Search results for "codon"

showing 10 items of 196 documents

Accelerated Evolution of Fetuin-A (FETUA, also AHSG) is Driven by Positive Darwinian Selection, not GC-Biased Gene Conversion

2009

article i nfo Human Fetuin-A (FETUA, also termed AHSG) is a serum protein composed of two cystatin-like domains D1 and D2 of together 235 amino acids (aa) and an unrelated domain D3 of 114 aa. Though the protein plays a role in diverse physiological and pathological processes, comparably little is known about sequence evolution of FETUA. We therefore analyzed its molecular evolution on the basis of coding sequences of 16 primate species. Ratios of non-synonymous to synonymous substitution rates (dn/ds= ω) suggest that a previously reported acceleration of sequence evolution of exon 7, which encodes domain D3, is driven by positive selection instead of neutral evolution. Irrespective of the …

GeneticsBase Sequencealpha-2-HS-GlycoproteinNull modelGene ConversionLocus (genetics)Blood ProteinsGeneral MedicineBiologyCleavage (embryo)Protein Structure TertiaryEvolution MolecularExonMolecular evolutionGeneticsAnimalsHumansGene conversionSelection GeneticCodonSynonymous substitutionNeutral theory of molecular evolutionGene
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Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia

1997

AbstractCleidocranial dysplasia (CCD) is an autosomal-dominant condition characterized by hypoplasia/aplasia of clavicles, patent fontanelles, supernumerary teeth, short stature, and other changes in skeletal patterning and growth. In some families, the phenotype segregates with deletions resulting in heterozygous loss of CBFA1, a member of the runt family of transcription factors. In other families, insertion, deletion, and missense mutations lead to translational stop codons in the DNA binding domain or in the C-terminal transactivating region. In-frame expansion of a polyalanine stretch segregates in an affected family with brachydactyly and minor clinical findings of CCD. We conclude th…

GeneticsCleidocranial DysplasiaBiochemistry Genetics and Molecular Biology(all)RuntBrachydactylyAplasiaBiologymedicine.diseaseShort statureMolecular biologyGeneral Biochemistry Genetics and Molecular BiologyHypoplasiaStop codonmedicineMissense mutationmedicine.symptomCell
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Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia

1996

Using single strand conformational analysis we screened the complete coding sequence of the serotonin 1F (5-HT{sub 1F}) receptor gene for the presence of DNA sequence variation in a sample of 137 unrelated individuals including 45 schizophrenic patients, 46 bipolar patients, as well as 46 healthy controls. We detected only three rare sequence variants which are characterized by single base pair substitutions, namely a silent T{r_arrow}A transversion in the third position of codon 261 (encoding isoleucine), a silent C{r_arrow}T transition in the third position of codon 176 (encoding histidine), and a C{r_arrow}T transition in position -78 upstream from the start codon. The lack of significan…

GeneticsMutationCandidate geneStart codonmedicineCoding regionBiologyGene mutationTransversionmedicine.disease_causeGeneGenetics (clinical)Sequence (medicine)American Journal of Medical Genetics
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Automatic simulation of RNA editing in plants for the identification of novel putative Open Reading Frames

2017

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, intro- ducing differences between RNAs and their coding DNA sequences that hind both experimental and computational research of genes. Thus common software tools for gene search, successfully exploited to find canonic genes, often can fail in discovering genes encrypted in the genome of plants. In this work we propose a novel strategy useful to intercept candidate coding sequences resulting from some possible editing substitutions on the start and stop codons of a given input organism DNA. O…

GeneticsOpen reading framechemistry.chemical_compoundchemistryRNA editingGene expressionfood and beveragesBiologyGenomeGeneStop codonDNADNA sequencing
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Forced Retroevolution of an RNA Bacteriophage

2000

AbstractThe operator hairpin ahead of the replicase gene in RNA bacteriophage MS2 contains overlapping signals for binding the coat protein and ribosomes. Coat protein binding inhibits further translation of the gene and forms the first step in capsid formation. The hairpin sequence was partially randomized to assess the importance of this structure element for the bacteriophage and to monitor alternative solutions that would evolve on the passaging of mutant phages. The evolutionary reconstruction of the operator failed in the majority of mutants. Instead, a poor imitation developed containing only some of the recognition signals for the coat protein. Three mutants were of particular inter…

GeneticsOperator Regions GeneticBase SequencebiologyMolecular Sequence DataRNARNA-dependent RNA polymeraseRNA-Dependent RNA Polymerasebiology.organism_classificationRibosomeStop codonEvolution MolecularBacteriophageSense CodonCodon NonsenseMutagenesisProtein BiosynthesisVirologyBacteriophage MS2Nucleic Acid ConformationGeneLevivirusVirology
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A method to isolate cDNA-quality RNA from adult conifer needles and a psbA cDNA from Norway spruce

1996

Summary In order to investigate the expression of the psbA gene in damaged and undamaged Norway spruce trees ( Picea abies ) a cDNA clone encoding the D1 protein was isolated via RT-PCR. Applying a method developed by Schneiderbauer et al. (1991) with some modifications, we were able to obtain the required RNA from mature needles and successfully reverse transcribe it into cDNA. Sequence analysis of the cDNA clone revealed an open reading frame (ORF) encoding a 353 amino acid polypeptide that is highly homologous to the D1 protein sequences deduced from higher plant psbA genes. A 4 bp insertion, directly following the stop codon ochre (TAA), was found by comparison with two Pinus species, t…

GeneticsPhysiologySequence analysisfungiNucleic acid sequenceRNAPlant ScienceBiologyStop codonOpen reading frameComplementary DNARNA extractionAgronomy and Crop ScienceGeneJournal of Plant Physiology
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Differential annotation of tRNA genes with anticodon CAT in bacterial genomes.

2006

We have developed three strategies to discriminate among the three types of tRNA genes with anticodon CAT (tRNA(Ile), elongator tRNA(Met) and initiator tRNA(fMet)) in bacterial genomes. With these strategies, we have classified the tRNA genes from 234 bacterial and several organellar genomes. These sequences, in an aligned or unaligned format, may be used for the identification and annotation of tRNA (CAT) genes in other genomes. The first strategy is based on the position of the problem sequences in a phenogram (a tree-like network), the second on the minimum average number of differences against the tRNA sequences of the three types and the third on the search for the highest score value …

GeneticsRNA Transfer MetPhotobacterium profundumRNAComputational BiologySequence alignmentGenomicsBacterial genome sizeGenomicsBiologybiology.organism_classificationGenomeBacterial ProteinsEnterobacteriaceaeRNA TransferGenes BacterialTransfer RNAGeneticsAnticodonRNA Transfer IleGeneSequence AlignmentGenome BacterialTenericutesNucleic acids research
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Codon usage in the siliceous sponge Geodia cydonium: highly expressed genes in the simplest multicellular animals prefer C- and G-ending codons

2001

Among a sample of 39 Geodia cydonium (Demospongiae, Porifera) genes, with an average Gh+hC content of 51.2%, extensive structural heterogeneity and considerable variations in synonymous codon usage were found. The G + C content of coding sequences and G + C content at silent codon positions (GC3S) varied from 42.4 to 59.2% and from 35.6 to 76.5%, respectively. Correspondence analysis of 39 genes revealed that putative highly expressed genes preferentially use a limited subset of codons, which were therefore defined as preferred codons in G. cydonium. A total of 22 preferred codons for 18 amino acids with synonyms in codons were identified and they all (with one exception) end with C or G. A…

GeneticsSiliceous spongeMulticellular animalsCodon usage biasGeodia cydoniumGeneticsAnimal Science and ZoologyBiologyMolecular BiologyGeneEcology Evolution Behavior and SystematicsJournal of Zoological Systematics and Evolutionary Research
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Genome-Based Examination of Chlorophyll and Carotenoid Biosynthesis in Chlamydomonas reinhardtii    

2005

Abstract The unicellular green alga Chlamydomonas reinhardtii is a particularly important model organism for the study of photosynthesis since this alga can grow heterotrophically, and mutants in photosynthesis are therefore conditional rather than lethal. The recently developed tools for genomic analyses of this organism have allowed us to identify most of the genes required for chlorophyll and carotenoid biosynthesis and to examine their phylogenetic relationships with homologous genes from vascular plants, other algae, and cyanobacteria. Comparative genome analyses revealed some intriguing features associated with pigment biosynthesis in C. reinhardtii; in some cases, there are additiona…

GeneticsbiologyPhysiologyMutantChlamydomonas reinhardtiiPlant Sciencebiology.organism_classificationIsozymeGenomechemistry.chemical_compoundchemistryChlorophyllCodon usage biasGeneticsGeneFunction (biology)Plant Physiology
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IL-10 and TGF-β1 gene polymorphisms in Greek patients with recurrent aphthous stomatitis.

2022

Recurrent aphthous stomatitis (RAS) is one of the most frequent inflammatory disorders of the oral mucosa. Cytokines, which play an important role in RAS pathogenesis, participate directly or indirectly in normal, immunological and inflammatory processes and are secreted from cells belonging to innate and adaptive immunity as a consequence of microbial and antigenic stimuli. Gene polymorphisms in specific cytokines may predispose to RAS development. The aim of this study was the investigation and association of IL-10 and TGF-β1 gene polymorphisms with RAS.Study's cohort consisted of 60 Greek patients diagnosed with RAS, including 40 patients with minor, 10 patients with major and 10 with he…

GenotypeGreecePolymorphism Single NucleotideInterleukin-10Transforming Growth Factor beta1OtorhinolaryngologyCase-Control StudiesHumansSurgeryGenetic Predisposition to DiseaseStomatitis Aphthousrecurrent aphthous stomatitis aphthae IL-10 TGF-β gene polymorphisms oral mucosaCodonGeneral DentistryUNESCO:CIENCIAS MÉDICASMedicina oral, patologia oral y cirugia bucal
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