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  • Key words Yeast  (1)
  • Stereology  (1)
  • Springer  (2)
  • Institute of Physics
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  • Springer  (2)
  • Institute of Physics
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  • 1
    ISSN: 1432-0983
    Keywords: Key words Yeast ; RPD3 (REC3) ; Mitotic recombination
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Prior research identified the recessive rec3-1ts mutation in Saccharomyces cerevisiae which, in homozygous diploid cells, confers a conditional phenotype resulting in reduced levels of spontaneous mitotic recombination and loss of sporulation at the restrictive temperature of 36 °C. We found that a 3.4-kb genomic fragment that complements the rec3-1ts/rec3-1ts mutation and which maps to chromosome XIV, is identical to RPD3, a gene encoding a histone de-acetylase. Sporulation is reduced in homozygous diploid strains containing the rec3-1ts allele at 24 °C, suggesting that this allele of RPD3 encodes a gene product with a reduced function. Sporulation is abolished in diploid strains homozygous for the rpd3Δ or rec3-1ts alleles, as well as in rpd3Δ/rec3-1ts heteroallelic diploids, at the non-permissive temperature. Acid-phosphatase expression has been shown to be RPD3 dependent. We found that acid-phosphatase activity is greater in diploid strains homozygous for the temperature-sensitive rec3-1ts allele than in RPD3/RPD3 strains and increased further when mutant strains are grown at 36 °C. We also tested the rpd3Δ/rpd3Δ strains for their effects on spontaneous mitotic recombination. By assaying a variety of intra- and inter-genic recombination events distributed over three chromosomes, we found that in the majority of cases spontaneous mitotic recombination was reduced in diploid rpd3Δ/rpd3Δ cells (relative to a RPD3/RPD3 control). Finally, although 90% of mitotic recombinant events are initiated in the G1 phase of the growth cycle (i.e., before DNA synthesis) we show that RPD3 is not regulated in a cell-cycle-dependent manner. These data suggest that mitotic recombination, in addition to gene expression, is affected by changes in chromatin architecture mediated by RPD3.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 200 (1979), S. 193-203 
    ISSN: 1432-0878
    Keywords: Mosquitoes ; Midgut ; Ultrastructure ; Stereology ; Function
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Description / Table of Contents: Zusammenfassung Morphometrische Untersuchungen des Magenepithels von A. aegypti weisen darauf hin, daß die Verdauung des ersten Blutmahls in eine Reihe von Phasen gegliedert werden kann, die sich mit physiologischen Daten aus der Literatur korrelieren lassen. In einer Phase Ia (0–10 h nach Blutmahl [BM]) entfalten sich die “whorls” des rauhen endoplasmatischen Retikulums, die Golgi-Zonen werden größer, und das basale Labyrinth wird erweitert. Dies stimmt mit Synthese- und Sekretionsprozessen (z.B. peritrophische Membran, Esterasen, Lipasen) und mit Transportvorgängen durch das Magenepithel überein. In Phase Ib (10–20 h nach BM) nehmen die gemessenen zellulären Parameter weiter zu und weisen damit auf hohe Synthese- und Sekretionsaktivitäten (z.B. Verdauungsenzyme) hin. In Phase Ic (20–30 h nach BM) zeigen die an Synthese und Sekretion beteiligten Zellstrukturen, in Übereinstimmung mit der maximalen Proteasenaktivität im Darm, immer noch hohe Werte. Vergrößerte Mikrovillioberfläche, auffallende Lipideinschlüsse und Auftreten von Glykogendepots im Magenepithel deuten auf erhöhte Resorptions-, Speicher- und Transportfunktionen der Zellen hin. In Phase II (30–36 h nach BM) läßt sich anhand der strukturellen Veränderungen der Wechsel von Synthese- und Sekretionvorgängen zu Resorption, teilweiser Speicherung und Transport von Verdauungsprodukten erkennen. In Phase III (36–72 h nach BM) wird der Zellapparat in Übereinstimmung mit dem Ende der Verdauung reduziert. Lipid- und Glykogendepots werden mobilisiert und verschwinden fast vollständig aus den Magenepithelzellen.
    Notes: Summary Morphometric analysis of the epithelial lining of the stomach of A. aegypti suggests that digestion of the first blood meal in the stomach of this species can be viewed as a series of phases that can be correlated with physiological data from the literature. In phase Ia (0–10 h after blood meal [abm]) the whorls of the rough endoplasmic reticulum unfold, the Golgi zones increase, and the basal labyrinth is enlarged. This coincides with processes of synthesis and secretion (e.g., peritrophic membrane, esterases and lipases) and transport by the stomach epithelium. In phase Ib (10–20 habm) the cellular parameters measured further increase, indicating high synthetic and secretory activities (e.g., digestive enzymes). In phase Ic (20–30 habm) cell structures involved in synthesis and secretion still exhibit high values coinciding with maximal activity of proteases in the gut. Enhanced surface area of microvilli, prominent lipid inclusions, and appearance of glycogen deposits in the gut epithelium suggest increased absorption, storage, and transport functions of the stomach cells. In phase II (30–36 habm) structural alteration points to a gradual shift from synthesis and secretion to absorption, partial storage, and transport of nutrients. In phase III (36–72 habm) the cellular apparatus is reduced concomitant with the ending of the digestive cycle. Lipid inclusions and glycogen deposits disappear from the stomach epithelum.
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