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dc.contributor.advisorLangeland, James A., 1964-
dc.contributor.advisorXu, Hong
dc.contributor.authorArnoldi, Ashley A.
dc.date.accessioned2012-02-24T17:21:22Z
dc.date.available2012-02-24T17:21:22Z
dc.date.issued2012
dc.identifier.urihttp://hdl.handle.net/10920/25198
dc.descriptionv, 32 p.en_US
dc.description.abstractMitochondria are essential organelles for most eukaryotic organisms, as they supply the majority of energy to the cell. Mitochondria are unique from the rest of the cell in that they contain their own genome and are inherited solely from the mother. During oogenesis, many proteins and RNAs, as well as mitochondria, accumulate in the cytoplasm of the egg to be used during initial development of the embryo. However, during embryogenesis, regulation of replication, transcription, and translation of the mitochondrial genome, mtDNA, remains unknown. The small circular mitochondrial genome encodes for only 13 polypeptides, while the remaining approximately 1500 mitochondrial proteins are nuclear encoded. Included among these are the proteins involved in replication, transcription, and translation of mtDNA. This dependence on nuclear proteins for mitochondrial biogenesis led to the first hypothesis that production of mitochondrial DNA, mRNA, and protein is coupled to changes in nuclear DNA levels during development. A second hypothesis takes into account the relationship between cell size and mitochondrial levels, with larger cells tending to require more energy and therefore mitochondrial activity. Without cell growth then, mitochondrial DNA, mRNA, and protein levels should remain constant. Analyses of mitochondrial DNA and mRNA were conducted using qPCR techniques while protein levels were analyzed with Western blotting of samples from Drosophila melanogaster embryos at different stages of development. Results indicate that nuclear DNA levels may influence mtDNA replication, while cell size may contribute to the regulation of mitochondrial DNA transcription and translation. Future work should confirm these findings and explore other possible factors involved in regulation of mitochondrial biogenesis.en_US
dc.description.sponsorshipNational Heart, Lunch, and Blood Institute. National Institutes of Health. Bethesda, Maryland.en_US
dc.format.mimetypeapplication/pdf
dc.language.isoen_USen_US
dc.publisherKalamazoo Collegeen_US
dc.relation.ispartofKalamazoo College Biology Senior Individualized Projects Collection
dc.relation.ispartofseriesSenior Individualized Projects. Biology;
dc.rightsU.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder.
dc.titleInvestigating Mitochondrial Biogenesis During Drosophila melanogaster Embryogenesisen_US
dc.typeThesisen_US
KCollege.Access.ContactIf you are not a current Kalamazoo College student, faculty, or staff member, email dspace@kzoo.edu to request access to this thesis.


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  • Biology Senior Individualized Projects [1520]
    This collection includes Senior Individualized Projects (SIP's) completed in the Biology Department. Abstracts are generally available to the public, but PDF files are available only to current Kalamazoo College students, faculty, and staff.

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