Publication:
Degron features of the regulatory domain of squalene monooxygenase - a rate limiting enzyme in cholesterol synthesis

dc.contributor.advisor Brown, Andrew en_US
dc.contributor.advisor Yang, Hongyuan Robert en_US
dc.contributor.author Chua, Ngee Kiat en_US
dc.date.accessioned 2022-03-23T12:20:27Z
dc.date.available 2022-03-23T12:20:27Z
dc.date.issued 2020 en_US
dc.description.abstract Cholesterol is an essential lipid associated with many important biological functions. At both the cellular and physiological levels, cholesterol is acquired through two main sources. One source is uptake, while the other source is de novo cholesterol synthesis. Squalene monooxygenase (SM) is a rate-limiting enzyme of cholesterol synthesis. A few studies have suggested SM could be a promising treatment target to lower cholesterol levels in the blood and as another metabolic target in certain cancers. Thus, there is an increasing need to understand the regulation of this enzyme. One critical mode of regulation is the cholesterol-accelerated degradation of SM. This process requires the first 100 amino acids of SM (termed SM N100). The SM N100 regulatory domain represents a degron region (a degradation signal), which allows SM to be regulated by cholesterol. However, insights into cholesterol sensing by SM N100 and the mechanisms by which SM N100 confers instability were unknown. To investigate this degron, we utilised SM N100 fused to green fluorescent protein, a fusion protein which recapitulates the cholesterol-accelerated degradation of SM. Here, we have performed a series of point mutations, truncations and domain swaps based on our understanding of known degron features. We identified that an amphipathic helix (residues Gln62–Leu73) in SM N100 is required for cholesterol-accelerated degradation. We also present evidence that the cholesterol-driven disorder of the amphipathic helix lengthens the disordered region surrounding the helix and exposes a hydrophobic patch which accelerates SM N100 degradation. Attempts to identify ubiquitination sites revealed SM N100 undergoes non-canonical ubiquitination at serine residues to signal SM N100 for degradation. Finally, we identified valosin-containing protein (VCP) as a key protein which mediates the removal of the SM N100 degron from the endoplasmic reticulum into the cytosol for degradation. In summary, we have increased our understanding of the SM N100 degron architecture, furthering insights into how cholesterol sensing in the endoplasmic reticulum is coupled to protein quality control. en_US
dc.identifier.uri http://hdl.handle.net/1959.4/65592
dc.language English
dc.language.iso EN en_US
dc.publisher UNSW, Sydney en_US
dc.rights CC BY-NC-ND 3.0 en_US
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/3.0/au/ en_US
dc.subject.other Degron en_US
dc.subject.other Cholesterol en_US
dc.subject.other Cholesterol synthesis en_US
dc.subject.other Endoplasmic reticulum-associated degradation (ERAD) en_US
dc.subject.other Protein degradation en_US
dc.subject.other Squalene monooxygenase en_US
dc.subject.other Ubiquitin en_US
dc.title Degron features of the regulatory domain of squalene monooxygenase - a rate limiting enzyme in cholesterol synthesis en_US
dc.type Thesis en_US
dcterms.accessRights open access
dcterms.rightsHolder Chua, Ngee Kiat
dspace.entity.type Publication en_US
unsw.accessRights.uri https://purl.org/coar/access_right/c_abf2
unsw.description.notePublic Other Funding Scheme: Australian Research Council (ARC). Other Grant ID: DP170101178. en_US
unsw.identifier.doi https://doi.org/10.26190/unsworks/21768
unsw.relation.faculty Other UNSW
unsw.relation.originalPublicationAffiliation Chua, Ngee Kiat, UNSW en_US
unsw.relation.originalPublicationAffiliation Brown, Andrew, Biotechnology & Biomolecular Sciences, Faculty of Science, UNSW en_US
unsw.relation.originalPublicationAffiliation Yang, Hongyuan Robert, Biotechnology & Biomolecular Sciences, Faculty of Science, UNSW en_US
unsw.thesis.degreetype PhD Doctorate en_US
Files
Original bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
public version.pdf
Size:
19.22 MB
Format:
application/pdf
Description:
Resource type