Bibliothek

feed icon rss

Ihre E-Mail wurde erfolgreich gesendet. Bitte prüfen Sie Ihren Maileingang.

Leider ist ein Fehler beim E-Mail-Versand aufgetreten. Bitte versuchen Sie es erneut.

Vorgang fortführen?

Exportieren
Filter
  • Chitinase Cell suspension  (1)
  • Homologous/heterologous hybridizations  (1)
  • 1
    ISSN: 1617-4623
    Schlagwort(e): Sex and male sterility differentiation ; Phytohormones ; Homologous/heterologous hybridizations ; Organ specificity/sexual genotype
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Summary Sequences specifically transcribed in each sex type of Mercurialis annua have been demonstrated by comparative analysis of their poly(A)+ RNA populations (homologous and heterologous hybridizations). A comparison of the curves for fertile male genotype cDNAs/fertile male genotype poly(A)+ RNAs and fertile male cDNAs/female genotype poly(A)+ RNAs clearly demonstrates that the staminate flowers of fertile male plants have 6.5% specific sequences without counterpart in poly(A)+ RNAs of the pistillate flowers of female genotypes. The poly(A)+ population of genetic females is composed primarily of amplified male transcripts [female cDNAs/male poly(A)+ RNAs, 100% hybridizations with the homologous curve of female cDNAs/female poly(A)+ RNAs]. Cytokinin reproduces the amplification of male transcripts in the course of artificial feminization of genetically male individuals and exogenous benzylaminopurine induces sequences specific for feminization. The poly(A)+ RNAs of the constructed sterile male strain and the restored fertile male strain present 11.5% and 9.0% specificity, respectively, with reference to staminate flowers of fertile males [sterile or restored fertile male cDNAs/fertile male poly(A)+ RNAs]. The existence of differential sequences even in identical organs (stamens in normal genetic male plants or restored fertile male strain, pistils in normal genetic females or constructed females bearing male sterility determinants) is clearly demonstrated and correlated with the determinant genotype of these sex types and with the hormones they contain.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    ISSN: 1617-4623
    Schlagwort(e): Abscisic acid ; cDNA cloning ; Chitinase Cell suspension ; Water stress
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract We have identified one osmotic stress- and abscisic acid-responsive member of the endochitinase (EC 3.2.1.14) gene family from leaves of drought-stressed Lycopersicon chilense plants, a natural inhabitant of extremely arid regions in South America. The 966-bp full-length cDNA (designated pcht28) encodes an acidic chitinase precursor with an amino-terminal signal peptide. The mature protein is predicted to have 229 amino acid residues with a relative molecular mass of 24 943 and pI value of 6.2. Sequence analysis revealed that pcht28 has a high degree of homology with class II chitinases (EC 3.2.1.14) from tomato and tobacco. Expression of the pcht28 protein in Escherichia coli verified that it is indeed a chitinase. Northern blot analysis indicated that this gene has evolved a different pattern of expression from that of other family members reported thus far. It is highly induced by both osmotic stress and the plant hormone abscisic acid. Southern blot analysis of genomic DNA suggested that the pcht28-related genes may form a small multigene family in this species. The efficiency of induction of the gene by drought stress, in leaves and stems, is significantly higher in L. chilense than in the cultivated tomato. It is speculated that, besides its general defensive function, the pcht28-encoded chitinase may play a particular role in plant development or in protecting plants from pathogen attack during water stress.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
Schließen ⊗
Diese Webseite nutzt Cookies und das Analyse-Tool Matomo. Weitere Informationen finden Sie hier...