Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Somatic cell and molecular genetics 7 (1981), S. 489-505 
    ISSN: 1572-9931
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract A karyotypically normal, chromosomally female (X/X) in vitro line of mouse teratocarcinoma stem cells was established from a malignant mouse teratocarcinoma of the 129/Sv Sl C P inbred strain. The tumor of origin was experimentally induced by ectopic transplantation of a 6-day embryo. The normal number of chromosomes was observed in 92% of metaphases of the cultured cells. This high frequency of euploidy, as well as karyotypic normalcy, were maintained during numerous passages in culture without a feeder-cell layer and after freezing and thawing of the cells. The line has been designated METT-1 (Mouse Euploid Totipotent Teratocarcinoma), signifying that it is the first such in vitro line that has proved (in tests by T. Stewart and B. Mintz, manuscript in preparation) to be developmentally totipotent, i.e., capable of both somatic and germinal differentiation when injected into blastocysts, even after freezing and thawing and prolonged culture. This unique ensemble of properties renders the cell line suitable for selection of specific mutant genes and for gene-transfer experiments in culture, for the purpose of producing from the mutant cells new strains of mice with predetermined genetic changes.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 7 (1986), S. 205-221 
    ISSN: 0192-253X
    Keywords: gene dosage effects ; Drosophila sex determination ; maternal-zygotic gene interactions ; tandem duplications ; maternal effects ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The daughterless (da) gene provides an essential maternally supplied component for Drosophila sex determination and dosage compensation. In this connection, it is required as a positive regulator of a female-specific master regulatory gene, Sex-lethal (Sxl). In addition, zygotic da gene function is required for male and female viability. Thus, the phenotype da is complex; it includes both maternal and zygotic aspects, as well as both sex-specific and nonsex-specific aspects. Assessment of wild-type da function has relied on the characterization of only a single leaky mutant da allele. In order to better understand the nature of this allele and the relationships between the various aspects of its complex phenotype, tandem duplications of both the mutant and wild-type da alleles were isolated and used in a dose study of this gene's function. Three conclusions were reached: (1) by the most stringent genetic criteria, the mutant da allele is a simple hypomorph, an allele with reduced but non-zero levels of wild-type functions; (2) since increased dose of da+ had no effect on viability or progeny sex ratio, this gene seems not to be a dose-sensitive element of the X/A ratio sex determination signal; and (3) expression of the maternal da+ allele does make a contribution to the nonsex-specific developmental processes that require zygotic da+ function; however, that contribution is clearly minor. In contrast, the zygotic genotype with respect to da appears to have no effect on the expression of Sxl+ in the zygote, the sex-specific process that requires maternal da+ function.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...