Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.368020
Title: Characterization of inactive and stress-induced active forms of the transcription factor HSF1 : an analysis at the cellular level
Author: Vujanac, Milos
ISNI:       0000 0001 3549 386X
Awarding Body: Open University
Current Institution: Open University
Date of Award: 2000
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
In mammalian cells, the heat shock response is mediated by the heat shock transcription fact or HSF1 that forms active, DNA- binding homotrimers during temperature stress. The subcellular localization of the inactive form of HSF1 has been of gr eat interest for the potential implications in signaling in this system. I have detected the inactive form of HSF1 mostly in the nucleus of diverse mammalian cell lines. However , I have found that HSF1 is not confined to the nucleus , but continuously shuttles between the nucleus and the cytoplasm at a minimum rate of 1 molecule sec-1. A possible link of shuttling with the functional state of HSF1 is suggested by the observation that the shuttling cycle is discontinued during mild heat stress and resumes promptly during stress relaxation . A similar block of nuclear export is observed for deregulated mutants of HSF1 that trimerize at 37 °C, suggesting that the trimerization step inhibits an export activity. By mutational analysis I showed that HSF1 contains an unusual bipartite nuclear localization signal. Ongoing experiments are defining sequence requirements for nuclear export, most probably on a pathway distinct from Exportin-1 as judged from the refractoriness of nuclear export of HSF1 to Leptomycin B. I discuss a possible role of shuttling in compartment specific modifications of HSF1 or associations with co-factors.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.368020  DOI: Not available
Keywords: Heat shock; Nucleocytoplasmic transport
Share: