Search results for " genomi"

showing 10 items of 572 documents

Functional analysis of 12 ORFs fromSaccharomyces cerevisiae chromosome II

1999

Twelve different ORFs have been deleted from the right arm of Saccharomyces cerevisiae chromosome II; namely YBR193c, YBR194w, YBR197c, YBR198c, YBR201w, YBR203w, YBR207w, YBR209w, YBR210w, YBR211c, YBR217w and YBR228w. Tetrad analysis of heterozygous deletant strains revealed that YBR193c, YBR198c and YBR211c are essential genes for vegetative growth. No effects were detected in any of the haploid deletion mutants for the rest of the ORFs with respect to growth, gross morphology or mating.

GeneticsFunctional analysisbiologySaccharomyces cerevisiaeChromosomeBioengineeringbiology.organism_classificationApplied Microbiology and BiotechnologyBiochemistryGeneticsORFSPloidyTetradGeneFunctional genomicsBiotechnologyYeast
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Epistasis between new mutations and genetic background and a test of genetic canalization.

2001

The importance for fitness of epistatic interactions among mutations is poorly known, yet epistasis can exert important effects on the dynamics of evolving populations. We showed previously that epistatic interactions are common between pairs of random insertion mutations in the bacterium Escherichia coli. In this paper, we examine interactions between these mutations and other mutations by transducing each of twelve insertion mutations into two genetic backgrounds, one ancestral and the other having evolved in, and adapted to, a defined laboratory environment for 10,000 generations. To assess the effect of the mutation on fitness, we allowed each mutant to compete against its unmutated cou…

GeneticsMutationGenotypeMutantEpistasis and functional genomicsEpistasis GeneticBiologymedicine.disease_causePositive correlationEvolution MolecularMutagenesis InsertionalEvolutionary biologyTransduction GeneticMutationmedicineGeneticsEscherichia coliEpistasisGeneral Agricultural and Biological SciencesEscherichia coliEcology Evolution Behavior and SystematicsEvolution; international journal of organic evolution
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SLC23A2 Gene Variation, Vitamin C Levels, and Glaucoma

2014

Abstract Primary open-angle glaucoma (POAG) is a multifactorial disease in which both genetic and environmental factors are involved. Among the environmental factors associated with POAG, nutritional factors are particularly important since nutrition is essential for maintaining good health. Researchers can study the interactions between nutrition and genes by means of nutritional genomics, but nutrigenomics studies regarding eye diseases are very scarce. This research group recently published one of the first studies on nutrigenomics in POAG. It was found that the rs1279683 polymorphism in the SLC23A2 gene, which encodes a vitamin C transporter, is associated with a higher risk of POAG. Si…

GeneticsNutritional genomicsgenetic structuresGlaucomaDiseaseBiologyBioinformaticsmedicine.diseaseeye diseasesNutrigeneticsNutrigenomicsPolymorphism (computer science)Genotypemedicinesense organsRisk factor
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Epistasis and the Adaptability of an RNA Virus

2005

Abstract We have explored the patterns of fitness recovery in the vesicular stomatitis RNA virus. We show that, in our experimental setting, reversions to the wild-type genotype were rare and fitness recovery was at least partially driven by compensatory mutations. We compared compensatory adaptation for genotypes carrying (1) mutations with varying deleterious fitness effects, (2) one or two deleterious mutations, and (3) pairs of mutations showing differences in the strength and sign of epistasis. In all cases, we found that the rate of fitness recovery and the proportion of reversions were positively affected by population size. Additionally, we observed that mutations with large fitness…

GeneticsPopulation DensityMutationAnalysis of VarianceGenotypeEpistasis and functional genomicsAdaptation BiologicalRNA virusEpistasis GeneticSequence Analysis DNAViral Plaque AssayBiologyInvestigationsbiology.organism_classificationmedicine.disease_causeVesicular stomatitis Indiana virusEvolution MolecularMutational meltdownGenotypeMutationGeneticsmedicineEpistasisMutation–selection balanceAdaptation
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Decreasing the Number of Gaps in the Draft Assembly of theMannheimia Haemolytica M7/2 Genome Sequence

2009

GeneticsWhole genome sequencingComparative genomicsmedicine.medical_specialtyShipping feverMANNHEIMIA HAEMOLYTICACattle DiseasesBiologymedicine.diseaselaw.inventionlawMolecular geneticsmedicineGenePolymerase chain reaction
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Aneuploidy and Ethanol Tolerance in

2018

Response to environmental stresses is a key factor for microbial organism growth. One of the major stresses for yeasts in fermentative environments is ethanol. Saccharomyces cerevisiae is the most tolerant species in its genus, but intraspecific ethanol-tolerance variation exists. Although, much effort has been done in the last years to discover evolutionary paths to improve ethanol tolerance, this phenotype is still hardly understood. Here, we selected five strains with different ethanol tolerances, and used comparative genomics to determine the main factors that can explain these phenotypic differences. Surprisingly, the main genomic feature, shared only by the highest ethanol-tolerant st…

Geneticschromosome IIIwine yeastsSaccharomyces cerevisiaeaneuploidycomparative genomicsethanol toleranceOriginal ResearchFrontiers in genetics
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Molecular biology approaches utilized in preimplantation genetics: real-time PCR, microarrays, next-generation sequencing, karyomapping, and others

2020

Abstract Over the past few decades the development of new molecular technologies has revolutionized diagnosis in the reproductive medicine field, with the evaluation of the two main factors involved in a successful pregnancy: the embryo and the endometrium. The detection of genetically abnormal embryos, as well as the identification of an optimum endometrium using transcriptomics have become a priority in assisted reproductive treatments to increase pregnancy rates. This chapter provides an overview of the molecular techniques currently employed in assisted reproduction for embryo evaluation such as preimplantation genetic testing karyotyping, fluorescence in situ hybridization, polymerase …

Geneticsmedicine.diagnostic_testBiologyDNA sequencinglaw.inventionTranscriptomeReal-time polymerase chain reactionlawmedicineDNA microarrayPolymerase chain reactionComparative genomic hybridizationFluorescence in situ hybridizationGenetic testing
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Novel insights in the genetics of HCC recurrence and advances in transcriptomic data integration.

2011

Background & Aims: In approximately 70% of patients with hepatocellular carcinoma (HCC) treated by resection or ablation, disease recurs within 5 years. Although gene expression signatures have been associated with outcome, there is no method to predict recurrence based on combined clinical, pathology, and genomic data (from tumor and cirrhotic tissue). We evaluated gene expression signatures associated with outcome in a large cohort of patients with early stage (Barcelona-Clinic Liver Cancer 0/A), single-nodule HCC and heterogeneity of signatures within tumor tissues. Methods:We assessed 287 HCC patients undergoing resection and tested genome-wide expression platforms using tumor (n = 287)…

Geneticsmedicine.medical_specialtyHepatologyHepatocellular carcinomaBioinformaticsComparative genomicsHazard ratioHepatologyBiologymedicine.diseaseArticleTranscriptomeComparative transcriptomicsInternal medicineHepatocellular carcinomaGene expressionmedicineGeneticsStage (cooking)Progenitor cellHCCLiver cancerTranscriptomeJournal of hepatology
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Search forReCQL4mutations in 39 patients genotyped for suspected Rothmund-Thomson/Baller-Gerold syndromes

2014

Three overlapping conditions, namely Rothmund-Thomson (RTS), Baller-Gerold (BGS) and RAPADILINO syndromes, have been attributed to RECQL4 mutations. Differential diagnoses depend on the clinical presentation, but the numbers of known genes remain low, leading to the widespread prescription of RECQL4 sequencing. The aim of our study was therefore to determine the best clinical indicators for the presence of RECQL4 mutations in a series of 39 patients referred for RECQL4 molecular analysis and belonging to the RTS (27 cases) and BGS (12 cases) spectrum. One or two deleterious RECQL4 mutations were found in 10/27 patients referred for RTS diagnosis. Clinical and molecular reevaluation led to a…

Geneticsmedicine.medical_specialtybusiness.industryPoikilodermaConsanguinityBaller–Gerold syndromemedicine.diseaseDermatology3. Good healthHereditary sclerosing poikilodermaGenotypeGeneticsmedicinebusinessRothmund–Thomson syndromeGenetics (clinical)Comparative genomic hybridizationPorokeratosisClinical Genetics
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Comparative Genomics of Serratia spp.: Two Paths towards Endosymbiotic Life

2012

Symbiosis is a widespread phenomenon in nature, in which insects show a great number of these associations. Buchnera aphidicola, the obligate endosymbiont of aphids, coexists in some species with another intracellular bacterium, Serratia symbiotica. Of particular interest is the case of the cedar aphid Cinara cedri, where B. aphidicola BCc and S. symbiotica SCc need each other to fulfil their symbiotic role with the insect. Moreover, various features seem to indicate that S. symbiotica SCc is closer to an obligate endosymbiont than to other facultative S. symbiotica, such as the one described for the aphid Acirthosyphon pisum (S. symbiotica SAp). This work is based on the comparative genomi…

Genome evolutionEvolutionary ProcessesSerratialcsh:MedicineGenomicsBiologyForms of EvolutionGenomeMicrobiologyEvolution Molecular03 medical and health sciencesBuchneraPhylogeneticsAnimalslcsh:ScienceSymbiosisGenome sizeBiologyGenome EvolutionPhylogeny030304 developmental biologyGeneticsComparative genomics0303 health sciencesEvolutionary BiologyMultidisciplinaryObligate030306 microbiologylcsh:RComputational BiologyGenomicsComparative Genomicsbiology.organism_classificationAphidsMicrobial Evolutionlcsh:QBuchneraGenome BacterialResearch ArticleCoevolutionPLoS ONE
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