Subcellular partitioning of MRP RNA assessed by ultrastructural and biochemical analysis. - Wikidata - awgldk - TriplyDB

Subcellular partitioning of MRP RNA assessed by ultrastructural and biochemical analysis.

Subcellular partitioning of MRP RNA assessed by ultrastructural and biochemical analysis.

http://www.wikidata.org/entity/Q36233859

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Evolutionary comparison provides evidence for pathogenicity of RMRP mutations.RNase MRP and the RNA processing cascade in the eukaryotic ancestor LRP130, a pentatricopeptide motif protein with a noncanonical RNA-binding domain, is bound in vivo to mitochondrial and nuclear RNAs hPop1: an autoantigenic protein subunit shared by the human RNase P and RNase MRP ribonucleoproteins Autoantigenic properties of some protein subunits of catalytically active complexes of human ribonuclease P RNA-protein interactions in the human RNase MRP ribonucleoprotein complex.Basic domains target protein subunits of the RNase MRP complex to the nucleolus independently of complex association Interactions between subunits of Saccharomyces cerevisiae RNase MRP support a conserved eukaryotic RNase P/MRP architecture.Global identification of new substrates for the yeast endoribonuclease, RNase mitochondrial RNA processing (MRP)Characterization of a unique protein component of yeast RNase MRP: an RNA-binding protein with a zinc-cluster domain.Mutagenesis of SNM1, which encodes a protein component of the yeast RNase MRP, reveals a role for this ribonucleoprotein endoribonuclease in plasmid segregation.Eukaryotic ribonuclease P: a plurality of ribonucleoprotein enzymes RNase MRP RNA and human genetic diseases Nuclear outsourcing of RNA interference components to human mitochondria 3' terminal diversity of MRP RNA and other human noncoding RNAs revealed by deep sequencing.Yeast as a model for human mtDNA replication.The RNase P associated with HeLa cell mitochondria contains an essential RNA component identical in sequence to that of the nuclear RNase P.Worldwide mutation spectrum in cartilage-hair hypoplasia: ancient founder origin of the major70A-->G mutation of the untranslated RMRP.Functional characterization of the Drosophila MRP (mitochondrial RNA processing) RNA gene Towards mitochondrial gene therapy: DQAsomes as a strategy.Functional equivalence of hairpins in the RNA subunits of RNase MRP and RNase P in Saccharomyces cerevisiae Characterization of MRP RNA-protein interactions within the perinucleolar compartment.Autoantibodies against small nucleolar ribonucleoprotein complexes and their clinical associations.A nuclear function for RNase MRP.RNase MRP cleaves pre-tRNASer-Met in the tRNA maturation pathway.A functional dominant mutation in Schizosaccharomyces pombe RNase MRP RNA affects nuclear RNA processing and requires the mitochondrial-associated nuclear mutation ptp1-1 for viability Dynamic localization of RNase MRP RNA in the nucleolus observed by fluorescent RNA cytochemistry in living cells.Two distinct structural elements of 5S rRNA are needed for its import into human mitochondria Localization of HIV RNA in mitochondria of infected cells: potential role in cytopathogenicity A persistent RNA-DNA hybrid is formed during transcription at a phylogenetically conserved mitochondrial DNA sequence.Evidence for the presence of 5S rRNA in mammalian mitochondria.Association of RNase mitochondrial RNA processing enzyme with ribonuclease P in higher ordered structures in the nucleolus: a possible coordinate role in ribosome biogenesis.Small RNAs derived from lncRNA RNase MRP have gene-silencing activity relevant to human cartilage-hair hypoplasia.LncRNA-RMRP promotes carcinogenesis by acting as a miR-206 sponge and is used as a novel biomarker for gastric cancer.tRNAs are imported into mitochondria of Trypanosoma brucei independently of their genomic context and genetic origin Non-coding RNAs: the dark side of nuclear-mitochondrial communication.Evidence for import of a lysyl-tRNA into marsupial mitochondria.Comparison of preribosomal RNA processing pathways in yeast, plant and human cells - focus on coordinated action of endo- and exoribonucleases.Wobble modification differences and subcellular localization of tRNAs in Leishmania tarentolae: implication for tRNA sorting mechanism.Molecular structure and function of autoantigens in systemic sclerosis.

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P2860

Subcellular partitioning of MRP RNA assessed by ultrastructural and biochemical analysis.

http://www.wikidata.org/entity/Q36233859

description

1994 nî lūn-bûn

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1994年论文

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Subcellular partitioning of MRP RNA assessed by ultrastructural and biochemical analysis.

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Subcellular partitioning of MRP RNA assessed by ultrastructural and biochemical analysis.

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type

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Subcellular partitioning of MRP RNA assessed by ultrastructural and biochemical analysis.

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Subcellular partitioning of MRP RNA assessed by ultrastructural and biochemical analysis.

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Subcellular partitioning of MRP RNA assessed by ultrastructural and biochemical analysis.

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Subcellular partitioning of MRP RNA assessed by ultrastructural and biochemical analysis.

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Subcellular partitioning of MRP RNA assessed by ultrastructural and biochemical analysis.

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C S Smagula

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H K Hagler

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J A Richardson

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K Li

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M Gonzalez

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R S Williams

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W J Parsons

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P2860

Human genes and pseudogenes for the 7SL RNA component of signal recognition particle

A novel endoribonuclease cleaves at a priming site of mouse mitochondrial DNA replication

Sequence and organization of the human mitochondrial genome

Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei

RNase P activity in the mitochondria of Saccharomyces cerevisiae depends on both mitochondrion and nucleus-encoded components.

Characterization of human MRP/Th RNA and its nuclear gene: full length MRP/Th RNA is an active endoribonuclease when assembled as an RNP

Evidence that vault ribonucleoprotein particles localize to the nuclear pore complex

Similarity of human mitochondrial transcription factor 1 to high mobility group proteins

The gene for the RNA component of the mitochondrial RNA-processing endoribonuclease is located on human chromosome 9p and on mouse chromosome 4

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

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ribonuclease MRP complex

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2119977

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