transcription factor ELK-1 is associated with numerous cellular processes, notably in cell proliferation and lineage determination. ELK-1 forms a ternary complex with a dimer of Serum Response Factor at Serum Response Elements associated with immediate-early genes, such as CFOS. Following mitogen-stimulated activation of the ERK cascade, ELK-1 is phosphorylated to mediate transcriptional activation of its target genes.

Further to phosphorylation, ELK-1 is covalently modified post-translationally with both monoubiquitin and polyubiquitin chains. This study sought to understand the functional significance and regulation of ELK-1 ubiquitination. Sites of ubiquitination of ELK-1 ectopically expressed in HEK293T cells were mapped and screened for the signature diglycine motif associated with ubiquitinated tryptic peptides using liquid chromatography - tandem mass spectrometry (LC-MS/MS). This revealed that lysine residues within the amino-terminal DNA-binding domain of ELK-1 are monoubiquitinated, including those involved in DNA binding.

Ubiquitination is reversed through the action of deubiquitinating enzymes (DUBs), which are target specific, allowing dynamic control over the protein modification state. USP17, one of several candidate DUBs, was shown to deubiquitinate ELK-1 when ectopically expressed in HEK293T cells. This was reversed when USP17 expression was knocked down, which also downregulated transcription of ELK-1 responsive genes CFOS and EGR1. Furthermore, USP17 knock-down in HEK293T cells reduced cell proliferation, an effect that was partially rescued by expression of a hypo-ubiquitinated ELK-1 mutant. Taken together, these results reveal monoubiquitination to be a key regulator of ELK-1 transcriptional potency and mitogen-driven proliferation.

Item Type: Thesis (University of Nottingham only) (PhD)
Supervisors: Layfield, Robert
Shaw, Peter
Subjects: Q Science > QP Physiology > QP501 Animal biochemistry
Faculties/Schools: UK Campuses > Faculty of Medicine and Health Sciences > School of Life Sciences
Item ID: 48595
Depositing User: Ducker, Charles
Date Deposited: 12 Jul 2018 04:40
Last Modified: 08 May 2020 09:00

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