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  • 1
    ISSN: 1573-5060
    Keywords: Pelargonium × hortorum ; Pelargonium ; fertilization ; embryo survival ; plastid crosses ; genetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The 6×6×4 analysis of variance of the mean percentage embryo survival for six variegated cultivars of Pelargonium × hortorum Bailey, with mutant plastids in their germ layers, and for their isogenic green (G) clones, shows highly significant differences between females (81 to 91 per cent) and between plastid crosses (83 to 91 per cent). Between cultivar differences are attributed largely to additive effects corresponding to additive gene action, and between plastid differences to a lower survival after crosses with white (W) males than with green males. The relationship between overall fertility (% fertilization × survival) and plastid crosses is a stepwise decline in the order G×G〉G×W〉W×G〉W×W (28 to 19 per cent) in which the white embryos growing in a white mother are approximately 30 per cent less fertile than the green embryos in a green mother. The non-surviving embryos are classified into empty, undeveloped and dwarf embryos and submitted to a 6×4 analysis of variance after summing through males. The significant heterogeneity between females is attributed largely to a difference between one cultivar-with a high frequency of dwarf and a low frequency of undeveloped embryos-and the other five cultivars. The absence of a significant plastid effect upon any stage of embryo breakdown indicates that the depressive effect of white plastids is spread evenly throughout development.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-5060
    Keywords: Pelargonium x hortorum ; pelargonium ; flower doubleness ; nectary spur ; genetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The formation of single flowers of 5 petals and 5 sepals is determined by the homozygous recessive state, dd, of the doubleness gene, D/d, which is epistatic to modifying genes determining flower type. In the presence of the dominant allele, i.e. genotypes DD or Dd, the flowers are semi-double or double. Owing to the D allele alone, the single frequency of 5 petals and 5 sepals is doubled to 10 petals and 10 sepals, of which up to 5 are petaloid, to give a semi-double flower. In addition, in the presence of the D allele, three modifying loci M1/m1, M2/m2, and M3/m3 are activated to give a series of distinct doubles with integral multiples of the basic perianth number. The homozygous recessive genes m1m1 and m2m2 both add an increment of 10 perianth parts, and m3m3 adds an increment of 20 perianth parts. In heterozygotes, M1m1, M2m2 and M3m3, the dominant alleles inhibit the incremental effect of their corresponding recessive alleles. The single flower cultivars investigated probably have the genotype dd, M1M1, M2M2, M3M3 and the semi-double cultivars the genotype Dd, M1m1, M2M2, M3M3. The single flowers have a nectariferous spur, characteristic of the genus, adnate to the pedicel. As the spur is absent from semi-double and double flowers, its presence is assumed to be either a pleiotropic effect of the single flower gene, or to be controlled by an unidentified gene tightly linked with it.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Euphytica 33 (1984), S. 169-176 
    ISSN: 1573-5060
    Keywords: Mirabilis jalapa ; marvel of Peru ; four o'clock ; leaf variegation ; mutable genes ; controlling elements ; genetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The recurrent back-mutation from homozygous recessive chlorina to heterozygous dominant green in leaves of variegated Mirabilis jalapa is explicable on the hypothesis of a controlling element system. The analysis of variance of mutation frequency suggests that there is polygenic control modifying the major regulatory gene, an idea which is supported by a significant parent offspring regression. There is also evidence for a change of state in the regulatory element giving rise to a new mutability pattern.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-3297
    Keywords: Quantitative trait locus ; recombinant inbred strains ; open-field activity ; mouse ; genetics ; Pomc1 ; proopiomelanocortin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Psychology
    Notes: Abstract Various lines of evidence suggest that a polymorphism in the gene for proopiomelanocortin, Pomc1, might account for some portion of the genetic variance for open-field activity in the LS × SS RI strains. To test this hypothesis, approximately 1600 bp of Pomc1was sequenced from genomic DNA of seven of the LS × SS strains. Two distinct alleles containing a total of five single-base pair differences were detected. A substitution was found in the coding region causing a Pro-to-Ser conversion, two substitutions occurred in the 3′ untranslated region of the mRNA, and a substitution and a deletion were detected in the 3′ untranscribed flanking region. The fragment containing the coding region substitution was sequenced in an additional 15 of the LS × SS strains. A total of 12 strains contained one form of the allele, while 10 had the other. The strain distribution pattern of open-field activity scores between the two alleles suggests that these alleles do not contribute to the genetic variation of open-field activity in the LS × SS RI strains.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-3297
    Keywords: Quantitative trait locus ; recombinant inbred strains ; locomotor activity ; mouse ; genetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Psychology
    Notes: Abstract The finding that stress-induced locomotor activity exhibited a significant strain × time interaction in the LS × SS RI strains prompted examination of QTL influencing this behavior as a function of time. The degree of genetic determination for locomotor activity was 0.26 for the first 5 min and decreased to 0.16 for the last 5 min of a 30-min test but the number of genetic factors stayed relatively constant (three or four) across time. A QTL point analysis revealed a total of 15 QTL, 5–8 per 5-min time block. Few of the QTL were detected across all time points and different combinations of QTL were evident for each time period. Five of the QTL were in common with those reported by other investigators for similar behaviors. The results suggest that locomotor behavior is under a greater degree of genetic control during the initial part of the test but environmental factors become increasingly important as the test progresses. Furthermore, different genetic factors appear to be mediating genetic variation in locomotor behavior at any given time point.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Behavior genetics 12 (1982), S. 111-121 
    ISSN: 1573-3297
    Keywords: neurotransmitters ; genetics ; quantitative genetics ; pharmacology ; environment ; genetic correlations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Psychology
    Notes: Abstract Genetic studies of neurotransmitter processes to date differ from most behavioral genetic studies in that the former have rarely considered individual variability, have tended to look only for single-gene effects, and generally have overlooked or ignored environmental influences. After examining these differences, we suggest that a rapprochement between the two fields will yield synergistic benefits in studies of the genetics of neuropharmacological processes as they affect behavior.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Behavior genetics 23 (1993), S. 153-162 
    ISSN: 1573-3297
    Keywords: genetics ; selective breeding ; initial sensitivity ; ethanol ; acute tolerance ; mice rats ; chronic tolerance ; SS, LS ; HAS, LAS ; ANT, AT ; FAST, SLOW ; COLD, HOT
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Psychology
    Notes: Abstract Selective breeding for initial sensitivity to ethanol has been carried out by a number of investigators in order to investigate the mechanisms by which ethanol brings about a myriad of effects on the mammalian central nervous system. In addition the availability of these selectively bred animals provides clues to the causes of the genetic predisposition of humans to alcoholism. Eventually it is envisioned that the synteny between the mouse and human genomes will allow identification of specific genes responsible for acute effects of ethanol in both species as well as clues as to how alcoholism in humans can be better identified, prevented, and treated.
    Type of Medium: Electronic Resource
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