The role of cardiolipin as an acyl donor in dog heart N-acylethanolamine phospholipid biosynthesis

N-Acylethanolamine phospholipids were produced from endogenous substrates with dog heart mitochondrial and microsomal preparations. With mitochondria the N-acyl group contained 13.8% linoleate, with microsomes only 3.6%. Cardiolipin comprised 18.5% of mitochondrial and 3.3% of microsomal lipid P and contained 93.7 and 72.4% linoleic acid, respectively. Incubation of dog heart subcellular fractions with [1-14C]linoleoyl cardiolipin in the presence of Ca2+ resulted in the formation of N-acylethanolamine phospholipids labeled primarily in the N-acyl and 1-O-acyl moieties. The data indicate that cardiolipin is the major source of linoleic acid used in the N-acylation of ethanolamine phospholipids by transacylase activity.     

Proacrosin and the differentiation of the spermatozoa

Using the indirect immunofluorescence staining technique, the occurrence and localization of proacrosin, the zymogen form of acrosin, was studied during spermatogenesis in the bull, ram, boar and rabbit. Proacrosin staining was demonstrable for the first time in the early haploid spermatid and increased with the differentiation of the spermatid to spermatozoon. The spermatozoon is covered by a cap-like structure of uniform fluorescence corresponding to the acrosomal compartment of the male gamete. No fluorescence could be found in diploid spermatogenic cells, i.e., in spermatogonia and spermatocytes. An identical developmental pattern of proacrosin was observed with the indirect immunoperoxidase staining technique. However, with this staining technique a distinct distribution of proacrosin staining was observed in the acrosome of epididymal and ejaculated spermatozoa of the bull, ram, boar, rabbit and man. Proacrosin seems to be distributed in the acrosome in granules rather than in the homogeneous form, as was indicated by the results of indirect immunofluorescence staining.     

Biosynthesis of N-acylethanolamine phospholipids by dog brain preparations

Abstract: Dog brain homogenates and subcellular preparations incubated in the presence of Ca²⁺ produced a new phospholipid that was isolated and identified by its infrared spectrum and by chemical degradation as a mixture of 1, 2-diacyl, alkenylacyl, and alkylacyl sn -glycero-3-phospho ( N -acyl)ethanolamines, 50, 45, and 5%, respectively. The N -acyl groups consisted almost exclusively of 16:0, 18:0, and 18:1 fatty acids. Formation of N -acylethanolamine phospholipids from endogenous substrates was linear for about 90 min at approximately 4.5 nmol/h/mg protein and exhibited a pH optimum of 10. Biosynthetic activity was associated with particulate fractions, primarily microsomes, synaptosomes, and mitochondria, but not with myelin. In each case, small amounts (∼0.5 nmol/h/mg protein) of long-chain N -acylethanolamines were also produced. Incubation of dog brain microsomes with 1,2-di[1'-¹⁴C]palmitoyl glycero-phosphocholine yielded N -acylethanolamine phospholipids labeled at both N -acyl (55%) and O -acyl (45%) moieties. It appears that dog brain organelles may contain a phosphatidylethanolamine N -acyl transferase (transacylase) analogous to that recently demonstrated in the myocardial tissue.     

De novo synthesis and specific assembly of keratin filaments in nonepithelial cells after microinjection of mRNA for epidermal keratin

Poly(A)+ RNA isolated from bovine muzzle epidermis was microinjected into nonepithelial cells containing only intermediate-sized filaments of the vimentin type. In recipient cells keratin polypeptides are synthesized and assemble into intermediate-sized filaments at multiple dispersed sites. We describe the time course and the pattern of de novo assembly of keratin filaments within living cells. These filaments were indistinguishable, by immunofluorescence and immunoelectron microscopic criteria, from keratin filament arrays present in true epithelial cells. The presence of extended keratin fibril meshworks in these injected cells is compatible with cell growth and mitosis. Double immunolabeling revealed that newly assembled keratin was not codistributed with microfilament bundles, microtubules or vimentin filaments. We suggest that assembly mechanisms exist which in vivo sort out newly synthesized cytokeratin polypeptides from vimentin.     

Chromosome banding in Amphibia

The mitotic and meiotic chromosomes of the marsupial frog Gastrotheca riobambae were analysed with various banding techniques. The karyotype of this species is distinguished by considerable amounts of constitutive heterochromatin and unusual, heteromorphic XY sex chromosomes. The Y chromosome is considerably larger than the X chromosome and almost completely heterochromatic. The analysis of the banding patterns obtained with GC- and AT-base-pair-specific fluorochromes shows that the constitutive heterochromatin in the Y chromosome consists of at least three different structural categories. The only nucleolus organizer region (NOR) of the karyotype is localized in the short arm of the X chromosome. This causes a sex-specific difference in the number of NOR: female animals have two NORs in diploid cells, male animals one. No cytological indications were found for the inactivation of one of the two X chromosomes in the female cells. In male meiosis, the heteromorphic sex chromosomes form a characteristic sex-bivalent by pairing their telomeres in an end-to-end arrangement. The significance of the XY/XX sex chromosomes of G. riobambae for the study of X-linked genes in Amphibia, the evolution of sex chromosomes and their specific DNA sequences, and the significance of the meiotic process of sex chromosomes are discussed.     

XX/XO-Mosaik bei einem männlichen Individuum mit Kleinwuchs und Hypospadie

Zusammenfassung Bei einem normal intelligenten, kleinwüchsigen, 219/12 jährigen Mann mit Hypospadie, fraglicher rudimentärer Vagina und hypergonadotropem Hypogonadismus findet man bei der Biopsie des nur 7 ml großen linken Hodens eine gleichförmige tubuläre Atrophie mit Fehlen des Keimepithels und eine diffuse, kleinherdige Leydigzellwucherung. Sex-Chromatin in den Leydigzellen, im Mundabstrich und Drumsticks negativ. Karyotyp in den Lymphocyten und im Knochenmark normal weiblich (46,XX), in den Fibroblasten jedoch 45,XO.Somit weist dieser Patient Testesgewebe auf, das Y-Chromosom ist aber unauffindbar. Zur Klärung dieser Diskrepanz scheint das Vorhandensein einer dritten, zahlenmäßig stark in den Hintergrund tretenden, ein Y enthaltenden Zellpopulation die naheliegendste Hypothese zu sein.Eine Zwillingsschwester kam im Neugeborenenalter ad exitum; die Blutgruppenuntersuchungen beim Patienten und seiner Familie machen aber einen Blutchimärismus sehr unwahrscheinlich.Das klinische Bild unseres Patienten ist vollkommen verschieden von demjenigen, das beim XX/XO-Mosaik üblicherweise beobachtet wird und läßt sich auch vom klassischen Klinefelter-Syndrom deutlich abgrenzen. Es zeigt Ähnlichkeiten mit einigen Fällen von XO/XY-Mosaik.

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Summary In a normally intelligent man of 219/12 years the following main physical findings were present: short stature, hypospadias, possibly a rudimentary vagina, hypergonadotropic hypogonadism, small testis (7 ml) with tubular dystrophy consisting in absence of germinal epithelium and localized proliferation of Leydig's cells. Sex chromatin in buccal mucosa cells was negative; no drumsticks were found in neutrophils. The karyotype in lymphocyte cultures and bone-marrow preparations was 46,XX; in several independent fibroblast cultures 45,XO.The most likely explanation for the presence of testicular tissue seems to be the existence of an undiscovered cell population containing a Y-chromosome.A twin sister of the patient died in early infancy; blood group investigations gave no indications for the presence of blood chimerism.The clinical picture of this patient is entirely different from that of the usual XX/XO mosaics, it also clearly differs from Klinefelter's syndrome but shows some similarities to cases of XO/XY mosaicism.

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Direktor: Prof. Chr. Hedinger     

Quantum Requirement for Photosynthesis in Chlorophyll-Deficient Plants with Unusual Lamellar Structures

Neither an over-all deficiency of chlorophyll, nor an increased enzymatic capacity for maximal rates, nor an unusual lamellar structure was found to change the number of quanta required for the evolution of one molecule of oxygen in healthy aurea mutants of tobacco. The average minimal quantum number remains 10 (efficiency 0.1) as in many algae and typical higher plants. Most of the time the optimal efficiency depends on the availability of some far-red radiation, particularly in the blue region of the spectrum where blue light alone is rather inefficient. These results fit an explanation offered earlier in connection with the hydrogen or acetate photometabolism of algae in far-red light.