Search results for "RNA editing"

showing 10 items of 21 documents

The Selaginella Genome Identifies Genetic Changes Associated with the Evolution of Vascular Plants

2011

International audience; Vascular plants appeared ~410 million years ago, then diverged into several lineages of which only two survive: the euphyllophytes (ferns and seed plants) and the lycophytes. We report here the genome sequence of the lycophyte Selaginella moellendorffii (Selaginella), the first nonseed vascular plant genome reported. By comparing gene content in evolutionarily diverse taxa, we found that the transition from a gametophyte- to a sporophyte-dominated life cycle required far fewer new genes than the transition from a nonseed vascular to a flowering plant, whereas secondary metabolic genes expanded extensively and in parallel in the lycophyte and angiosperm lineages. Sela…

0106 biological sciencesSmall RNASELAGINELLA[SDV.BC]Life Sciences [q-bio]/Cellular Biology01 natural sciencesGenome03 medical and health sciencesSelaginella moellendorffiiSelaginellaGENETIQUE VEGETALEGeneInstitut für Biochemie und Biologie030304 developmental biologyGeneticsWhole genome sequencing0303 health sciencesMultidisciplinarybiologyfungiRNAfood and beverages15. Life on landbiology.organism_classificationSELAGINELLA MOELLENDORFFIIRNA editingLYCOPHYTE010606 plant biology & botany
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2016

RNA 2'-O-methylation is one of the ubiquitous nucleotide modifications found in many RNA types from Bacteria, Archaea and Eukarya. RNAs bearing 2'-O-methylations show increased resistance to degradation and enhanced stability in helices. While the exact role of each 2'-O-Me residue remained elusive, the catalytic protein Fibrillarin (Nop1 in yeast) responsible for 2'-O-methylation in eukaryotes, is associated with human pathologies. Therefore, there is an urgent need to precisely map and quantify hundreds of 2'-O-Me residues in RNA using high-throughput technologies. Here, we develop a reliable protocol using alkaline fragmentation of total RNA coupled to a commonly used ligation approach, …

0301 basic medicineGenetics2'-O-methylation5.8S ribosomal RNARNAComputational biologyRNA integrity numberBiologyRibosomal RNA03 medical and health sciences030104 developmental biology0302 clinical medicineRNA editing030220 oncology & carcinogenesisGeneticsRNA extractionIllumina dye sequencingNucleic Acids Research
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Discovering new proteins in plant mitochondria by RNA editing simulation

2016

In plant mitochondria an essential mechanism for gene expression is RNA editing, often influencing the synthesis of functional proteins. RNA editing alters the linearity of genetic information transfer. Indeed it causes differences between RNAs and their coding DNA sequences that hinder both experimental and computational research of genes. Therefore common software tools for gene search, successfully applied to find canonical genes, often fail in discovering genes encrypted in the genome of plants. Here we propose a novel strategy useful to identify candidate coding sequences resulting from possible editing substitutions. In particular, we consider c!u substitutions leading to the creation…

0301 basic medicineGeneticsMitochondrial DNASequence analysisediting plant mitocondria simulationBiologyGenomeStop codon03 medical and health sciencesOpen reading frame030104 developmental biologyRNA editingGene expressionGene
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Normal intestinal dietary fat and cholesterol absorption, intestinal apolipoprotein B (ApoB) mRNA levels, and ApoB-48 synthesis in a hypobetalipoprot…

1997

Abstract The purpose of this study was to characterize intestinal apolipoprotein B (apoB) metabolism in subjects with familial hypobetalipoproteinemia (FHBL), where segregation analysis supports linkage to the apoB gene but no apoB truncations are present. We investigated cholesterol and fat absorption, intestinal apoB mRNA synthesis and editing, as well as apoB-48 synthesis. Plasma triglycerides (TG) and retinyl palmitate in the chylomicron fractions were analyzed after 12 hours of fasting and then repeatedly for 14 hours after ingestion of a vitamin A—containing high-fat meal. Cholesterol absorption was assessed using a dual stable-isotope method. Mean peak times and concentrations and ar…

AdultMaleVitaminmedicine.medical_specialtyApolipoprotein BEndocrinology Diabetes and Metabolismdigestive systemAbsorptionCholesterol DietaryHypobetalipoproteinemiasEatingchemistry.chemical_compoundEndocrinologyInternal medicineRetinyl palmitatemedicineHumansRNA MessengerIntestinal MucosaHypoalphalipoproteinemiaAgedApolipoproteins BMethioninebiologyCholesterolnutritional and metabolic diseasesNuclease protection assayMiddle Agedmedicine.diseaseDietary FatsLipidsEndocrinologychemistrybiology.proteinFemalelipids (amino acids peptides and proteins)RNA EditingApolipoprotein B-48ChylomicronMetabolism
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2015

The combination of Reverse Transcription (RT) and high-throughput sequencing has emerged as a powerful combination to detect modified nucleotides in RNA via analysis of either abortive RT-products or of the incorporation of mismatched dNTPs into cDNA. Here we simultaneously analyze both parameters in detail with respect to the occurrence of N-1-methyladenosine (m(1)A) in the template RNA. This naturally occurring modification is associated with structural effects, but it is also known as a mediator of antibiotic resistance in ribosomal RNA. In structural probing experiments with dimethylsulfate, m(1)A is routinely detected by RT-arrest. A specifically developed RNA-Seq protocol was tailored…

BiochemistryTranscription (biology)RNA editingGeneticsRNA polymerase IIntronRNA-dependent RNA polymeraseRNABiologyNon-coding RNAMolecular biologyPost-transcriptional modificationNucleic Acids Research
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A new triple fluorescence reporter system for discrimination of Apobec1 and Apobec3 C-to-U RNA editing activities and editing-dependent protein expre…

2021

AbstractThe human body is composed of many different cell types which communicate with each other. In particular, the brain consists of billions of neurons and non-neuronal cells which are interconnected and require tight and precise regulation of cellular processes. RNA editing is a cellular process that diversifies gene function by enzymatic deamination of cytidine or adenine. This can result in changes of protein structure and function. Altered RNA editing is becoming increasingly associated with all kind of disease, but most approaches use advanced sequencing technologies to analyze bulk material. However, it is also becoming progressively evident that changes in RNA editing have to be …

Cell typeAPOBEC1RNACytidineBiologyCell biologychemistry.chemical_compoundmedicine.anatomical_structurechemistryRNA editingmedicineNeuronGeneFunction (biology)
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The role of cell interactions in the control of RNA synthesis.

1967

CytoplasmChemistryCellular differentiation5.8S ribosomal RNACellRNAPhosphorus IsotopesCell DifferentiationRNA integrity numberNon-coding RNABiochemistry Genetics and Molecular Biology (miscellaneous)RNA polymerase IIICell biologymedicine.anatomical_structureRNA editingmedicineCentrifugation Density GradientAnimalsRNAUltracentrifugationEchinodermataBiochimica et biophysica acta
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A comparative analysis to study editing of small noncoding BC200- and Alu transcripts in brain of prion-inoculated rhesus monkeys (M. Mulatta).

2012

Small retroelements (short interspersed elements, abbreviated SINEs) are abundant in vertebrate genomes. Using RNA isolated from rhesus monkey cerebellum and buffy coat, reverse-transcription polymerase chain reaction (RT PCR) was applied to clone cDNA of BC200 and Alu RNAs. Transcripts containing Alu-SINE sequences may be subjected to extensive RNA editing by ADAR (adenosine deaminases that act on RNA) deamination. Abundance of Alu transcripts was determined with real-time RT PCR and was significantly higher than BC200 (brain cytoplasmic) in cerebellum. BC200 transcripts were absent from buffy coat cells. Availability of the rhesus genome sequence allowed the BC200 transcripts to be mapped…

DNA ComplementaryHealth Toxicology and MutagenesisMolecular Sequence DataRNA-dependent RNA polymeraseBiologyToxicologyReal-Time Polymerase Chain ReactionRNA polymerase IIICreutzfeldt-Jakob SyndromeAlu ElementsComplementary DNACerebellumAnimalsShort Interspersed Nucleotide ElementsGeneticsBase SequenceReverse Transcriptase Polymerase Chain ReactionIntronRNARNA Polymerase IIISequence Analysis DNAMolecular biologyMacaca mulattaReal-time polymerase chain reactionRNA editingADARRNARNA Small UntranslatedRNA EditingJournal of toxicology and environmental health. Part A
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Specific roles of 5′ RNA secondary structures in stabilizing transcripts in chloroplasts

2005

RNA secondary structures, e.g. stem-loops that are often found at the 5' and 3' ends of mRNAs, are in many cases known to be crucial for transcript stability but their role in prolonging the lifetime of transcripts remains elusive. In this study we show for an essential RNA-stabilizing stem-loop at the 5' end of rbcL gene transcripts in Chlamydomonas that it neither prevents ribonucleases from binding to the RNA nor impedes their movement along the RNA strand. The stem-loop has a formative function in that it mediates folding of a short sequence around its base into a specific RNA conformation, consisting of a helical and single-stranded region, i.e. the real structure required for longevit…

GeneticsFive-prime capBase SequenceRNA ChloroplastRNA StabilityRibulose-Bisphosphate CarboxylaseTrans-splicingRNA ConformationChlamydomonasMolecular Sequence DataIntronRNABiologyArticleCell biologyAntisense RNARNA silencingRNA editingGeneticsAnimalsNucleic Acid ConformationRNA Messenger5' Untranslated RegionsNucleic Acids Research
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Prion infected rhesus monkeys to study differential transcription of Alu DNA elements and editing of Alu transcripts in neuronal cells and blood cells

2012

Background  Rhesus monkeys were used as a non-human primate model to study small non-coding RNA after infection with human sporadic and variant Creutzfeldt–Jakob prions. Methods  Tissue-specific Alu DNA element transcription and editing of transcripts were assessed in neuronal – and blood cells (Buffy Coat). Results  Tissue/cell-specific transcription and editing patterns were obtained. Active Alu DNA elements belonged to several Alu DNA families, they could be located on several chromosomes, and their genomic sites were identified. Deamination by adenosine deaminase acting on RNA and apolipoprotein B editing complex was found. Conclusions  Different Alu transcription and editing programmes…

GeneticsGeneral VeterinaryApolipoprotein BRNAAlu elementSequence alignmentBuffy coatBiologyMolecular biologychemistry.chemical_compoundchemistryRNA editingTranscription (biology)biology.proteinAnimal Science and ZoologyDNAJournal of Medical Primatology
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