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Mitochondrial Iron Metabolism : Study of mitoferrin in Drosophila melanogaster

Metzendorf, Christoph, 1977- (author)
Uppsala universitet,Jämförande fysiologi,Maria Lind Karlberg
Lind Karlberg, Maria, Doktor (thesis advisor)
Uppsala universitet,Jämförande fysiologi
Söderhäll, Kenneth, Professor (thesis advisor)
Uppsala universitet,Jämförande fysiologi
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Muckenthaler, Martina, Professor (opponent)
University of Heidelberg, Department of Pediatric Oncology, Hematology and Immunology, Im Neuenheimer Feld 153 69120 Heidelberg
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 (creator_code:org_t)
ISBN 9789155477226
Uppsala : Acta Universitatis Upsaliensis, 2010
English 55 s.
Series: Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, 1651-6214 ; 713
  • Doctoral thesis (other academic/artistic)
Abstract Subject headings
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  • Iron has a dualistic character. On the one hand it is essential for the life of most organisms, on the other hand it is involved in the generation of reactive oxygen species that are implicated in diseases and aging. During evolution efficient mechanisms for uptake, handling and storage of iron in a safe way have developed to keep the balance between iron availability and minimizing the hazards. In eukaryotes, mitochondria are the central organelle for “metabolizing” iron and consequently play an important role in cellular iron homeostasis. Mitoferrins are mitochondrial carrier proteins, which are involved in iron transport into mitochondria. In vertebrates two mitoferrins exist, one (mitoferrin1) of which is essential for heme synthesis during erythropoiesis, while the function of the other (mitoferrin2) is not well defined. In the fruit fly we found only one mitoferrin gene (dmfrn), which codes most likely for a functional homologueof vertebrate mitoferrin2. In Drosophila cell culture, dmfrn overexpression resulted in an overestimation of cell sensed iron levels. The signal responsible for this, is most likely a yet unidentified compound of ISC synthesis. In the cell culture system we also showed that iron chelation blocks the progression of the cell cycle in a reversible and therefore most likely controlled way. Study of different dmfrn mutants indicates a role of dmfrn during spermatogenesis and development to adulthood. As dmfrn deletion mutants are not lethal, it is likely that other lower affinity iron transporters exist. A similar conclusion has been drawn by others from the study of yeast mitoferrin homologuemutants. Rim2p/Mrs12p has recently been implicated in mitochondrial iron transport, and might be an alternative metal carrier. We identified a putative homologuein the fruit fly and found a possible link between mutants in this gene and iron. Our results emphasize the importance of the mitochondrial iron metabolism in cellular iron homeostasis. We also show for the first time, a direct connection between the mitochondrial iron metabolism and spermatogenesis. Mutants characterized and developed by us will help to study these processes in further detail and reveal the underlying mechanisms.

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

iron
Drosophila
mitochondria
mitoferrin
ferritin
spermatogenesis
cell cycle
DFO
MRS12
Cell and molecular biology
Cell- och molekylärbiologi
Biology with specialization in Comparative Physiology
Biologi med inriktning mot jämförande fysiologi

Publication and Content Type

vet (subject category)
dok (subject category)

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