High frequency of-β-hexosaminidase deficiency in lymphoblastoid cell lines

The activity of seven lysosomal enzymes was determined in 25 lymphoblastoid cell lines. These lines included normal controls transformed with Epstein-Barr virus, Burkitt's lymphomas and other lymphomas with or without EBV genome.Four lines were deficient in total β-hexosaminidase activity. The deficiency was as severe as that of the variant O (Sandhoff's disease) of clinical β-hexosaminidase deficiency. The electrophoretic pattern was also similar to that observed in Sandhoff's disease.The possible mechanisms explaining the high frequency of β-hexosaminidase deficiency in lymphoblastoid cell lines are discussed.     

Actin microfilaments and fibroin secretion in the silkgland cells of Bombyx mori : Effects of cytochalasin B

Bombyx mori posterior silkgland cells exhibit an impressive microfilament apparatus located at the cellular apex. It consists of bundles of packed, long microfilaments of 50–70 Å diameter running along circumferences delimiting the lumen of the gland, perpendicularly to the flow of luminal silk. Microfilaments are closely associated with microtubules of the cytoplasmic ‘radial microtubule system’. Immunolabelling with purified antihuman actin antibodies was used to demonstrate their actin-like nature. Apical microfilaments are sensitive to cytochalasin B (CB) which selectively inhibits the secretion of fibroin. Following the removal of the drug, microfilaments recover their normal morphology and secretion resumes. The possible implication of contraction of microfilaments in the process of secretion is discussed.     

Characterization and Complexity of Wheat Developing Endosperm mRNAs

Free and membrane-bound (MB) polysomes and the corresponding polyadenylated RNAs (polyA⁺ RNAs) have been isolated from developing wheat endosperm (Triticum aestivum L.) Free and MB poly(A)⁺ RNAs, analyzed on isokinetic sucrose gradient with [³H]polyuridylic acid [poly(U)] hybridization detection, appear to be 11S to 12S in size with a 7% poly(A) tail for MB RNAs. cDNAs synthesized using both of these mRNA populations in presence of a potent RNase inhibitor (RNasin), have been used for hybridization kinetics experiments. The mean square fitting analysis of the hybridization kinetics between MB cDNA and its template reveals the presence of two abundance classes representing roughly ⅔ and ⅓ of the MB poly(A)⁺ RNAs and containing the information for approximately 75 superabundant species (21,000 copies per cell) and 750 intermediate species (530 copies per cell), respectively. The mRNA population extracted from free polysomes is divided into three abundance classes. The first one is composed of superabundant sequences which would correspond to the MB superabundant mRNAs. The free mRNAs consist of about 11,000 diverse sequences, most of them being rare sequences. Heterologous hybridizations of MB cDNAs to free mRNAs have shown that some mRNAs are common to both populations. This could be explained either by a partial contamination or by free polysomes en route to their membrane destination. Contrary to the low number of diverse mRNAs corresponding to the legume seed storage proteins, the wheat endosperm superabundant mRNAs consist of about 75 different sequences which would encode most of the seed storage proteins, especially gliadins.     

In vivo isolation of a pPJ3a-λ cosmid mediated by the Tn2307 transposon

From an E. coli cell harboring plasmid pPJ3b (= pPJ3a::Tn2301) and infected with phage λ, we have isolated two defective phages having inserted pPJ3a DNA and Tn2301 in their genomes. One of them has been extensively characterized: it behaves like a cosmid, i.e., upon injection into the cell, its DNA circularizes and replicates as a plasmid (pPJ10); it can be packaged again in λ heads, provided the presence of a phage helper. Furthermore, heteroduplex analysis has shown that in pPJ10, the transposon Tn2301 is inverted compared to its direction in pPJ3b. We give evidence suggesting that this type of inversion is in part mediated by Tn2301.     

Régulation de la biosynthèse de l'aspartate-ammonium lyase (aspartase) de Pseudomonas fluorescens

Variations in aspartasic activity in various media are due to aspartate-ammonium lyase induction and to regulation of the biosynthesis of this enzyme. Evidence for neosynthesis of the enzyme is provided by labelling and separation of the protein. The inducer appears to be aspartic acid. The biosynthesis is subject to pronounced catabolic repression. The physiological function of aspartate-ammonium lyase is discussed.     

Methyl-4 formyl-7 cyclopenta(c)pyranne isole apres hydrolyse acide de Viburnum tinus

Viburtinal (4-methyl-7-formylcyclopenta(c)pyrane), yet unknown, was obtained by acid hydrolysis of the esters extracted from Viburnum tinus. Its structure was deduced by spectroscopic methods.     

Evolution de la musculature desNéréidiens (Annélides polychètes) au cours de l'Epitoquie

Résumé Au cours de l'épitoquie des Nereidiens, les fibres musculaires longitudinales ne sont pas forméesde novo, à partir de cellules indifferenciées ou myoblastes, mais proviennent des fibres anciennes atoques. Celles-ci subissent une véritable dédifférenciation plus ou moins synchrone d'une redifférenciation. Les deux processus ne sont pas successifs mais simultanés, et une dédifférenciation complète est absente.Les premières cellules en évolution appartiennent à la couche musculaire externe; ensuite, les fibres des assises plus profondes se transforment à leur tour.Les transformations consistent en: 1) La dédifférenciation du bord interne ou coelomique de la fibre. Les structures contractiles disparaissent dans cette zone et de nombreuses particules de glycogène se différencient sans relation avec le reticulum endoplasmique ou les ribosomes. Aucun lysosome ou signe précurseur ne peuvent être observés avant la disparition des filaments contractiles et des éléments Z. 2) Le bord coelomique s'hypertrophie. Dans la région axiale de la fibre, de nombreuses mitochondries et particules et de glycogène remplacent le matériel contractile. Corrélativement, l'épaisseur des bandes A et I diminue. 3) La fibre hétéronéreidienne ou épitoque est constituée et présente deux parties: un cortex myoplasmique et une médulla sarcoplasmique, remplie de mitochondries et de glycogène. Le noyau renfermant un nucléole volumineux est situé dans une hernie sarcoplasmique latérale.

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Evolution of muscles inNereidae (Annelida polychaeta) during Epitoky. III. Dedifferentiation of the longitudinal fibres

Summary During epitoky inNereidae, the longitudinal muscle fibres are not formedde novo from undifferentiated cells or myoblasts, but arise from the old atokous fibres. These undergo a true dedifferentiation more or less synchronously with a redifferentiation. The two processes are not successive but simultaneous and there is no complete dedifferentiation.The first cells that develop are in the outside muscle layer; then the fibres of the inside layers are transformed in their turn.The transformations consist of: 1) Dedifferentiation of the edge of the inner or coelomic fibre. The contractile structures disappear in this part and numerous glycogen particles differentiate, unrelated to endoplasmic reticulum or ribosomes. No lysosomes or precursory markings are observed before the disappearance of contractile filaments and Z rods. 2) The coelomic edge becomes enlarged. In the axial region of the fibre, numerous mitochondria and and glycogen particles take the place of the contractile material. Consequently, the thickness of A and I bands decreases. 3) The heteronereid or epitokous fibre is formed and shows two parts: a myoplasmic cortex and a sarcoplasmic medulla, filled with mitochondria and glycogen. The nucleus with a voluminous nucleolus settles inside a lateral sarcoplasmic swelling.

     

Regioelectronic factors in metabolic hydroxylation of aliphatic carbon atoms

EHT calculations have been performed on model molecules acting as substrates for mammalian mono-oxygenases. C_α---H bonds are consistently found to have larger overlap populations compared with C_β---H and C_γ---H bonds. It is known on the other hand that metabolic hydroxylation of aliphatic carbon atoms shows a marked regioselectivity for α-carbons. The quantum-mechanical results sustain the view that C---H bonds of relatively high electronic density are preferred target sites for the cytochrome P-450-mediated oxygenation, and that the oxygen atom being activated is transformed into an electrophilic species capable of C---H bond insertion.