Search results for "Complement"

showing 10 items of 2113 documents

A genome-scale study of metabolic complementation in endosymbiotic consortia: the case of the cedar aphid

2017

AbstractBacterial endosymbionts and their insect hosts establish an intimate metabolic relationship. Bacteria offer a variety of essential nutrients to their hosts, whereas insect cells provide the necessary sources of matter and energy to their tiny metabolic allies. These nutritional complementations sustain themselves on a diversity of metabolite exchanges between the cell host and the reduced yet highly specialized bacterial metabolism –which, for instance, overproduces a small set of essential amino acids and vitamins. A well-known case of metabolic complementation is provided by the cedar aphidCinara cedrithat harbors two co-primary endosymbionts,Buchnera aphidicolaBCc andCa.Serratia …

Genetics0303 health sciences030306 microbiologySystems biologyIn silicoMicrobial metabolismMetabolic networkBiologybiochemical phenomena metabolism and nutritionbiology.organism_classificationGenomeComplementation03 medical and health sciencesMetabolic pathwayBuchnera030304 developmental biology
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A NEW PCR-BASED TYPING OF THE RODGERS AND CHIDO ANTIGENIC DETERMINANTS OF THE FOURTH COMPONENT OF HUMAN COMPLEMEMT

1994

The Rodgers (Rg) and Chido (Ch) blood groups are antigenic determinants of the fourth component of human complement C4. They are associated with the two isotypes of C4, C4A and C4B, respectively. They serve as markers to distinguish C4A from C4B as well as for the definition of subtypes of common and rare allotypes. As an alternative to the serological typing method using human alloantisera, a PCR typing procedure with sequence-specific primers (PCR-SSP) was designed. The method was tested on selected DNA samples from individuals with well-defined C4 allotypes. No false-positive or false-negative typing results were obtained and all the determinant combinations could be distinguished. The P…

GeneticsAntigenicityGenotypeImmunologyC4ABiologyPolymerase Chain ReactionIsotypelaw.inventionBlood Grouping and CrossmatchinglawGenotypeBlood Group AntigensComplement C4bGeneticsHumansTypingAlleleGenotypingAllelesPolymerase chain reactionDNA PrimersEuropean Journal of Immunogenetics
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Determination of the Core of a Minimal Bacterial Gene Set

2004

SUMMARY The availability of a large number of complete genome sequences raises the question of how many genes are essential for cellular life. Trying to reconstruct the core of the protein-coding gene set for a hypothetical minimal bacterial cell, we have performed a computational comparative analysis of eight bacterial genomes. Six of the analyzed genomes are very small due to a dramatic genome size reduction process, while the other two, corresponding to free-living relatives, are larger. The available data from several systematic experimental approaches to define all the essential genes in some completely sequenced bacterial genomes were also considered, and a reconstruction of a minima…

GeneticsBacteriaComputational BiologyReviewComputational biologyBacterial genome sizeBiologyMicrobiologyGenomeSet (abstract data type)Core (game theory)Infectious DiseasesBacterial ProteinsGenes BacterialMinimal genomeMolecular BiologyGeneGenome sizeGenome BacterialComplement (set theory)Microbiology and Molecular Biology Reviews
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The human complement component C8B gene: structure and phylogenetic relationship

1993

The eighth component of human complement (C8) is a serum protein that consists of three chains (alpha, beta and gamma), encoded by three separate genes, viz., C8A, C8B, and C8G. In serum, the beta-subunit is non-covalently bound to the disulfide-linked alpha-gamma subunit. Using a full-length C8 beta cDNA probe, we isolated several clones from human genomic lambda DNA libraries. Four lambda clones covering the complete cDNA sequence were characterized by TaqI restriction mapping and were "shotgun" subcloned into M13. C8 beta-cDNA-positive clones were partially sequenced to characterize the 12 exons of the gene with sizes from 69 to 347 bp. All intron-exon junctions followed the GT-AG rule. …

GeneticsBase SequenceMolecular Sequence DataRestriction MappingNucleic acid sequenceIntronDNAExonsBiologyComplement C8Polymerase Chain ReactionMolecular biologyIntronsRestriction fragmentgenomic DNAExonRestriction mapComplementary DNAGeneticsbiology.proteinHumansCloning MolecularGenePhylogenyGenetics (clinical)Human Genetics
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Molecular diversity at the self-incompatibility locus is a salient feature in natural populations of wild tomato (Lycopersicon peruvianum)

1993

A cDNA encoding a stylar protein was cloned from flowers of self-incompatible wild tomato (Lycopersicon peruvianum). The corresponding gene was mapped to the S locus, which is responsible for self-incompatibility. The nucleotide sequence was determined for this allele, and compared to other S-related sequences in the Solanaceae. The S allele was used to probe DNA from 92 plants comprising 10 natural populations of Lycopersicon peruvianum. Hybridization was conducted under moderate and permissive stringencies in order to detect homologous sequences. Few alleles were detected, even under permissive conditions, underscoring the great sequence diversity at this locus. Those alleles that were de…

GeneticsBase SequencebiologyMolecular Sequence DataNucleic acid sequenceChromosome MappingGenetic Variationfood and beveragesLocus (genetics)Sequence alignmentPlantsGenes Plantbiology.organism_classificationLycopersiconBlotting SouthernComplementary DNAGeneticsWild tomatoAmino Acid SequenceCloning MolecularAlleleDNA ProbesMolecular BiologyGeneAllelesMolecular and General Genetics MGG
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Genetic polymorphism of human complement factor I (C3b inactivator) in the Chinese Han population.

1999

The human complement factor I (IF) polymorphism has been analysed by polyacrylamide gel isoelectric focusing electrophoresis of neuraminidase-treated EDTA plasma samples followed by immunoblotting and enzymatic detection. In a population study among 121 random individuals from Chengdu, PR China, three different common phenotypes were observed. The results show that IF is polymorphic in the Chinese population. The allele frequencies were as follows: FI*A = 0.153, FI*B = 0.847. The distribution of observed phenotypes was in accordance with the Hardy-Weinberg equilibrium. In comparison to other Asian population studies, the frequency of the IF*A allele was the highest in the Chinese population…

GeneticsChinaPolymorphism GeneticGenotypeIsoelectric focusingImmunologyComplement factor IBiologyMolecular biologyEdta plasmaChinese han populationAsian PeopleComplement Factor IC3b inactivatorGeneticsHumansPolyacrylamide gel electrophoresisGenetics (clinical)AllelesExperimental and clinical immunogenetics
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The mouseClq genes are clustered on chromosome 4 and show conservation of gene organization

1996

Mouse complement component C1q is a serum glycoprotein which consists of six A chains, six B chains and six C chains. The three polypeptides are 223, 228, and 217 residues long, respectively, and are encoded by three genes. DNA probes for mouse C1q A, B, and C chains were hybridized to Southern blots of DNA obtained from various inbred mouse strains. On the basis of fragment length polymorphisms, two different alleles of each of the genes could be identified. The distribution of these alleles was determined in the BXD and LXPL recombinant inbred strain series. Comparison with previously reported strain distribution patterns shows that the genes encoding mouseClq map to the same locus on dis…

GeneticsChromosome 4Complementary DNAImmunologyGene clusterGeneticsGenomic libraryRecombinant inbred strainLocus (genetics)BiologyGeneMolecular biologySouthern blotImmunogenetics
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Lack of linkage between gene(s) controlling the synthesis of the seventh component of complement and the HLA region on chromosome No. 6 in man.

1976

The family of an individual was studied who lacks the seventh component of complement in his serum (C7 homozygous deficiency). Both parents are C7 heterozygousdeficient. In this investigation, the following parameters were determined: complement components in functional and immunochemical tests; HLA-A,B antigens, HLA-D (MLC) determinants; the Bf system; glyoxalase I and B cell antigens. No evidence for linkage between the immunogenetic linkage group on chromosome 6 and gene(s) controlling the synthesis of the seventh component of complement was obtained. This is in accordance with the assumption that only genes controlling components of the initiating rather than the membrane attack unit of…

GeneticsChromosomes Human 6-12 and XMaleGenetic LinkageChromosomeHuman leukocyte antigenComplement System ProteinsBiologyComplement factor BHuman geneticsComplement C7Complement (complexity)medicine.anatomical_structureAntigenHLA AntigensHistocompatibility AntigensGeneticsmedicineHumansLymphocyte Culture Test MixedChildGeneGenetics (clinical)B cellHuman genetics
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Human complement C81 (C8 A) polymorphism: detection and segregation of new variants

1993

In addition to the earlier detected C81(A) rare variants A1, A2 (now A3) and B1 (now B2), six new rare variants (C81 A2 new, A4, A5, A6, M1 and B1new) are described within the polymorphism of the eighth component of human complement (alpha-gamma chain subunit). Except for A3, all rare C81 A variants are only detected by isoelectric focusing, and not by SDS polyacrylamide gel electrophoresis (PAGE), in the alpha-gamma subunit. In one individual out of approximately 700 individuals studied, a reversed position of the common allele (B vs A) was observed by SDS PAGE and the isofocusing technique. The segregation of A1, A3 and A4 could be followed in putative father/child combinations.

GeneticsComplement (group theory)Polymorphism GeneticIsoelectric focusingProtein subunitBiologyComplement C8Molecular biologyAllotypeHuman geneticsPolymorphism (computer science)GeneticsHumansElectrophoresis Polyacrylamide GelIsoelectric FocusingAllelePolyacrylamide gel electrophoresisAllelesGenetics (clinical)Human Genetics
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Complement component C3: molecular basis of the C3*S025 variant and evidence for molecular heterogeneity of other variants.

1995

Complement component 3 (C3) is the central molecule of the complement system. It displays a number of polymorphic variants with, as yet, unclear functional consequences. We have investigated a number of rare C3 variants by PCR-SSCP (polymerase chain reaction-single strand conformation polymorphism) analysis and could identify the molecular basis of a C3*S025 variant. The decreased electrophoretic mobility of this protein is caused by the exchange of a neutral serine residue to an arginine residue (positively charged). This exchange is unlikely to have functional consequences as it maps to the C-terminus of the alpha-chain. C3 variants appear to have originated from various independent mutat…

GeneticsComplement component 3biologyBase SequenceGenetic heterogeneityMolecular Sequence DataComplement C3Molecular medicinePolymerase Chain Reactionlaw.inventionComplement systemSerineGenetic HeterogeneitylawGeneticsbiology.proteinHumansGeneGenetics (clinical)Polymerase chain reactionPolymerasePolymorphism Single-Stranded ConformationalHuman genetics
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