Link to the University of Pittsburgh Homepage
Link to the University Library System Homepage Link to the Contact Us Form

Mitochondrial Allotopic Gene Therapy Approaches Using a Drosophila Model with an Endogenous ATP6 Mutation

Chiu, Wai Kan (2014) Mitochondrial Allotopic Gene Therapy Approaches Using a Drosophila Model with an Endogenous ATP6 Mutation. Doctoral Dissertation, University of Pittsburgh. (Unpublished)

[img] PDF (ChiuWK_ETD_Final)
Primary Text
Restricted to University of Pittsburgh users only until 18 March 2019.

Download (2MB) | Request a Copy


Mitochondrial Encephalomyopathies are a group of disorders with common symptoms such as neurological, cardiac, and muscular dysfunctions. Mutations in ATP6, a protein-coding gene in the mitochondria genome, can lead to NARP, MILS, or FBSN diseases. ATP6 encodes a protein subunit of the ATP synthase, also known as complex V. Currently, there is no cure for patients with ATP6 mutations, and pharmacotherapies provide limited benefits. Because manipulation of mitochondrial genome is extremely difficult, allotopic expression of ATP6 – specifically, expressing the mitochondrially-encoded ATP6 gene in the nucleus – has been championed as a potential gene therapy strategy. Efficacies of allotopic rescue in in vitro systems have been controversial, with some studies showing the restoration of ATP synthase activity and some showing the lack of any rescue effects. We have isolated a Drosophila strain with a missense mutation in ATP6. The phenotypes of this mutant ATP6 strain have been characterized and are very similar to those of human patients, making it an excellent model for diseases caused by ATP6 mutation. The overarching goal of this dissertation is to import nucleus-encoded ATP6 protein into the mitochondria. This work examines the efficacies of multiple strategies in enhancing the functional outcomes of the first animal model with a stable and endogenous ATP6 mutation and shows that algal ATP6 protein provides the most promising rescue results.


Social Networking:
Share |


Item Type: University of Pittsburgh ETD
Status: Unpublished
CreatorsEmailPitt UsernameORCID
Chiu, Wai
ETD Committee:
TitleMemberEmail AddressPitt UsernameORCID
Thesis AdvisorPalladino, Michael Jmjp44@pitt.eduMJP44
Committee ChairGalbiati, Ferrucciofeg5@pitt.eduFEG5
Committee MemberDeFranco, Donalddod1@pitt.eduDOD1
Committee MemberZhang, Linzhanglx@upmc.eduLIZ22
Committee MemberGreenamyre, J. Timothyjgreena@pitt.eduJGREENA
Date: 18 March 2014
Date Type: Publication
Defense Date: 7 March 2014
Approval Date: 18 March 2014
Submission Date: 14 March 2014
Access Restriction: 5 year -- Restrict access to University of Pittsburgh for a period of 5 years.
Number of Pages: 171
Institution: University of Pittsburgh
Schools and Programs: School of Medicine > Molecular Pharmacology
Degree: PhD - Doctor of Philosophy
Thesis Type: Doctoral Dissertation
Refereed: Yes
Uncontrolled Keywords: Drosophila, ATP6, Mitochondria, NARP, MILS, Allotopic Gene Therapy
Date Deposited: 18 Mar 2014 18:13
Last Modified: 19 Dec 2016 14:41


Monthly Views for the past 3 years

Plum Analytics

Actions (login required)

View Item View Item