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Lentiviral Gene Therapy Provides Robust Protection Against Pancytopenia in an Inducible Codanin-1 Knockout Mouse Model Perry Alexandr Demsko

Dissertations & Theses @ University of Pennsylvania Available online

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Format:
Book
Thesis/Dissertation
Author/Creator:
Demsko, Perry Alexandr, author.
Contributor:
University of Pennsylvania. Cell and Molecular Biology., degree granting institution.
Language:
English
Subjects (All):
Molecular biology.
Cellular biology.
Genetics.
0307.
0379.
0369.
Local Subjects:
Molecular biology.
Cellular biology.
Genetics.
0307.
0379.
0369.
Physical Description:
1 electronic resource (103 pages)
Contained In:
Dissertations Abstracts International 86-12B
Place of Publication:
Ann Arbor : ProQuest Dissertations and Theses, 2025
Language Note:
English
Summary:
The Congenital Dyserythropoietic Anemias (CDAs) are a diverse group of rare heritable blood disorders characterized by anomalies in erythroid maturation and red blood cell production. Mechanistically varied, CDAs have lacked suitable animal models which has inhibited development of tractable therapies. CDA1a is a macrocytic CDA caused by biallelic hypofunctional mutations in Codanin-1, an enigmatic protein whose precise function has not been conclusively established. CDA1a causes morbidity and mortality though moderate to severe anemia and concurrent iron overload. We sought to rectify the lack of animal model by producing a suitable inducible Codanin-1 knockout mouse line with two disparate mechanisms of cre-based deletion, allowing for assessment of treatments for CDA1a. Using our model, we found that deletion of Codanin-1 is incompatible with life with death invariably resulting upon induction. Seeking to take advantage of this opportunity we utilized lentiviral gene therapy to restore Codanin-1 functionality, thereby establishing the ability to use gene therapy to correct CDA1a. Using our model and lentiviral system, we sought to explore human Conanin-1 mutations for better understanding of the disease pathology of CDA1a. We found that human Codanin-1 mutations do not cause disease in mice, allowing us to hypothesize about fundamental differences between human and mouse erythropoiesis. Finally, we deployed machine learning to interrogate in silico the functionality of Codanin-1 and uncovered a putative disease mechanism for CDA1a
Notes:
Source: Dissertations Abstracts International, Volume: 86-12, Section: B.
Advisors: Rivella, Stefano Committee members: Kurre, Peter; Gill, Saar; Tong, Wei; Parhiz, Hamideh
Ph.D. University of Pennsylvania 2025
Local Notes:
School code: 0175
ISBN:
9798280759688
Access Restriction:
Restricted for use by site license

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