PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “Base Composition”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 289 records · Page 16Linked to original sources

Base composition and gene distribution: critical patterns in mammalian genome organization.

Recent success in developing transcriptional maps of large genomic regions provide excellent opportunities for the investigation of mammalian genome organization. Detailed definition of organizational features will, in the short term, aid in prioritizing genomic sequencing efforts and in interpreting sequencing results and, in the long term, will surely provide insights into the structural, functional and evolutionary basis for the mammalian chromosome and chromosomal banding patterns. For such efforts, human chromosome 21 provides an excellent model system because the physical and clone maps are detailed, and several transcriptional mapping projects have provided large numbers of novel genes. It is, therefore, valuable at this point to examine these transcriptional mapping data and to compare them with the isochore model of the mammalian genome, which describes patterns in base composition and predicts gene distributions. Not only do compelling organizational patterns appear, but new questions about additional possible patterns in gene size, structure, conservation and transcription can be asked.

Animals↗

Base compositions of genes encoding alpha-actin and lactate dehydrogenase-A from differently adapted vertebrates show no temperature-adaptive variation in G + C content.

There is a long-standing debate in molecular evolution concerning the putative importance of GC content in adapting the thermal stabilities of DNA and RNA. Most studies of this relationship have examined broad-scale compositional patterns, for example, total GC percentages in genomes and occurrence of GC-rich isochores. Few studies have systematically examined the GC contents of individual orthologous genes from differently thermally adapted species. When this has been done, the emphasis has been on comparing large numbers of genes in only a few species. We have approached the GC-adaptation temperature hypothesis in a different manner by examining patterns of base composition of genes encoding lactate dehydrogenase-A (ldh-a) and alpha-actin (alpha-actin) from 51 species of vertebrates whose adaptation temperatures ranged from -1.86 degrees C (Antarctic fishes) to approximately 45 degrees C (desert reptile). No significant positive correlation was found between any index of GC content (GC content of the entire sequence, GC content of the third codon position [GC(3)], and GC content at fourfold degenerate sites [GC(4)]) and any index of adaptation temperature (maximal, mean, or minimal body temperature). For alpha-actin, slopes of regression lines for all comparisons did not differ significantly from zero. For ldh-a, negative correlations between adaptation temperature and total GC content, GC(3), and GC(4) were observed but were shown to be due entirely to phylogenetic influences (as revealed by independent contrast analyses). This comparison of GC content across a wide range of ectothermic ("cold-blooded") and endothermic ("warm-blooded") vertebrates revealed that frogs of the genus Xenopus, which have commonly been used as a representative cold-blooded species, in fact are outliers among ectotherms for the alpha-actin analyses, raising concern about the appropriateness of choosing these amphibians as representative of ectothermic vertebrates in general. Our study indicates that, whereas GC contents of isochores may show variation among different classes of vertebrates, there is no consistent relationship between adaptation temperature and the percentage of thermal stability-enhancing G + C base pairs in protein-coding genes.

Actins↗

Identification of Fusobacterium species by the electrophoretic migration of glutamate dehydrogenase and 2-oxoglutarate reductase in relation to their DNA base composition and peptidoglycan dibasic amino acids.

Rapid identification of Fusobacterium spp. is hampered by their inability to ferment carbohydrates and the availability of relatively few useful phenotypic characters. In an attempt to identify new diagnostic markers for species, we reported recently the potential utility of glutamate dehydrogenase (GDH) electrophoretic mobilities for distinguishing eight species of Fusobacterium. We have extended these observations to include all recognised members of the genus except F. prausnitzii and F. perfoetens, and our results show that they cluster into three broad electrophoretic groups. Some species, such as F. periodonticum, F. simiae and F. necrophorum, possessed GDH with similar electrophoretic mobilities. However, within such clusters, the electrophoretic migration of 2-oxoglutarate reductase (OGR) distinguished between species. Neither GDH or OGR mobility alone clearly differentiated all species, but their combined use provided unambiguous discrimination of all species except F. varium and F. mortiferum. The DNA base compositions of all species except F. naviforme (ATCC 25832) and F. sulci, were within the range 26-34 mol% G + C, suggesting the genus may be homogeneous. However, the peptidoglycan composition divided the genus into two major groups that contained either lanthionine or diaminopimelic acid; F. mortiferum peptidoglycan contained both dibasic amino acids.

Alcohol Oxidoreductases↗

Organization and base composition of tilapia Hox genes: implications for the evolution of Hox clusters in fish.

Hox genes encode DNA binding proteins that specify cell fate in the anterior-posterior axis of metazoan animal embryos. While each Hox cluster contains the same genes among the different mammalian species, this does not happen in ray-finned fish, in which both the number and organization of Hox genes and even Hox clusters are variables. Ray-finned fish are believed to have undergone an additional genome duplication that led to the presence of 8 Hox clusters (four twin pairs) in their ancestor. Here we describe the Tilapia (Oreochromis niloticus) Hox genes set in terms of gene content, clusters organization and base composition and compare it with those of pufferfish and zebrafish. We observed that in all these fish, when paralogous genes are conserved in both the twin clusters, the gene which has a lower GC level generally: (i) belongs to the less gene-rich (less conserved) cluster; (ii) has a reduced field of embryonic expression; or (iii) is a pseudogene. The relationship between the decrease of GC level and the loss of conservation and function of one of the paralogous genes from twin clusters is discussed.

Animals↗

Characterization of mitochondrial DNA in various Candida species: isolation, restriction endonuclease analysis, size, and base composition.

A practical and effective method for the extraction of mitochondrial DNA from Candida species was developed. Zymolyase was used to induce yeast protoplasts, and mitochondrial DNA was extracted from DNase I-treated mitochondrial preparations. Restriction endonuclease analyses of mitochondrial DNAs from 19 isolates representing seven species of Candida (C. albicans, C. kefyr, C. lusitaniae, C. maltosa, C. parapsilosis, C. shehatae, and C. tropicalis) and Lodderomyces elongisporus revealed different cleavage patterns that appeared to be specific for the species. Few common restriction fragments were evident. The genome sizes of the mitochondrial DNAs ranged from 26.4 to 51.4 kilobase pairs, and the guanine-plus-cytosine contents ranged from 20.7 to 36.8 mol%. There was no correlation between the base compositions of nuclear and mitochondrial DNAs. Eight isolates of C. parapsilosis, including the type culture, and an ascosporogenous strain of L. elongisporus, which was once proposed as the teleomorph of C. parapsilosis, had similar mitochondrial DNA molecular sizes (30.2 and 28.8 kilobase pairs); however, restriction endonuclease patterns of these organisms were distinct. These data provide additional support for discrimination of these two species. The results of our experiments demonstrate that mitochondrial DNA analyses may provide useful criteria for the differentiation of yeast species.

Base Composition↗

Regional base composition variation along yeast chromosome III: evolution of chromosome primary structure.

The recent determination of the complete sequence of chromosome III from the yeast Saccharomyces cerevisiae allows, for the first time, the investigation of the long range primary structure of a eukaryotic chromosome. We have found that, against a background G+C level of about 35%, there are two regions (one in each chromosome arm) in which G+C values rise to over 50%. This effect is seen in silent sites within genes, but not in noncoding intergenic sequences. The variation in G+C content is not related to differential selection of synonymous codons, and probably reflects mutational biases. That the intergenic regions do not exhibit the same phenomenon is particularly interesting, and suggests that they are under substantial constraint. The yeast chromosome may be a model of the structure of the human genome, since there is evidence that it is also a mosaic of long regions of different base compositions, reflected in wide variation of G+C content at silent sites among genes. Two possible causes of this regional effect, replication timing, and recombination frequency, are discussed.

Animals↗

Two levels of information in DNA: relationship of Romanes' "intrinsic" variability of the reproductive system, and Bateson's "residue" to the species-dependent component of the base composition, (C+G)%.

In 1886 Charles Darwin's research associate George Romanes published a paper entitled "Physiological Selection: An Additional Suggestion on the Origin of Species". This was criticized by his Victorian contemporaries and largely ignored by those who followed. However, the recent recognition of two levels of information in DNA suggests that Romanes had solved the major problems with Darwin's theory. It was apparent from the outset that the form of reproductive isolation likely to apply most generally to initial species divergence (hybrid sterility), would depend on differences, not in "primary" information ("genic"), but in "secondary" information ("chromosomal"). This viewpoint, further elaborated by Bateson & Saunders (1902), White (1978), and King (1993), is criticized by the genic school (Coyne & Orr, 1998) because it requires visible differences between chromosomes, and appears not to explain Haldane's rule. However, chromosomal differentiation with respect to the species-dependent component of base composition [(C+G)%; Forsdyke, 1996] appears to resolve these problems. Because it explained so much, it was easy to believe that the genic viewpoint explained everything. Romanes and Bateson thought otherwise. We are only just beginning to recognize what they were trying to tell us.

Animals↗

Microleakage of Class V resin-based composite restorations using five simplified adhesive systems.

PURPOSE: To evaluate microleakage at enamel and dentin margins of Class V resin-based composite (RBC) restorations using five simplified adhesive systems, one self-etching adhesive, three commercial one-bottle adhesives and one experimental one-bottle adhesive. MATERIALS AND METHODS: Class V cavities (3 mm x 2 mm x 2 mm) were prepared in sound human molars with occlusal margins in enamel and gingival margins in dentin/cementum. Etch & Prime 3.0 (Degussa), Single Bond (3M), PQ1 (Ultradent), Prime & Bond NT (Dentsply) and Experimental BEH (Dentsply DeTrey) were applied strictly according to manufacturers instructions. All adhesive systems were applied on etched substrates, except for the self-etching adhesive Etch & Prime 3.0. Cavities were restored with Z100 RBC. After finishing and polishing, teeth were thermo-cycled (x 700, 5-55 degrees C, 60 s dwell time). Specimens were coated with nail varnish, immersed in silver nitrate for 2 hours and sectioned longitudinally with a diamond disc. The extent of leakage was measured and ranked using a 0-4 scale. RESULTS: Statistical analysis using Kruskal-Wallis test revealed significantly higher leakage scores (P < 0.001) for Etch & Prime 3.0 on enamel when compared to all other adhesive systems. Regarding dentin margins none of the systems completely eliminated microleakage. PQ1 had significantly lower scores (P < 0.05) when compared to Etch & Prime 3.0 and Single Bond. No statistically significant difference was observed for the other groups.

Bisphenol A-Glycidyl Methacrylate↗

Effect of plasma arc curing on the microleakage of Class V resin-based composite restorations.

PURPOSE: To evaluate the effect of plasma arc light-curing on the microleakage of Class V resin-based composite (RBC). MATERIALS AND METHODS: Facial and lingual Class V cavities were prepared at the cemento-enamel junction of extracted third molars. Restorations of the two materials (Z250; Amelogen) were placed, using the supplied dentin adhesives (Single Bond; PQ 1, respectively), and light-cured by either a halogen light curing unit (H) or a plasma arc curing unit (P). After thermal cycling, the teeth were immersed in methylene blue dye, then sections of the restored teeth were visually assessed for leakage. RESULTS: No leakage was observed at the interface between enamel and RBC in any restoration in this study. At gingival margins, the incidence of leakage (slight/severe) was: Z250 H = 2/4, P = 6/6; Amelogen H = 3/4, P = 1/12, where n = 16. The greatest incidence of leakage was observed in restorations cured by the plasma arc method. A two-way ANOVA of leakage data rankings showed curing method to be a significant factor (P = 0.002), restorative material not to be a significant factor (P = 0.24), and no significant interaction between material and curing method (P = 0.38).

Analysis of Variance↗

Influence of Erbium:YAG laser energies on the microleakage of Class V resin-based composite restorations.

PURPOSE: To evaluate the influence of three Erbium:YAG laser energies on the microleakage of Class V resin-based composite restorations. MATERIALS AND METHODS: 60 extracted human premolar teeth stored in 0.12% thymol solution were randomly allocated to three groups. Buccal and lingual box-shaped Class V cavities were prepared on each tooth. One cavity served as the control and was cut using a conventional diamond bur in a high-speed handpiece. The test cavity was prepared using a pulse repetition rate of 5 Hz with 1 of 3 pulse energies; 200 mJ, 240 mJ, and 300 mJ with a 100 mJ dentin finish. The cavities were restored with Scotchbond Multi-Purpose and Z100 and were finished immediately before being stored for 3 months in thymol solution at 37 degrees C. Following thermocycling between 5 degrees C and 55 degrees C for 240 cycles and a further 12 hrs storage, the teeth were immersed in a 2% aqueous solution of methylene blue for 24 hrs. They were then sectioned through the mid-point of the restorations in a bucco-lingual plane and dye penetration was scored as 0 (none) to 4 (to the axial wall) for the enamel and dentin margins of both sections. The worst score for each margin was used for statistical analysis using the Kruskal Wallis and Mann-Whitney U tests at P < 0.05. RESULTS: When the lased groups were compared, optimum sealing was achieved with energies of at least 240 mJ at the enamel margin and with energies no higher than 200 mJ to finish the dentin margin. However, while all the pulse energies compared favorably to the control group in enamel, a similar result was found only using the 300 mJ, with 100 mJ, finish at the dentin margins.

Aluminum Silicates↗

Stress reduction in resin-based composites cured with a two-step light-curing unit.

PURPOSE: To examine the stress reduction of different resin-based composites, cured with a two-step polymerization unit (Elipar Highlight) by means of a photoelastic investigation. MATERIALS AND METHODS: For each material (Pertac II, Tetric Ceram, Charisma F, Solitaire, Dyract, Dyract AP, Definite), a minimum of 10 resin samples, embedded in acrylic-glass plates, were polymerized using a standard polymerization process of 700 mW/cm for 40 s. Another 10 samples were polymerized with a light output of 150 mW/cm2 for 10 s and then with a light output of 700 mW/cm2 for 30 s. RESULTS: For Pertac II the reduction of polymerization stress in the two-step-mode was 15.5%, for Tetric Ceram 14.5%, for Solitaire 8.1%, for Dyract AP 6.5% and for Definite 4.7%. These differences in polymerization stress between the standard and two-step-polymerization mode were statistically significant (P < 0.01, Wilcoxon test). No statistically significant differences in polymerization stress could be found for Charisma F and Dyract.

Bisphenol A-Glycidyl Methacrylate↗

Wettability of some packable resin-based composites. An in vitro study.

The purpose of this research was to measure the contact angles of some packable resin-based composites in order to determine their wettability related to the surface energy. Materials were manipulated according to the manufacturer's instructions and were inserted in a circular metallic matrix and photo cured for 40 seconds on both sides. The specimens were removed and finished with silicon carbide metallurgical finishing paper (800 gifts). Half of each specimen was covered by a layer of Bis-GMA and photo cured for 20 seconds. The specimens were then submitted to measurements in a contact angle goniometer with two different liquids and polarities in three points. The materials without Bis-GMA covering layer showed statistically significant differences related to contact angles and among the materials and liquids (p<0/05).

Bisphenol A-Glycidyl Methacrylate↗

A test of translational selection at 'silent' sites in the human genome: base composition comparisons in alternatively spliced genes.

Natural selection appears to discriminate among synonymous codons to enhance translational efficiency in a wide range of prokaryotes and eukaryotes. Codon bias is strongly related to gene expression levels in these species. In addition, between-gene variation in silent DNA divergence is inversely correlated with codon bias. However, in mammals, between-gene comparisons are complicated by distinctive nucleotide-content bias (isochores) throughout the genome. In this study, we attempted to identify translational selection by analyzing the DNA sequences of alternatively spliced genes in humans and in Drosophila melanogaster. Among codons in an alternatively spliced gene, those in constitutively expressed exons are translated more often than those in alternatively spliced exons. Thus, translational selection should act more strongly to bias codon usage and reduce silent divergence in constitutive than in alternative exons. By controlling for regional forces affecting base-composition evolution, this within-gene comparison makes it possible to detect codon selection at synonymous sites in mammals. We found that GC-ending codons are more abundant in constitutive than alternatively spliced exons in both Drosophila and humans. Contrary to our expectation, however, silent DNA divergence between mammalian species is higher in constitutive than in alternative exons.

Alternative Splicing↗

The relationship between the base composition of bacterial DNA and its intracellular melting temperature as determined by differential scanning calorimetry.

The correlation between the melting temperature of intracellular DNA, determined by differential scanning calorimetry (DSC) of whole bacteria, and its guanine + cytosine (G + C) content, was examined for 58 species of bacteria. Samples of vegetative cells were heated in a Perkin-Elmer DSC-2C at 10 degrees C min-1 from 5 to 130 degrees C, cooled to 5 degrees C and then re-heated as before. Literature values for the mole fraction of G + C, XGC, were linearly related to the temperature, Tmax, at which the reversible peak, pr, observed on the second heating run was at a maximum, via the equation XGC = (Tmax -73.8)/41.0. This equation accounted for 91.9% of the variance in XGC with 95% confidence limits of +/- 7.3%, approximately 1.6 times the corresponding uncertainty (+/- 4.5%) quoted by De Ley (Journal of Bacteriology 101, 738-754, 1970) for estimates based on the spectroscopically determined melting temperature of purified DNA. Random errors of measurement of Tmax did not greatly limit the precision of the prediction and it was concluded that factors additional to base composition affected the temperature of DNA melting within the bacterial cell. Displacement of Tmax values from the fitted line was particularly noticeable in Campylobacter, Corynebacterium and Bacterionema species and part of the residual variation appeared to be species specific, possibly caused by differences in intracellular solute concentration.

Base Composition↗

Phylogenetic diversity, polyamine pattern and DNA base composition of members of the order Planctomycetales.

The 16S rDNA sequences of 20 novel isolates of members of the order Planctomycetales were compared to those of the type strains of described planctomycete species and 22 planctomycete isolates for which the 16S rDNA sequences had been previously determined. The novel isolates could be assigned to several phylogenetically broad groups, four of which are defined by the genera Gemmata, Isosphaera, Planctomyces and Pirellula. To evaluate polyamines as a chemotaxonomic marker within this order, the polyamine pool was determined for six planctomycete reference species and for 20 planctomycete isolates. All analysed members of the order Planctomycetales contained significant amounts of polyamines. sym-Homospermidine (HSPD) is present in all strains except Planctomyces limnophilus and related strains, which had high amounts of putrescine (PUT) as the dominant polyamine component. The distribution of PUT, HSPD and spermidine reflects the phylogenetic diversity within the Planctomycetales as closely related representatives of the phylogenetic groups defined by described species and novel isolates exhibit similar polyamine patterns. Determination of the DNA base composition revealed G + C contents of > 60 mol% for members of Gemmata and Isosphaera whereas, except for two isolates, strains which are phylogenetically associated with Planctomyces and Pirellula had G + C contents of 51-57 mol%.

Bacteria↗

Template switches during plus-strand DNA synthesis of duck hepatitis B virus are influenced by the base composition of the minus-strand terminal redundancy.

Two template switches are necessary during plus-strand DNA synthesis of the relaxed circular (RC) form of the hepadnavirus genome. The 3' end of the minus-strand DNA makes important contributions to both of these template switches. It acts as the donor site for the first template switch, called primer translocation, and subsequently acts as the acceptor site for the second template switch, termed circularization. Circularization involves transfer of the nascent 3' end of the plus strand from the 5' end of the minus-strand DNA to the 3' end, where further elongation can lead to production of RC DNA. In duck hepatitis B virus (DHBV), a small terminal redundancy (5'r and 3'r) on the ends of the minus-strand DNA has been shown to be important, but not sufficient, for circularization. We investigated what contribution, if any, the base composition of the terminal redundancy made to the circularization process. Using a genetic approach, we found a strong positive correlation between the fraction of A and T residues within the terminal redundancy and the efficiency of the circularization process in those variants. Additionally, we found that the level of in situ priming increases, at the expense of primer translocation, as the fraction of A and T residues in the 3'r decreases. Thus, a terminal redundancy rich in A and T residues is important for both plus-strand template switches in DHBV.

Animals↗

Control of bone bleeding at the sternum and iliac crest donor sites using a collagen-based composite combined with autologous plasma: results of a randomized controlled trial.

In a randomized controlled trial, hemostatic effectiveness of a collagen-based composite (experimental group) was compared with standard hemostatic methods (ie, electrocautery and collagen sponge) (control group) at two bone sites. Hemostatic success, time to "controlled bleeding," and time to "complete hemostasis" were determined at the sternal edge following median sternotomy (n=64) and at the iliac crest following bone graft harvest (n=19). Almost twice the percentage of sternal edge patients (83% versus 44%, P=.002) and nearly three times the percentage of iliac crest patients (83% versus 29%, P<.05) achieved complete hemostasis in the experimental group compared to controls. Time to controlled bleeding and complete hemostasis for all bone sites also favored the experimental group over the control group at highly significant levels (P<.0001 for most comparisons). There were no adverse events related to experimental treatment use. The results support the use of this investigational hemostatic agent to control cancellous bone bleeding.

Adult↗

Base composition differences between avian myeloblastosis virus transfer RNA and transfer RNA isolated from host cells.

Using a novel chemical tritium derivative method, we have determined the base composition of 4S RNA isolated from an RNA tumor virus, the avian myeloblastosis virus, and from normal and neoplastic host cells. Extensive differences were detected, particularly with respect to the amount of methylated bases in the viral RNA. The viral 4S RNA, which fulfills the criteria for designation as transfer RNA, appears to be derived from a precursor pool that is different from the precursor population of host-cell 4S RNA. These results are discussed in regard to the possible relationship between transfer RNA of avian mycoblastosis virus and cellular transfer RNA.

Animals↗