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  • 1
    Electronic Resource
    Electronic Resource
    Identification of novel genes specifically expressed in Chlamydomonas reinhardtii zygotes (1991)
    Springer
    Plant molecular biology 16 (1991), S. 937-946 
    Details
    ISSN: 1573-5028
    Keywords: Chlamydomonas ; zygote germination ; zygote maturation ; zygote specific genes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The maturation of zygotes formed by the fusion of two gametes is the essential part of the diploid phase of the Chlamydomonas reinhardtii sexual life cycle and results in mature zygotes competent to germinate. To understand the molecular mechanisms underlying zygote maturation and the attainment of competence for germination we isolated genomic clones representing three different genes that are specifically expressed in Chlamydomonas reinhardtii zygotes. Accumulation of the RNAs started more than 24 h after mating, setting these genes apart from genes expressed in young zygotes [9]. Upon light-induced germination of zygotes, the mRNAs disappeared. The patterns of RNA accumulation and disappearance were gene-specific and suggested a function of these genes in maturation and/or in initial steps of germination.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00016066
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Characterization of two class II chitinase genes from peanut and expression studies in transgenic tobacco plants (1996)
    Springer
    Plant molecular biology 30 (1996), S. 351-358 
    Details
    ISSN: 1573-5028
    Keywords: Arachis hypogaea ; Botrytis cinerea ; chitinase ; fungal elicitior ; ethylene ; salicylate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Two different genes encoding class II chitinases from peanut (Arachis hypogaea L. cv. NC4), A.h.Chi2;1 and A.h.Chi2;2, have been cloned. In peanut cell suspension cultures, mRNA levels of A.h.Chi2;2 increased after ethylene or salicylate treatment and in the presence of conidia from Botrytis cinerea. The second gene, A.h.Chi2;1, was only expressed after treatment with the fungal spores. Transgenic tobacco plants containing the complete peanut A.h.Chi2;1 gene exhibited essentially the same expression pattern in leaves as observed in peanut cell cultures. Expression characteristics of transgenic tobacco carrying a promoter-GUS fusion of A.h.Chi2;1 are described.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00020121
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    A genetic analysis of quantitative resistance to late blight in potato: towards marker-assisted selection (1999)
    Springer
    Molecular breeding 5 (1999), S. 399-415 
    Details
    ISSN: 1572-9788
    Keywords: potato ; late blight ; quantitative resistance ; marker-assisted selection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Late blight caused by the oomycete Phytophthora infestans is the most important fungal disease in potato cultivation worldwide. Resistance to late blight is controlled by a few major genes (R genes) which can be easily overcome by new races of P. infestans and/or by an unknown number of genes expressing a quantitative type of resistance which may be more durable. Quantitative resistance of foliage to late blight was evaluated in five F1 hybrid families originating from crosses among seven different diploid potato clones. Tuber resistance was evaluated in four of the families. Two of the families were scored for both foliage maturity and vigour. The five families were genotyped with DNA-based markers and tested for linkage with the traits analysed. QTL (quantitative trait locus) analysis identified at least twelve segments on ten chromosomes of potato having genes that affect reproducibly foliage resistance. Two of those segments also have major R genes for resistance to late blight. The segments are tagged by 21 markers that can be analyzed based on PCR (polymerase chain reaction) with specific oligonucleotide primers. One QTL was detected for tuber resistance and one for foliage vigour. Two QTLs were mapped for foliage maturity. Major QTL effects on foliage and tuber resistance to late blight and on foliage maturity and vigour were all linked with marker GP179 on linkage group V of potato. Plants having alleles at this QTL, which increased foliage resistance, exhibited decreased tuber resistance, later maturity and more vigour.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1009623212180
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    Paper (German National Licenses)
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  • 4
    Electronic Resource
    Electronic Resource
    Expression of a reporter gene is reduced by a ribozyme in transgenic plants (1994)
    Springer
    Molecular genetics and genomics 245 (1994), S. 465-470 
    Details
    ISSN: 1617-4623
    Keywords: Gene regulation ; Ribozyme ; npt-gene ; Transgenic tobacco ; Genetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A chimeric gene encoding a ribozyme under the control of the cauliflower mosaic virus (CaMV) 35S promoter was introduced into transgenic tobacco plants. In vivo activity of this ribozyme, which was designed to cleave npt mRNA, was previously demonstrated by transient expression assays in plant protoplasts. The ribozyme gene was transferred into transgenic tobacco plants expressing an rbcS-npt chimeric gene as an indicator. Five double transformants out of sixteen exhibited a reduction in the amount of active NPT enzyme. To measure the amount of ribozyme produced, in the absence of its target, the ribozyme and target genes were separated by genetic segregation. The steady-state concentrations of ribozyme and target RNA were shown to be similar in the resulting single transformants. Direct evidence for a correlation between reduced npt gene expression and ribozyme expression was provided by crossing a plant containing only the ribozyme gene with a transgenic plant expressing the npt gene under control of the 35S promoter, i.e. the same promoter used to direct ribozyme expression. The expression of npt was reduced in all progeny containing both transgenes. Both steady-state levels of npt mRNA and amounts of active NPT enzyme are decreased. In addition, our data indicate that, at least in stable transformants, a large excess of ribozyme over target is not a prerequisite for achieving a significant reduction in target gene expression.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00302259
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    Paper (German National Licenses)
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