Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:


Written in Published in Earliest date Latest date

Sorted by

Results per page:

You searched for +publisher:"University of New Mexico" +contributor:("Parra, Karlett J."). One record found.

Search Limiters

Last 2 Years | English Only

No search limiters apply to these results.

▼ Search Limiters

University of New Mexico

1. Chan, Chun-Yuan. Yeast V-ATPase Regulation by Phosphofructokinase-1.

Degree: Biomedical Sciences Graduate Program, 2015, University of New Mexico

V-ATPase is a vacuolar (lysosome-like) ATPase-dependent proton pump necessary for maintaining pH homeostasis in the organelles of the endomembrane system. It also contributes to regulation of the cytosol pH and the extracellular pH. In specialized cells (renal intercalated cells, epididymis clear cells, and osteoclasts), V-ATPase proton transport supports urinary acidification, sperm maturation, and bone resorption. Genetic mutations of V-ATPase expressed in those tissue-specific cells cause distal renal tubular acidosis, infertility, and osteopetrosis. V-ATPases are composed of a peripheral domain (V1), which hydrolyzes ATP, and a membrane-bound domain (Vo), which transports proton. V-ATPase activity is tightly regulated in vivo by numbers of mechanisms, including reversible disassembly of the V1 and Vo domains. Glucose, the nutrient oxidized in glycolysis, modulates reversible dissociation of V-ATPase. This dissertation was aimed at understanding how subunits of phosphofructokinase-1 (α subunit and β subunit) regulate V-ATPase function. Our results showed that both subunits are important for V-ATPase activity, but β subunit displayed more significant phenotypes. Deletion of β subunit reduced glucose-dependent V1Vo reassembly and altered V-ATPase binding to its assembly factor, RAVE. We additionally investigated the mechanisms by which phosphofructokinase-1 controls V-ATPase function. We concluded that glucose-dependent V1Vo reassembly and V-ATPase function at steady state were controlled by the glycolytic flux, independently of phosphofructokinase-1. Notably, V-ATPase activation in vivo correlated with the presence of phosphoglycerate kinase at vacuolar membranes. These studies further advanced our understanding how glucose controls V-ATPase pumps in vivo. Advisors/Committee Members: Parra, Karlett J., Osley, Mary Ann, Garver, William S., Lee, Samuel A..

Subjects/Keywords: V-ATPase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Chan, C. (2015). Yeast V-ATPase Regulation by Phosphofructokinase-1. (Doctoral Dissertation). University of New Mexico. Retrieved from

Chicago Manual of Style (16th Edition):

Chan, Chun-Yuan. “Yeast V-ATPase Regulation by Phosphofructokinase-1.” 2015. Doctoral Dissertation, University of New Mexico. Accessed November 12, 2019.

MLA Handbook (7th Edition):

Chan, Chun-Yuan. “Yeast V-ATPase Regulation by Phosphofructokinase-1.” 2015. Web. 12 Nov 2019.


Chan C. Yeast V-ATPase Regulation by Phosphofructokinase-1. [Internet] [Doctoral dissertation]. University of New Mexico; 2015. [cited 2019 Nov 12]. Available from:

Council of Science Editors:

Chan C. Yeast V-ATPase Regulation by Phosphofructokinase-1. [Doctoral Dissertation]. University of New Mexico; 2015. Available from: