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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 14 (1963), S. 310-329 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary In the mealy bug, Planococcus citri, following high dosage paternal irradiation (60,000–120,000 rep), the survivors are mostly female (about 30–40% of the unirradiated control value) whereas very few males survive (about 5% of control value). After lower doses of paternal irradiation (P. I.), however, few or no females survive while the normal number of males (never less than the control value) survive. The females developing after high dosage P. I. are gynogenetic and are triploid or diploid or 3N/2N or 2N/N mosaics (Chandra 1963). The cytology of X1 embryos following 90,000 rep is described in this report, in comparison with data from embryos following lower doses (8,000 r) of P. I. and unirradiated controls, to illustrate the chromosomal mechanisms leading to the production of gynogenetic females and the probable reasons for lethality of X1 males after heavy P. I. It has been shown that triploid females stem from a fusion nucleus of the first and second polar bodies. This triploid polar nucleus, which normally participates in the formation of a polyploid sector in the young embryo, undertakes a successful embryogeny in many embryos when the zygote nucleus is unable to do so because of the heavily damaged paternal complement of chromosomes. Since the chromosomes are characterized by holokinetic activity, the irradiated paternal set manages to divide with the maternal complement but did not always segregate as successfully. Restitution divisions of the zygotic nuclei result in haploid, hyperhaploid, diploid and polyploid nuclei. Most of the diploid gynogenetic females probably originate from diploid nuclei of zygotic origin although it is possible that a few diploid females and the 2N/N mosaic females develop from polar bodies.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 14 (1963), S. 330-346 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary When females of the mealy bug. Planococcus citri, are mated to males previously irradiated with heavy doses of gamma rays (30,000 to 120,000 rep), the progeny is mostly female. These X1 females are gynogenetic, with unbroken chromosomes. Detailed cytology of 17 such gynogenetic females showed triploids, diploids. 3N/2N and 2N/N mosaics. Most of the embryos produced by triploid mothers were aneuploid and these degenerated before gastrulation. Regardless of aneuploidy, male embryos showed the typical lecanoid heterochromatization of the paternal set of chromosomes. Just prior to degeneration, the euchromatic chromosomes in the aneuploid male embryos showed endomitotic splitting while the heterochromatic did not. Among the progeny of 3N ♀ X 2N ♂ matings, only males with 5 euchromatic + 5 heterochromatic chromosomes and females with 10 or 15 euchromatic chromosomes were found. A search for adults with 5 heterochromatic +10 euchromatic chromosomes among the progeny of triploid mothers was unsuccessful. Chromosomal variables such as aneuploidy of the euchromatic set, haploidy and fragmentation are discussed in relation to the problems of heterochromatization of the paternal set and sex determination in this species.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 21 (1967), S. 211-220 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Somatic chromosomes of six specimens belonging to the following five species of artiodactyls (Artiodactyla: Mammalia) are described: A female nilgai (Boselaphus tragocamelus), 2n=46; male baresingha (Rucervus duvauceli), two specimens, 2n=56; a female Himalayan tahr (Hemitragus jemlahicus), 2n=48; a female Kirk's dik-dik (Rhynchotragus kirki), 2n=46; and a male sambar (Cervus unicolor), 2n=58. In the baresingha and the sambar, one or more acrocentric chromosomes carried satellites on their long arms. 3H-thymidine radioautographs of cultured cells of the Himalayan tahr showed a long acrocentric chromosome to be late-replicating, suggesting that it is an X chromosome.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract In mealybugs, chromatin condensation is related to both genomic imprinting and sex determination. The paternal chromosomal complement is condensed and genetically inactive in sons but not in daughters. During a study of chromatin organization in Planococcus lilacinus, digestion with micrococcal nuclease showed that 3% to 5% of the male genome is resistant to the enzyme. This Nuclease Resistant Chromatin (NRC) apparently has a nucleosomal organization. Southern hybridization of genomic DNA suggests that NRC sequences are present in both sexes and occur throughout the genome. Cloned NRC DNA is A+T-rich with stretches of adenines similar to those present in mouse α-satellite sequences. NRC DNA also contains sequence motifs that are typically associated with the nuclear matrix. Salt-fractionation experiments showed that NRC sequences are matrix associated. These observations are discussed in relation to the unusual cytological features of mealybug chromosomes, including the possible existence of multiple centres of inactivation.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 253 (1975), S. 165-168 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Chromosome imprinting is the process by which one of two genetically homologous chromosomes is predetermined to function differently from the other at a subsequent stage in development. In the coccid insects, imprinting occurs in the egg, at the time of fertilisation; it probably occurs at the same ...
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 319 (1986), S. 18-18 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] SIR-D.A. Smith (Nature 315, 103; 1985) uses the term "dosage compensation" to mean that effect on the rate of transcription of X-linked genes in the male which enables it to survive the lack of one X chromosome; X inactivation in the female is, then, a further compensatory step to enable it to get ...
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. In mealybugs, chromatin condensation is related to both genomic imprinting and sex determination. The paternal chromosomal complement is condensed and genetically inactive in sons but not in daughters. During a study of chromatin organization in Planococcus lilacinus, digestion with micrococcal nuclease showed that 3% to 5% of the male genome is resistant to the enzyme. This Nuclease Resistant Chromatin (NRC) apparently has a nucleosomal organization. Southern hybridization of genomic DNA suggests that NRC sequences are present in both sexes and occur throughout the genome. Cloned NRC DNA is A+T-rich with stretches of adenines similar to those present in mouse α-satellite sequences. NRC DNA also contains sequence motifs that are typically associated with the nuclear matrix. Salt-fractionation experiments showed that NRC sequences are matrix associated. These observations are discussed in relation to the unusual cytological features of mealybug chromosomes, including the possible existence of multiple centres of inactivation.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 193 (1984), S. 384-388 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A model is suggested for mammalian male determination based on interactions postulated to occur among an autosomal repressor gene, an X-linked male-determining gene termed Tdx, and multiple copies of certain DNA sequences on the Y chromosome that do not code for any protein. The repressor, synthesised in limited amounts, has higher affinity for the Y-linked sequences than for Tdx and its affinity for Tdx is greater than that of RNA polymerase. In XY cells the Y effectively binds all available repressor, permitting transcription of Tdx to occur. In XX cells, since competition from the Y-linked high-affinity sequences is absent, the repressor binds to Tdx and prevents transcription. As a result of this competition between Tdx and the Y-linked high-affinity sites for limiting concentrations of the autosomal repressor, the product of the Tdx gene (TDX) is synthesized in the male but not in the female. It is suggested that in determination of the male sex, the role of the Y chromosome is to serve as a sink for the Tdx repressor. The proposed interactions provide a plausible explanation for the genetic properties of several anomalies of sexual development in mouse, man, and other mammals. The model suggests that the postulated multiple, highaffinity sequences on the Y chromosome of the mouse are included among the DNA sequences referred to as the Sxr-Bkm sequences.
    Type of Medium: Electronic Resource
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