نتایج جستجو برای: mt dna

تعداد نتایج: 531353  

Journal: :Nucleic acids research 1982
P Cantatore C De Benedetto G Gadaleta R Gallerani A M Kroon M Holtrop C Lanave G Pepe C Quagliariello C Saccone E Sbisa

We have determined the nucleotide sequences of thirteen rat mt tRNA genes. The features of the primary and secondary structures of these tRNAs show that those for Gln, Ser, and f-Met resemble, while those for Lys, Cys, and Trp depart strikingly from the universal type. The remainder are slightly abnormal. Among many mammalian mt DNA sequences, those of mt tRNA genes are highly conserved, thus s...

Journal: :Carcinogenesis 2005
Chi-Tai Yeh Gow-Chin Yen

The molecular mechanism of sulforaphane on the induction of metallothionein (MT) genes in HepG2 cells and the antiproliferative effects of sulforaphane were investigated in this study. Treatment of the cells with sulforaphane at non-toxicity concentration (0-20 microM) resulted in coordinate increases in the induction of MT-I and MT-II mRNA, followed by corresponding increases in MT protein exp...

Journal: :RNA 2010
Stephen J Traphagen Michael J Dimarco Margaret E Silliker

Regions of the Didymium iridis mitochondrial genome were identified with similarity to typical mitochondrial genes; however, these regions contained numerous stop codons. We used RT-PCR and DNA sequencing to determine whether, through RNA editing, these regions were transcribed into mRNAs that could encode functional proteins. Ten putative gene regions were examined: atp1, atp6, atp8, atp9, cox...

Journal: :Molecular biology and evolution 2011
Sophie Breton Donald T Stewart Sally Shepardson Richard J Trdan Arthur E Bogan Eric G Chapman Andrew J Ruminas Helen Piontkivska Walter R Hoeh

Mitochondrial (mt) function depends critically on optimal interactions between components encoded by mt and nuclear DNAs. mitochondrial DNA (mtDNA) inheritance (SMI) is thought to have evolved in animal species to maintain mito-nuclear complementarity by preventing the spread of selfish mt elements thus typically rendering mtDNA heteroplasmy evolutionarily ephemeral. Here, we show that mtDNA in...

Journal: :PLoS ONE 2008
Yasuhiro Kitazoe Hirohisa Kishino Masami Hasegawa Noriaki Nakajima Jeffrey L. Thorne Masashi Tanaka

BACKGROUND The mitochondrial (mt) gene tree of placental mammals reveals a very strong acceleration of the amino acid (AA) replacement rate and a change in AA compositional bias in the lineage leading to the higher primates (simians), in contrast to the nuclear gene tree. Whether this acceleration and compositional bias were caused by adaptive evolution at the AA level or directional mutation p...

Introduction: Effects of melatonin (MT) were comparatively examined on melanophores of isolated skin in adults and tadpole’s tailfin of a frog Rana cyanophlyctis. MT is generally considered as a potent melanophores aggregating hormone besides regulating the sleep wake cycle in vertebrates. Methods: Melanophore size index (MSI) was chosen as a recording parameter of the responses. Concentr...

Journal: :The Journal of biological chemistry 1987
K A Maguire M L Webb L C Garg S T Jacob

Nuclear extract from Morris hepatoma 3924A was fractionated by DEAE-Sephadex chromatography. The fraction eluting with 300 mM (NH4)2SO4 (DE-C) was used for transcribing cloned mouse metallothionein-I (MT-I) gene in a run-off assay. This fraction contained the majority of RNA polymerase II as well as the transcription factor(s). Accuracy of MT-I DNA transcription was confirmed by S1 nuclease map...

Journal: :Current Biology 2007
Katharina Ribbeck Tim Raemaekers Geert Carmeliet Iain W. Mattaj

The spindle apparatus is a microtubule (MT)-based machinery that attaches to and segregates the chromosomes during mitosis and meiosis. Self-organization of the spindle around chromatin involves the assembly of MTs, their attachment to the chromosomes, and their organization into a bipolar array. One regulator of spindle self-organization is RanGTP. RanGTP is generated at chromatin and activate...

Journal: :Neurobiology of Aging 2017
Katie Lunnon Aoife Keohane Ruth Pidsley Stephen Newhouse Joanna Riddoch-Contreras Elisabeth B. Thubron Matthew Devall Hikka Soininen Iwona Kłoszewska Patrizia Mecocci Magda Tsolaki Bruno Vellas Leonard Schalkwyk Richard Dobson Afshan N. Malik John Powell Simon Lovestone Angela Hodges

Although mitochondrial dysfunction is a consistent feature of Alzheimer's disease in the brain and blood, the molecular mechanisms behind these phenomena are unknown. Here we have replicated our previous findings demonstrating reduced expression of nuclear-encoded oxidative phosphorylation (OXPHOS) subunits and subunits required for the translation of mitochondrial-encoded OXPHOS genes in blood...

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