• Heriot-Watt University Featured PhD Programmes
  • King Abdullah University of Science and Technology (KAUST) Featured PhD Programmes
  • University of Southampton Featured PhD Programmes
  • FindA University Ltd Featured PhD Programmes
  • University of Manchester Featured PhD Programmes
  • University College London Featured PhD Programmes
  • University of Birmingham Featured PhD Programmes
University of Leeds Featured PhD Programmes
Coventry University Featured PhD Programmes
University of Glasgow Featured PhD Programmes
Queen Mary University of London Featured PhD Programmes
FindA University Ltd Featured PhD Programmes

How does the stress-response dual-function ubiquitin ligase HACE1 capture its substrates?

This project is no longer listed in the FindAPhD
database and may not be available.

Click here to search the FindAPhD database
for PhD studentship opportunities
  • Full or part time
    Dr Stefan Bagby
    Dr CR Pudney
  • Application Deadline
    Applications accepted all year round
  • Self-Funded PhD Students Only
    Self-Funded PhD Students Only

Project Description

The central aims are to understand two potentially inter-related aspects of HACE1 structure and function: the functional relationship between the domains of HACE1, and how HACE1 captures its substrates. These aims will be achieved using a combination of structural and functional studies employing a range of molecular and cellular techniques that probe protein conformations and interactions. The techniques will include protein expression and purification, protein crystallization, mutagenesis, calorimetry, surface plasmon resonance, and ubiquitination assays.

HACE1 is a HECT-type ubiquitin ligase comprising an N-terminal ankyrin repeat region and a C-terminal HECT domain that catalyses ubiquitination, with an intervening 250 amino acid region of unknown function. As a ubiquitin ligase, HACE1 brings together ubiquitin and protein substrate and then catalyses transfer of ubiquitin to substrate, thereby acting as “molecular matchmaker and catalyst”1. Known ubiquitination substrate proteins of HACE1 include Rac1, optineurin, Rab GTPases and TRAF2. Via these substrates, plus ligase-independent protein-protein interactions, HACE1 is a key player in numerous processes, including:

1. HACE1 is a tumour suppressor involved in multiple cancers2, including prevention of the key step in breast cancer progression3 and suppression of tumourigenicity of human lung cancer cells4
2. Via Rac1 ubiquitination, HACE1 participates in host defence against pathogens, controls cell migration, and confers cellular protection against reactive oxygen species-induced damage5,6
3. HACE1 protects the heart under pressure stress by controlling autophagic clearance of protein aggregates7, and also protects against neurodegeneration by enhancing function of the oxidative stress response master regulator Nrf28, both independent of E3 ligase activity

As mentioned in 3. above, HACE1 can act as an adaptor protein, independent of its ubiquitin ligase capacity. Hence the “dual-function” in the project title. In the adaptor role of HACE1, the HECT domain is reportedly involved in protein-protein interactions8,9; this led us to hypothesise that in its ubiquitin ligase role, the HECT domain of HACE1 is involved not only in catalysing ubiquitination of substrates, but also in capturing substrates. The conventional view of substrate recognition by HECT ligases, however, is that the domains N-terminal of the HECT domain mediate substrate recognition - in HACE1, probably the ankyrin repeat domain. The student will test the validity of the conventional view of substrate recognition by HECT ligases by assessing whether both ankyrin repeat and HECT domains of HACE1, and indeed the 250-residue sequence between them, are involved in recognition of key substrates Rac1 and optineurin. Having established which parts of HACE1 are responsible for substrate capture, there is potential to undertake a multiplexed two-hybrid assay to generate HACE1 variants with increased specificity for a particular substrate.

The student will also tackle the functional relationship between the domains of HACE1, dealing with questions such as (i) Do the N- and C-terminal domains of HACE1 interact? (ii) Does substrate binding to HACE1 affect inter-domain association, and vice versa? (iii) How does ubiquitination activity differ between full length HACE1 and HECT domain alone, and how does this correlate with data on N-terminal and HECT domain interaction?

Cellular aspects of the project will involve collaboration with the groups of Josef Penninger, Scientific Director of IMBA in Vienna, and Makoto Furutani-Seiki, Yamaguchi University, Japan.

Funding Notes

We welcome all-year around applications from applicants able to self-fund and those looking to apply for external funding.


1. Berndsen, C. E. & Wolberger, C. New insights into ubiquitin E3 ligase mechanism. Nature Publishing Group 21, 301–307 (2014).
2. Zhang, L. et al. The E3 ligase HACE1 is a critical chromosome 6q21 tumor suppressor involved in multiple cancers. Nat Med 13, 1060–1069 (2007).
3. Goka, E. T. & Lippman, M. E. Loss of the E3 ubiquitin ligase HACE1 results in enhanced Rac1 signaling contributing to breast cancer progression. Oncogene 1–11 (2015). doi:10.1038/onc.2014.468
4. Liu, Z. et al. Ubiquitylation of autophagy receptor optineurin by HACE1 activates selective autophagy for tumor suppression. Cancer Cell 26, 106–120 (2014).
5. Torrino, S. et al. The E3 ubiquitin-ligase HACE1 catalyzes the ubiquitylation of active Rac1. Developmental Cell 21, 959–965 (2011).
6. Cetinbas, N. et al. Loss of the tumour suppressor Hace1 leads to ROS-dependent glutamine addiction. Oncogene 34, 4005–4010 (2015).
7. Zhang, L. et al. HACE1-dependent protein degradation provides cardiac protection in response to haemodynamic stress. Nature Comm. 5, 1–14 (2014).
8. Rotblat, B. et al. HACE1 reduces oxidative stress and mutant Huntingtin toxicity by promoting the NRF2 response. Proc. Natl. Acad. Sci. U.S.A. 111, 3032–3037 neurin by HACE1 activates selective autophagy for tumor suppression. Cancer Cell 26, 106–120 (2014).
9. Zhao, J., Zhang, Z., Vucetic, Z., Soprano, K. J. & Soprano, D. R. HACE1: A novel repressor of RAR transcriptional activity. J. Cell. Biochem. 107, 482–493 (2009).

How good is research at University of Bath in Biological Sciences?

FTE Category A staff submitted: 24.50

Research output data provided by the Research Excellence Framework (REF)

Click here to see the results for all UK universities
Share this page:

Cookie Policy    X