Synthesis and turnover of mitochondrial ribonucleic acid in HeLa cells: the mature ribosomal and messenger ribonucleic acid species are metabolically unstable
about
The human mitochondrial transcription termination factor (mTERF) is a multizipper protein but binds to DNA as a monomer, with evidence pointing to intramolecular leucine zipper interactions.TEFM (c17orf42) is necessary for transcription of human mtDNAThe mitochondrial transcription termination factor mTERF modulates replication pausing in human mitochondrial DNAMitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current conceptsContent of mitochondrial DNA and of three mitochondrial RNAs in developing and adult rat cerebellumThe complete nucleotide sequence of a snake (Dinodon semicarinatus) mitochondrial genome with two identical control regionsPattern of organization of human mitochondrial pseudogenes in the nuclear genomeTranscript mapping and genome annotation of ascidian mtDNA using EST dataEffects on mitochondrial transcription of manipulating mTERF protein levels in cultured human HEK293 cells.The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.A compendium of human mitochondrial gene expression machinery with links to disease.Leucine-rich pentatricopeptide-repeat containing protein regulates mitochondrial transcription.Human mitochondrial mRNAs--like members of all families, similar but differentA monomer-to-trimer transition of the human mitochondrial transcription termination factor (mTERF) is associated with a loss of in vitro activity.Functional genomic analysis of human mitochondrial RNA processing.First comparative insight into the architecture of COI mitochondrial minicircle molecules of dicyemids reveals marked inter-species variation.Coupled reductions in brain oxidative phosphorylation and synaptic function can be quantified and staged in the course of Alzheimer disease.Large functional range of steady-state levels of nuclear and mitochondrial transcripts coding for the subunits of the human mitochondrial OXPHOS system.Transcriptional requirements of the distal heavy-strand promoter of mtDNA.Hitting the brakes: termination of mitochondrial transcription.Identification of initiation sites for heavy-strand and light-strand transcription in human mitochondrial DNA.In vitro analysis of mutations causing myoclonus epilepsy with ragged-red fibers in the mitochondrial tRNA(Lys)gene: two genotypes produce similar phenotypes.Modeling RNA polymerase interaction in mitochondria of chordates.Mitochondrial DNA structure and expression in specialized subtypes of mammalian striated muscle.Mutually exclusive synthetic pathways for sea urchin mitochondrial rRNA and mRNA.Purification and characterization of human mitochondrial transcription factor 1.Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.The excised leader of human cytochrome c oxidase subunit I mRNA which contains the origin of mitochondrial DNA light-strand synthesis accumulates in mitochondria and is polyadenylated.A tridecamer DNA sequence supports human mitochondrial RNA 3'-end formation in vitroHighly efficient RNA-synthesizing system that uses isolated human mitochondria: new initiation events and in vivo-like processing patterns.MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts.Identification of the polypeptides encoded in the ATPase 6 gene and in the unassigned reading frames 1 and 3 of human mtDNA.Human mitochondrial ribosomes can switch their structural RNA composition.In vitro transcription of human mitochondrial DNA: accurate termination requires a region of DNA sequence that can function bidirectionally.Mitochondrial DNA transcription regulation and nucleoid organization.Mitochondrial transcription in mammalian cells.The RNA-Seq approach to studying the expression of mosquito mitochondrial genes.Dynamical change of mitochondrial DNA induced in the living cell by perturbing the electrochemical gradient.Tight control of respiration by NADH dehydrogenase ND5 subunit gene expression in mouse mitochondria.In vivo methylation of mtDNA reveals the dynamics of protein-mtDNA interactions.
P2860
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P2860
Synthesis and turnover of mitochondrial ribonucleic acid in HeLa cells: the mature ribosomal and messenger ribonucleic acid species are metabolically unstable
description
1981 nî lūn-bûn
@nan
1981年の論文
@ja
1981年論文
@yue
1981年論文
@zh-hant
1981年論文
@zh-hk
1981年論文
@zh-mo
1981年論文
@zh-tw
1981年论文
@wuu
1981年论文
@zh
1981年论文
@zh-cn
name
Synthesis and turnover of mito ...... ies are metabolically unstable
@en
type
label
Synthesis and turnover of mito ...... ies are metabolically unstable
@en
prefLabel
Synthesis and turnover of mito ...... ies are metabolically unstable
@en
P2860
P356
P1476
Synthesis and turnover of mito ...... ies are metabolically unstable
@en
P2093
P2860
P304
P356
10.1128/MCB.1.6.497
P407
P577
1981-06-01T00:00:00Z