Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/128389
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dc.titleACTIVATION OF ERK/MAPK SIGNALING BY BURKHOLDERIA PSEUDOMALLEI CYCLE INHIBITING FACTOR
dc.contributor.authorNG MEI YING
dc.date.accessioned2016-10-10T18:00:19Z
dc.date.available2016-10-10T18:00:19Z
dc.date.issued2016-08-03
dc.identifier.citationNG MEI YING (2016-08-03). ACTIVATION OF ERK/MAPK SIGNALING BY BURKHOLDERIA PSEUDOMALLEI CYCLE INHIBITING FACTOR. ScholarBank@NUS Repository.
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/128389
dc.description.abstractCycle inhibiting factors (Cifs) are virulence proteins secreted by the T3SS of some Gram-negative pathogenic bacteria including Burkholderia pseudomallei. Cif is known to function to deamidate Nedd8, leading to inhibition of Cullin E3 ubiquitin ligases (CRL) and consequently induction of cell cycle arrest. Here I show that Cif functions as a potent activator of MAPK/ERK signaling, and this is dependent on its deamidase activity, but independent of Cullin E3 ligase inhibition. I provide evidence that the mechanism involved is dependent on recruitment of the Grb2-SOS1 complex to the plasma membrane, and that Cif modifies the phosphorylation status of SOS1 in the CDC25-H and proline-rich domains. Since prolonged Cullin E3 ligase inhibition is known to lead to cellular apoptosis, I hypothesise that ERK activation functions to counter the pro-apoptotic effects of Cif. Indeed, I show that Cif-dependent ERK activation promotes phosphorylation of the pro-apoptotic protein Bim, thereby conferring a pro-survival signal.
dc.language.isoen
dc.subjectERK, Activation, B. pseudomallei, Cycle, Inhibiting, Factor
dc.typeThesis
dc.contributor.departmentBIOCHEMISTRY
dc.contributor.supervisorTHILO HAGEN
dc.description.degreeMaster's
dc.description.degreeconferredMASTER OF SCIENCE
dc.identifier.isiutNOT_IN_WOS
Appears in Collections:Master's Theses (Open)

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