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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 74 (1987), S. 125-139 
    ISSN: 1432-2242
    Keywords: Vicia faba ; Chloroplast genomic evolution ; Rearrangements ; Recombination sites ; Deletions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The Vicia faba chloroplast genome lacks inverted repeat sequences and contains only one set of ribosomal RNA genes. The genetic organization has been altered by inversions, relative to the typical arrangement of most higher plant chloroplast genomes. The Vicia faba plastid genome thus represents one of the more interesting results of chloroplast genomic evolution. The present study employs small DNA probes and Southern blot hybridizations to investigate the steps involved in the evolution of the Vicia faba chloroplast genome. The data from heterologous hybridizations between chloroplast DNA of Brassica napus (a conserved genome) and of Vicia faba led to three observations: 1) The inverted repeat segment closest to the psbA gene was deleted prior to the rearrangements. 2) A quarter of the ancestral small single copy region was lost during the deletion. 3) The genetic organization observed in Vicia faba resulted from three inversions after the deletion event. Our findings, combined with previous observations, helped devise a stepwise model for the evolution of the Vicia faba chloroplast genome. The area of the small single copy region absent from the Vicia faba chloroplast chromosome lacks in vivo transcription activity in Brassica napus.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-136X
    Keywords: Anion movements ; Chloride/bicarbonate exchange ; Red cell proteins ; AE1 or band 3 ; Petromyzon marinus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Physiological and immuno-blotting experiments were used to determine whether the red blood cell membrane of a primitive vertebrate, the sea lamprey Petromyzon marinus, contained a counterpart similar to the vertebrate anion exchange protein known as AE1 or band 3. Results of the physiological experiments which measured CO2 production after adding H14CO 3 - to the extracellular saline, indicated significant transmembrane bicarbonate movement in lamprey blood which unlike that in most vertebrates, was insensitive to inhibition by 4,4′ diisothiocyanatostilbene-2,2′ disulfonic acid. The present study also showed that lamprey red blood cells possess acetazolamide-sensitive carbonic anhydrase which is an important component of CO2 production by vertebrate red blood cells. Polyclonal immunoglobulins against a 12 amino acid domain in the C-terminus of the mouse AE1 recognized a trout red blood cell membrane protein with a relative molecular mass of 97 kDa, but failed to immunoreact with any membrane proteins from the red blood cells of lamprey. Antibodies against trout AE1 immunoreacted with trout red blood cell membrane proteins of approximately 97 kDa, 200 kDa and 〉200 kDa. Interestingly, only a 200-kDa membrane protein from the red blood cells of the primitive lamprey immunoreacted with the trout anti-AE1 immunoglobulin proteins. Therefore, lamprey red blood cells appear to possess an AE1-like protein that may be physiologically different than that in most other vertebrates.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Neurological sciences 16 (1995), S. 91-99 
    ISSN: 1590-3478
    Keywords: GEPR ; Genetically Epilepsy-Prone Rats ; seizures ; epilepsy ; forebrain seizure ; brainstem seizure ; electroencephalography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Sommario Due ceppi indipendenti di ratti geneticamente suscettibili ad epilessia (GEPRs) sono stati ottenuti mediante reincroci. GEPR-3s e GEPR-9s differiscono per il grado di predisposizione alle crisi della loro espressione rispettivamente moderato e importante. La predisposizione alle crisi stabilisce una distinzione fondamentale tra cervello normale ed epilettico. Sia nei GEPRs che nell'uomo la predisposizione alle crisi riguarda sia le crisi spontanee sia il grado di responsività o la soglia di risposta a stimoli che possono causare crisi anche in soggetti non epilettici. L'attivazione di circuiti epilettogeni del tronco da parte dell'input uditivo, attraverso il collicolo inferiore, provoca nei GEPR-9s risposte elettrografiche e comportamentali che riproducono le crisi generalizzate tonico-cloniche dell'uomo. L'attivazione dei circuiti epilettogeni del tronco da parte di circuiti epilettogeni proencefalici nei GEPRs rappresenta un modello recentemente individuato di crisi parziali complesse con generalizzazione secondaria a crisi tonico-cloniche. Per questi motivi la predisposizione epilettica nei GEPRs rappresenta una opportunità privilegiata per lo studio delle epilessie umane non riscontrabile in studi sul cervello normale esposto a stimoli epilettogeni.
    Notes: Abstract Two independently inbred strains of genetically epilepsy-prone rats (GEPRs) have been developed. GEPR-3s and GEPR-9s have moderate and severe degrees of seizure predisposition as well as expression, respectively. Seizure predisposition is a fundamental distinction between the normal and epileptic brain. Seizure predisposition in GEPRs and in humans with epilepsy includes spontaneous seizures and exaggerated seizure responsiveness and/or abnormally low thresholds to stimuli which also cause seizures in non-epileptic subjects. Activation of brainstem seizure circuitry by auditory input via the inferior colliculus causes electrographic and behavioral responses in GEPR-9s which replicates human generalized tonic/clonic seizures. Activation of brainstem seizure circuitry by input from forebrain seizure circuitry in GEPRs provides a newly discovered model of complex partial seizures with secondary generalization to tonic/clonic seizures. Thus, seizure predisposition in GEPRs offers a unique opportunity to study the human epilepsies that is not offered in studies of normal brain exposed to convulsant stimuli.
    Type of Medium: Electronic Resource
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