Results 41 to 50 of about 457,413 (290)

Transformation of the mitochondrial genome

open access: yesThe International Journal of Developmental Biology, 2013
Although mitochondrial transformation is highly desirable in mammals and plants, it is only possible in two unicellular organisms, the budding yeast Saccharomyces cerevisiae and the unicellular green alga Chlamydomonas reinhardtii. Here, we give an overview of the attempts made to transform mitochondria of mammals and plants and the possible reasons ...
Véronique Larosa, Claire Remacle
openaire   +4 more sources

Origin of minicircular mitochondrial genomes in red algae

open access: yesNature Communications, 2023
Eukaryotic organelle genomes are generally of conserved size and gene content within phylogenetic groups. However, significant variation in genome structure may occur.
Yongsung Lee   +9 more
doaj   +1 more source

Multiple mitochondrial introgression events and heteroplasmy in trypanosoma cruzi revealed by Maxicircle MLST and next generation sequencing [PDF]

open access: yes, 2012
Background Mitochondrial DNA is a valuable taxonomic marker due to its relatively fast rate of evolution. In Trypanosoma cruzi, the causative agent of Chagas disease, the mitochondrial genome has a unique structural organization consisting of 20–50 ...
Andersson, B.   +9 more
core   +6 more sources

De novo assembly of the complete mitochondrial genome of sweet potato (Ipomoea batatas [L.] Lam) revealed the existence of homologous conformations generated by the repeat-mediated recombination

open access: yesBMC Plant Biology, 2022
Sweet potato (Ipomoea batatas [L.] Lam) is an important food crop, an excellent fodder crop, and a new type of industrial raw material crop. The lack of genomic resources could affect the process of industrialization of sweet potato. Few detailed reports
Zhijian Yang   +7 more
doaj   +1 more source

Analysis of two genomes from the mitochondrion-like organelle of the intestinal parasite Blastocystis: complete sequences, gene content, and genome organization. [PDF]

open access: yes, 2008
Acquisition of mitochondria by the ancestor of all living eukaryotes represented a crucial milestone in the evolution of the eukaryotic cell. Nevertheless, a number of anaerobic unicellular eukaryotes have secondarily discarded certain mitochondrial ...
Clark, C Graham, Pérez-Brocal, Vicente
core   +2 more sources

Screening for the ancient polar bear mitochondrial genome reveals low integration of mitochondrial pseudogenes (numts) in bears

open access: yesMitochondrial DNA. Part B. Resources, 2017
Phylogenetic analyses of nuclear and mitochondrial genomes indicate that polar bears captured the brown bear mitochondrial genome 160,000 years ago, leading to an extinction of the original polar bear mitochondrial genome.
Fritjof Lammers   +4 more
doaj   +1 more source

Characterization and phylogenetic analysis of the complete mitochondrial genome of Aspergillus sp. (Eurotiales: Eurotiomycetidae)

open access: yesMitochondrial DNA. Part B. Resources, 2019
In the present study, we presented the complete mitochondrial genome of Aspergillus sp. The complete mitochondrial genome of Aspergillus sp. was composed of circular DNA molecules, with a total length of 31,374 bp.
Cheng Chen   +7 more
doaj   +1 more source

The identification of mitochondrial DNA variants in glioblastoma multiforme [PDF]

open access: yes, 2014
Background: Mitochondrial DNA (mtDNA) encodes key proteins of the electron transfer chain (ETC), which produces ATP through oxidative phosphorylation (OXPHOS) and is essential for cells to perform specialised functions.
Dickinson, Adam   +8 more
core   +3 more sources

Protein sorting to mitochondria [PDF]

open access: yes, 1990
According to the endosymbiont hypothesis, mitochondria have lost the autonomy of their prokaryotic ancestors. They have to import most of their proteins from the cytosol because the mitochondrial genome codes for only a small percentage of the ...
Hartl, Franz-Ulrich, Neupert, Walter
core   +1 more source

The mitochondrial brain: From mitochondrial genome to neurodegeneration

open access: yesBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 2010
Mitochondrial DNA mutations are an important cause of neurological disease. The clinical presentation is very varied in terms of age of onset and different neurological signs and symptoms. The clinical course varies considerably but in many patients there is a progressive decline, and in some evidence of marked neurodegeneration.
Turnbull, H   +4 more
openaire   +3 more sources

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