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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Planta 134 (1977), S. 155-157 
    ISSN: 1432-2048
    Keywords: RNA synthesis ; [3H]uridine uptake ; 8-hydroxyquinoline ; Matthiola
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract 8-hydroxyquinoline has been previously used as an inhibitor in studies on porphyrin metabolism, where it is thought to act by chelating iron. It is shown that this compound also rapidly inhibits uridine uptake of seedlings or cotyledons of the crucifer Matthiola incana R.Br. RNA synthesis is also affected but the inhibition is not as severe as reported for fission yeast.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2048
    Keywords: Gene mapping ; Glycine ; Restriction enzymes ; Ribosomal RNA genes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The restriction endonuclease map of the 25 S and 18 S ribosomal RNA genes of a higher plant is presented. Soybean (Glycine max) rDNA was enriched by preparative buoyant density centrifugation in CsCl-actinomycin D gradients. The buoyant density of the rDNA was determined to be 1.6988 g cm−3 by analytical centrifugation in CsCl. Saturation hybridization showed that 0.1% of the total DNA contains 25 S and 18 S rRNA coding sequences. This is equivalent to 800 rRNA genes per haploid genome (DNA content: 1.29 pg) or 3200 for the tetraploid genome. Restriction endonuclease mapping was performed with Bam H I, Hind III, Eco R I, and BstI. The repeating unit of the soybean ribosomal DNA has a molecular weight of 5.9·106 or approximately 9,000 kb. The 25 S and 18 S rRNA coding sequences were localized within the restriction map of the repeating unit by specific hybridization with either [125I]25 S or [125I]18 S rRNA. It was demonstrated that there is no heterogeneity even in the spacer region of the soybean rDNA.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular evolution 30 (1990), S. 170-181 
    ISSN: 1432-1432
    Keywords: C to T transitions ; Internal transcribed spacer ; Molecular evolution ; Processing ; Ribosomal DNA ; 5.8S rRNA gene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The internal transcribed spacer (ITS) 1 and 2, the 5.8S rRNA gene, and adjacent 18S rRNA and 25S rRNA coding regions of two Cucurbitaceae (Cucurbita pepo, zucchini, ITS 1: 187 bp, and ITS 2: 252 bp in length, andCucumis sativus, cucumber, ITS 1: 229 bp, and ITS 2: 245 bp in length) have been sequenced. The evolutionary pattern shown by the ITSs of these plants is different from that found in vertebrates. Deletions, insertions, and base substitutions have occurred in both spacers; however, it is obvious that some selection pressure is responsible for the preservation of stem-loop structures. The dissimilarity of the 5′ region of ITS 2 found in higher plants has consequences for proposed models on U3 snRNA-ITS 2 interaction in higher eukaryotes. The two investigated Cucurbitaceae species show a G+C content of ITS 1 that nearly equals that of ITS 2. An analysis of the ITS sequences reveals that in 19 out of 20 organisms published, the G+C content of ITS 1 nearly equals that of ITS 2, although it ranges from 20% to 90% in different organisms (GC balance). Moreover, the balanced G+C content of the ITSs in a given species seems to be similar to that of so-called expansion segments (ESs) in the 25/28S rRNA coding region. Thus, ITSs show a phenomenon called molecular coevolution with respect to each other and to the ESs. In the ITSs of Cucurbitaceae the balanced G+C composition is at least partly achieved by C to T transitions, via deamination of 5-methylcytosine. Other mutational events must be taken into account. The appearance of this phenomenon is discussed in terms of functional constraints linked to the structures of these spacers.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular evolution 36 (1993), S. 144-152 
    ISSN: 1432-1432
    Keywords: “Ancestor” IGS ; Cucumis ; Cucurbita ; C to T transition ; Intergenic spacer ; DNA methylation ; Ribosomal DNA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The intergenic spacer (IGS) of a 10-kbp repeat (clone pRZ7D) of the nuclear 18S, 5.8S, and 25S ribosomal RNA genes ofCucurbita pepo (zucchini) was sequenced and compared to the IGS sequences of two other Cucurbitaceae.Cucurbita maxima (squash), andCucumis sativus (cucumber). The nucleotide sequence and the structural organization of the IGS ofC. pepo andC. maxima are rather similar (between 75 and 100% sequence similarity depending on the region compared). The IGS are mainly composed of three different repeated elements interspersed into unique sequences: GC-rich clusters, a 422-bp AT-rich element including the transcription initiation site (TIS) for RNA polymerase I, and 260-bp repeats in the 5′ external transcribed spacer (D repeats). The TIS is duplicated in the 10-kbp repeat class ofC. pepo, as it is also described for the 11.5-kbp rDNA repeat ofC. maxima. The IGS ofCucumis sativus is also composed of different repeated elements; however, obvious sequence identity to theCucurbita species only occurs around the TIS and the preceding AT-rich region. GC-rich clusters with different primary sequences are present in the IGS of all three plants. Remarkably, the repeated elements in the 5′ETS accumulate TpG and TpNpG motifs, whereas CpG and CpNpG motifs less frequently occur. This accumulation might be caused by the transition of methylated cytosines (inmCpG ormCpNpG motifs) into thymidine via deamination in a previously GC-rich ancestor. The following singular region exhibits 50% G + C inC. pepo, 53% G + C inC. maxima, and 63% G + C inC. sativus. A model for a common ancestor of the 3′IGS for these Cucurbitaceae is proposed.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular evolution 41 (1995), S. 996-1005 
    ISSN: 1432-1432
    Keywords: Repetitive DNA ; Tandem repeats ; Sequence analysis ; Phylogenetic tree ; Silent repeats ; Evolution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Two different satellite DNAs exist in the genus Cucurbita which are different with respect to repeat length (350 by and 170 bp), array size, and sequence homogenization. Whereas the 350-bp satellite DNA is prominent and very homogeneous in all species investigated except for C. maxima and C. lundelliana, the 170-bp satellite is rather evenly distributed in all species. In C. maxima and C. lundelliana the 350-bp satellite is present only in small amounts, but detectable by the sensitive PCR method. These repeats are also very homogeneous, reflecting a silent stage of satellite DNA. In contrast, the 170-bp satellite DNA is intra- and interspecifically heterogeneous. It is striking that the species with no detectable amount of 350-bp satellite contain 170-bp satellite DNA clusters with the highest degree of homogeneity. The evolution of satellite DNA repeats within cultivated and wild species in the genus Cucurbita is elucidated using the sequence data of both satellite DNAs from all species investigated. The value of satellite DNA for phylogenetic analysis between closely related species is discussed.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] Here we show that the cis-acting genetic element aps (amplification-promoting sequence), isolated from the nontranscribed spacer region of tobacco ribosomal DNA (rDNA), increases the level of expression of recombinant proteins. Transgenic tobacco plants, transformed with expression cassettes ...
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 65 (1978), S. 353-358 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract DNA samples from various higher plants (Phaseolus aureus, Glycine max, Matthiola incana, Brassica pekinensis, Cucumis melo) were centrifuged in actinomycin-caesium chloride gradients and the genes coding for the ribosomal RNAs were detected by hybridisation with tritium labelled 5S and 25S+18S rRNA, respectively. With DNA of low molecular weight (〈 5×106 daltons) the 5S and 25S+18S rRNA genes are often fractionated together. A good separation of the genes for 25S+18S rRNA from the 5S rRNA genes occurred only with high molecular weight DNA (〉 10×106 daltons) indicating that at least most of the 5S rRNA genes are not linked to, or interspersed with, the genes coding for 25S and 18S rRNA. This result is in agreement with the situation in animal cells and in contrast to that reported for bacteria, lower eukaryotes and chloroplasts.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1573-5028
    Keywords: DNA-protein binding ; intergenic spacer ; repeated elements ; ribosomal DNA ; RNA polymerase I ; single-stranded DNA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Directly repeated elements have been characterized downstream of the transcription initiation site (TIS) in the 5′ external transcribed spacer (5′ ETS) of the rRNA genes of cucumber (Cucumis sativus). In order to show that these repeated elements are also involved in transcriptional regulation processes of RNA polymerase I while being single-stranded during transcription, DNA-protein binding assays were performed with synthetic oligonucleotides prepared from the promoter region as well as from the repeated elements. The single-stranded DNA of the upstream binding element (from −164 to −105), the core promoter (from −41 to +16) and a loop-forming sequence (LRE) of the repeated elements interact with the same nuclear proteins whereas another region of the repeated elements (XRE) cooperates with a different nuclear protein. Remarkably, both complementary strands show identical protein binding.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1573-5028
    Keywords: chalcone synthase ; Matthiola incana ; flavonoids ; mutants ; regulation ; flower development
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The expression of the key enzyme of flavonoid biosynthesis, chalcone synthase (CHS), has been followed in different genotypes of Matthiola incana R.Br. (Brassicaceae) which are genetically defined with respect to anthocyanin production. Enzyme activity was determined by a radioactive assay in crude flower extracts. The amount of enzyme protein in the developing flower was determined by use of SDS-PAGE, protein blotting, reaction with an antiserum against CHS of parsley (Petroselinum hortense), and PAP staining. The molecular weight of about 41 500 of the CHS subunits corresponds with that obtained from other higher plants. Steps of flower development were subdivided into stages-1,0, I–IV. During flower development of a Matthiola line with coloured petals (line 07) a defined pattern of CHS enzyme production can be observed: At the stage of bud opening (stage 0–I) a dramatic increase of the amount of CHS enzyme prodein in the petals occurs. This is quite different from results obtained with petals of the white flowering mutant line 18 bearing a genetic defect in the gene f coding for CHS. Here a reduced and nearly constant level of CHS enzyme protein can be observed during flower development. This line is most attractive for our studies of the regulation of enzyme synthesis because under stress conditions a slight colouring of the flower petals occurs, which is uniformly distributed and line-specific. This suggests that we are dealing with a CHS mutant producing a rather inactive enzyme protein at a low level. This protein may regain enzyme activity under certain environmental conditions. Preliminary investigations suggest a rather high level of CHS mRNA transcription at the bud opening stage of the flowers. Other white flowering mutant lines, line 17 (genotype ee) and line 19 (gg) with a late block in the flavonoid biosynthesis pathway, exhibit a concomitant reduction of CHS enzyme activity and protein content in comparison to anthocyanin-producing lines with the f+f+e+e+g+g+-genotype.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1573-5060
    Keywords: Cucurbitaceae ; domestication ; molecular evolution ; plant breeding ; repetitive DNA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract A new species-specific, tandemly arranged satellite (pMetSat) DNA was characterized by Southern hybridization, cloning and sequencing for Cucumis metuliferus, a cultivated species that originated in Africa. The 346 bp repeats share short stretches of remarkable sequence similarity with satellite DNA of other cultivated Cucumis species, in particular types I-IV of C. sativus (cucumber) and the 352 bp satellite of C. melo (melon), although no cross-hybridization occurs applying stringent conditions. Minor arrays of the respective repeat types were also detected in other less cultivated or wild Cucumis species by PCR amplification or long exposure of Southern blots. For the Cucumis species, the pattern of satellite distribution appears to reflect the taxonomic classification. This suggests that in ancestral species a set of differential but related repeats was already present. During speciation and cultivation, specific members of this set underwent amplifications and modifications. Differential distribution of small arrays of the Cucumis satellites within the genomes of other Cucurbitaceae (tribus Benincaseae, Trichosantheae, Sicyeae) is shown.
    Type of Medium: Electronic Resource
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