Search results for "coding"

showing 10 items of 920 documents

Characterization of a Cu/Zn Superoxide dismutase-encoding gene region in Drosophila willistoni

1994

A Cu/Zn superoxide dismutase-encoding gene (Sod) from Drosophila willistoni was cloned and sequenced. The gene shows a typical structure for a fruit-fly Sod gene, with a coding region of 462 bp in two exons separated by a 417-bp intron. Comparison of the Sod sequences from D. willistoni and D. melanogaster suggests that these species are only remotely related. Downstream from the Sod gene, there is an ORF on the opposite strand that putatively encodes the last exon of an unidentified gene. The polyadenylation signals of the two genes are separated by only 61 bp in D. willistoni, conforming to the common picture of compact dipteran genomes.

GeneticsBase SequencebiologyPolyadenylationSuperoxide DismutaseMolecular Sequence DataIntronDNAGeneral Medicinebiology.organism_classificationMolecular biologyDrosophila virilisOpen Reading FramesExonGeneticsMelanogasterAnimalsCoding regionDrosophilaDrosophila willistoniAmino Acid SequenceGeneGene
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Structural and functional characterization of a transcription-enhancing sequence element in the rbcL gene of the Chlamydomonas chloroplast genome.

2002

The structure and function of a transcription-enhancing sequence element in the coding region of the Chlamydomonas reinhardtii rbcL gene was analyzed in Chlamydomonas chloroplast transformants in vivo. The enhancer sequence is contained within a DNA segment extending from position +108 to position +143, relative to the start site of rbcL gene transcription. The sequence remains functional when inverted or when placed 34 bp closer to or 87 bp further downstream of the basic rbcL promoter. However, it does not function from a site about 250 bp downstream of its original location. Besides promoting transcription initiation from the rbcL promoter, the element is able to augment transcription fr…

GeneticsChloroplastsbiologyRibulose-Bisphosphate CarboxylaseChlamydomonasResponse elementChlamydomonasPromoterGeneral Medicinebiology.organism_classificationGenomeEnhancer Elements GeneticTranscription (biology)GeneticsCoding regionAnimalsEnhancerPromoter Regions GeneticGenePlant ProteinsCurrent genetics
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Partial Sequence Homogenization in the 5S Multigene Families May Generate Sequence Chimeras and Spurious Results in Phylogenetic Reconstructions

2014

Multigene families have provided opportunities for evolutionary biologists to assess molecular evolution processes and phylogenetic reconstructions at deep and shallow systematic levels. However, the use of these markers is not free of technical and analytical challenges. Many evolutionary studies that used the nuclear 5S rDNA gene family rarely used contiguous 5S coding sequences due to the routine use of head-to-tail polymerase chain reaction primers that are anchored to the coding region. Moreover, the 5S coding sequences have been concatenated with independent, adjacent gene units in many studies, creating simulated chimeric genes as the raw data for evolutionary analysis. This practice…

GeneticsConcerted evolutionPhylogenetic treeMolecular Sequence DataRNA Ribosomal 5SChimeric geneBiologyEvolution MolecularPhylogeneticsMolecular evolutionEvolutionary biologyMultigene FamilyMedicagoGeneticsGene familyCoding regionGenePhylogenyEcology Evolution Behavior and SystematicsSystematic Biology
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Gene structure and function of tyrosine kinases in the marine sponge Geodia cydonium: Autapomorphic characters of Metazoa

1999

Abstract Porifera (sponges) represent the most ancient, extant metazoan phylum. They existed already prior to the ‘Cambrian Explosion’. Based on the analysis of aa sequences of informative proteins, it is highly likely that all metazoan phyla evolved from only one common ancestor (monophyletic origin). As ‘autapomorphic’ proteins which are restricted to Metazoa only, integrin receptors, receptors with scavenger receptor cysteine-rich repeats, neuronal-like receptors and protein–tyrosine kinases (PTKs) have been identified in Porifera. From the marine sponge Geodia cydonium , a receptor tyrosine kinase (RTK) has been cloned that comprises the characteristic structural topology known from oth…

GeneticsDNA ComplementarySequence Homology Amino AcidMolecular Sequence DataIntronReceptor Protein-Tyrosine KinasesGeneral MedicineBiologyExon shufflingAntibodiesIntronsReceptor tyrosine kinasePoriferaTransmembrane domainGeneticsbiology.proteinAnimalsCoding regionCalciumAmino Acid SequenceReceptorTyrosine kinaseGeneGene
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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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Molecular Evolution of the Globin Gene Cluster E in Two Distantly Related Midges, Chironomus pallidivittatus and C. thummi thummi

1998

We have studied the evolutionary dynamics of a cluster of insect globin genes by comparing the organization and sequence of the gene group in two distantly related species, Chironomus pallidivittatus and C. t. thummi. Although the general architecture of the globin gene cluster has been conserved, we have found an additional, previously undescribed gene (named Cpa F) in C. pallidivittatus which shows signs of accelerated sequence evolution at nonsynonymous codon positions. This new gene is clearly functional, as demonstrated by Northern analysis. Comparison of paralogous and orthologous genes reveals patterns of intraspecific sequence homogenization. The head-to-head-oriented globin 3 and 4…

GeneticsNonsynonymous substitutionMolecular Sequence DataStructural geneNucleic acid sequenceGenes InsectBiologyChironomidaeGlobinsEvolution MolecularMolecular evolutionMultigene FamilyGeneticsAnimalsCoding regionAmino Acid SequenceGene conversionGlobinMolecular BiologyGeneEcology Evolution Behavior and SystematicsJournal of Molecular Evolution
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162P Prevalence and spectrum analysis of germline BRCA1 and BRCA2 variants of unclear significance in HBOC Syndrome: Decoding the mysterious signals …

2021

GeneticsOncologybusiness.industryHBOC SyndromeMedicineHematologySpectrum analysisbusinessGenomeGermlineDecoding methodsAnnals of Oncology
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Abstract 4479: Unveiling the relationship between the SWI/SNF chromatin remodeling complex and noncoding RNAs

2016

Abstract Chromatin remodeling complexes are crucial for the viability of the cells due to their role in regulating interactions between DNA and histones and, therefore, modifying the accessibility of the genetic information to the transcriptional machinery. This relevance can also been seen in the SWI/SNF complex that has been associated with cancer in the last deep-sequencing efforts on tumoral genomes. BRG1 is the helicase/ATPase catalytic subunit of the SWI/SNF complex and it is frequently lost in NSCLC cell lines with a high mutation rate. In primary tumors, the loss of expression of BRG1 is also frequent, however it cannot be explained by mutations or by promoter hypermethylation. In t…

GeneticsRegulation of gene expressionCancer ResearchSmall RNABiologymedicine.disease_causeChromatin remodelingSWI/SNFHistoneOncologymicroRNAmedicinebiology.proteinCoding regionCarcinogenesisCancer Research
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Structures of two molluscan hemocyanin genes: significance for gene evolution.

2001

We present here the description of genes coding for molluscan hemocyanins. Two distantly related mollusks, Haliotis tuberculata and Octopus dofleini , were studied. The typical architecture of a molluscan hemocyanin subunit, which is a string of seven or eight globular functional units (FUs, designated a to h, about 50 kDa each), is reflected by the gene organization: a series of eight structurally related coding regions in Haliotis , corresponding to FU-a to FU-h, with seven highly variable linker introns of 174 to 3,198 bp length (all in phase 1). In Octopus seven coding regions (FU-a to FU-g) are found, separated by phase 1 introns varying in length from 100 bp to 910 bp. Both genes exh…

GeneticsSignal peptideUntranslated regionMultidisciplinarySequence Homology Amino Acidmedicine.medical_treatmentMolecular Sequence DataIntronHemocyaninDNAExonsBiologyBiological SciencesBiological EvolutionIntronsExonSpecies SpecificityMolluscaHemocyaninsmedicineCoding regionAnimalsAmino Acid SequencePeptide sequenceGeneProceedings of the National Academy of Sciences of the United States of America
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Systematic screening for mutations in the promoter and the coding region of the 5-HT1A gene.

1995

In the present study we sought to identify genetic variation in the 5-HT{sub 1A} receptor gene which through alteration of protein function or level of expression might contribute to the genetic predisposition to neuropsychiatric diseases. Genomic DNA samples from 159 unrelated subjects (including 45 schizophrenic, 46 bipolar affective, and 43 patients with Tourette`s syndrome, as well as 25 healthy controls) were investigated by single-strand conformation analysis. Overlapping PCR (polymerase chain reaction) fragments covered the whole coding sequence as well as the 5{prime} untranslated region of the 5-HT{sub 1A} gene. The region upstream to the coding sequence we investigated contains a …

GeneticsSilent mutationMutationBipolar DisorderBase SequenceMolecular Sequence DataNucleic acid sequenceBiologyGene mutationmedicine.disease_causeReceptors SerotoninGenetic variationMutationGenetic predispositionmedicineSchizophreniaCoding regionHumansGeneReceptors Serotonin 5-HT1Genetics (clinical)Polymorphism Single-Stranded ConformationalTourette SyndromeAmerican journal of medical genetics
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