Molecular genetic analysis of 67 patients with duchenne/becker muscular dystrophy

Summary A total of 56 Duchenne muscular dystrophy (DMD) patients and 11 Becker muscular dystrophy (BMD) patients was analyzed by extended multiplex amplification of the DMD/BMD gene; deletions were found in 60% of these patients. The data obtained were used to test the frameshift hypothesis and to compare the distribution of familial versus isolated cases. A significant correlation was found between deletions and isolated cases. Additional experiments were performed in order to determine the deletion breakpoints more precisely. These data are a prerequisite for carrier analysis in the respective families by detection or exclusion of aberrant cDNA fragments derived from ectopic lymphocyte RNA. This diagnostic technique is illustrated by 5 examples.     

Identification of the AMP binding sites of rabbit phosphofructo-1-kinase isozymes B and C

Rabbit liver phosphofructo-1-kinase, designated isozyme B, and rabbit brain phosphofructokinase, which contains all three isozymes as heteropolymers, have been modified by [14C]fluorosulfonylbenzoyladenosine (FSBAdo). Several lines of evidence supported modification at the binding site for AMP. The modification proceeded to the extent of 2 to 4 mol of reagent incorporated per mol of tetramer, and AMP protected against the reaction. The kinetic properties of modified isozymes A and B and of modified brain phosphofructokinase were examined and compared to their unmodified forms. It was observed that modification greatly diminished ATP inhibition of all of the isozymes. Furthermore, equilibrium binding studies of modified phosphofructokinase B showed a greatly diminished capacity and affinity for cyclic AMP. Cyclic AMP had little or no influence on the properties of modified A isozyme or brain phosphofructokinase, but was capable of further deinhibiting modified B isozyme, apparently at sites remaining unmodified by FSBAdo. Phosphofructokinase B, modified by radiolabeled FSBAdo, was digested by trypsin, and the digest separated by high-pressure liquid chromatography. The labeled peptide was isolated and sequenced to provide the sequence: Asn-Tyr-Gly-Thr-Lys-Leu-Gly-Val-Lys, with the lysine in the fifth position being the site of modification. To isolate isozyme C, a monoclonal antibody to this isozyme was produced by injecting purified rabbit brain phosphofructokinase into mice, and subsequently selecting for those clones that recognized brain phosphofructokinase but not purified phosphofructokinases A and B. The selected monoclonal was specific for native rabbit isozyme C and would not recognize mouse or rat brain phosphofructokinases. Linking the antibody to an inert phase provided an efficient means of purifying rabbit isozyme C from rabbit brain. The enzyme so recovered retained little of its original activity, but the method provided a simple technique for the preparation of enzyme for protein chemistry studies. The modified C isozyme was isolated on the immuno-affinity column and digested with trypsin. A tryptic peptide bearing the label was isolated and sequenced to provide the structure: Asn-Phe-Gly-Thr-Lys-Ile-Ser-Ala-Arg, with position 5 being the site of modification. The sequences of isozymes B and C are homologous to the site of modification of the A isozyme by FSBAdo.     

Spatial distribution of species diversity indices and their correlation with plot size

In a physiognomically uniform Leucobryo-Pineteum phytocoenose the spatial pattern of point diversity was determined and the effect of quadrat size on the assessment of alpha diversity (in Whittaker's, 1977, sense) was analysed. In both cases the Shannon index of total species diversity and the evenness index were used to measure diversity. A contagious spatial pattern of point diversity and a high variation of point diversity values, as well as a strong non-linear dependence of H and J values on quadrat size, and also a decrease in H and J variation with an increase in quadrat size were found.Nomenclature follows Ehrendorfer (1973). Liste der Gefässpflanzen Mitteleuropas.     

Biological role of endoreplication in the process of spermatogenesis inChara vulgaris L.

Summary During cell division in antheridial filaments ofChara vulgaris an increase in DNA content occurs in both shield cells and manubria within an antheridium, reaching 16C–64C and 8C–32C levels, respectively. Endoreplication ceases prior to the formation of spermatids and initiation of spermiogenesis, probably as a result of symplasmic isolation of the antheridium from the thallus. As the DNA content of the nuclei increases, the shield cells³H-leucine incorporation increases, and they grow intensively in the tangential plane. Translation decreases considerably after termination of shield cell growth. DNA content of mature manubria is half of that in shield cells, although their size is 10 times that of manubria. Translational activity of manubria also increases as DNA content rises and cells grow. However, during spermiogenesis, this activity remains at its maximum, which is associated with the secretory function of the manubria. Spermiogenesis is also accompanied by far-reaching ultrastructural changes within the manubrial cytoplasm.The level of endopolyploidy in both shield cells and manubria of antheridia formed in the spring is higher by one replication cycle, than in autumnal antheridia. AMO-1618, at a concentration of 10^–5M reduces the DNA content in the autumnal manubria. The higher the manubrial level of endopolyploidy in spermiogenesis, the greater their size, and the higher the translational activity and number of joined spermatids. The number of spermatozoids in the antheridium is also positively correlated with the internal volume of an antheridium, which is itself dependent on the endopolyploidy level of shield cells.The results obtained confirm the assumption that endoreplication favours the higher growth dynamics and potential translational activity, which occurs in the dynamic growth phase only in shield cells, while in manubria, i.e. cells producing substances necessary to spermatozoids development, it remains high until the end of spermiogenesis.     

THE RELATIONSHIPS BETWEEN THE PRIMARY VASCULAR SYSTEM AND PHYLLOTACTIC PATTERNS OF ANAGALLIS ARVENSIS (PRIMULACEAE)

The various primary vascular systems of shoots of Anagallis arvensis L. (Primulaceae) can be distinguished in relation to the number of leaves (two, three, or four) at each node. In this study, shoot segments (single intemodes and the nodes above them) were examined. The arrangement of segments within shoots was also recorded. The vasculature forms a closed system with the number of sets of bundles usually equal to twice the number of leaves. Irregularities are found in the following features of the system: the number of bundles composing leaf half-traces; occurrence of anastomosing bundles; the number of intemodes through which bundles extend; levels of leaf attachment to the stem at the node; and distribution of parenchyma within the vascular cylinder, which determines the number of bundles in sets and the number of bundle sets. The irregularities occur with different frequencies for segments exhibiting different phyllotactic patterns. Comparison of these frequencies leads to the following conclusions: anastomosing bundles occur only in decussate or trimerous shoot segments, whereas sets of bundles united within intemodes and displaced leaves occur only in tetramerous or trimerous ones; decrease of the number of bundles per leaf and displacement of leaves at the nodal level are correlated; variation between segments exhibiting the same phyllotactic pattern is greatest for trimerous, less for tetramerous, and least for decussate segments; the vascular system of decussate shoot segments is more stable than that of the other systems; and trimerous segments seem to be intermediate between the other two segment types.     

Changes in the content of condensed chromatin during the cell cycle in antheridial filaments ofChara vulgaris L. as related to DNA and RNA synthesis,3H actinomycin D binding and RNA polymerase activity

Summary Using light microscopic autoradiography it was found that in the middle S and G₂ phases of the cell cycle in antheridial filaments (S + G₂ + M type) ofChara vulgaris L., an intensified RNA synthesis took place. The process was correlated with enhanced binding of³H actinomycin D to the DNA template, increased RNA polymerase activity, and enhanced chromatin decondensation.This work was supported by the Polish Academy of Sciences within the project 09.7.3.1.4.     

Localization of neurosecretion in the nervous system of Catenulida (Turbellaria)

Summary The nervous system of the most primitive fresh-water Turbellaria of the order Catenulida was investigated. Neurosecretory cells were found to occur in it. These cells have a structure similar to that of nerve cells, they only differ by the presence of neurosecretion granules and a more developed golgi complex. In the simplest Catenulida,Stenostomun, neurosecretory granules are found both in the brain cells and in the trunks in the nerve fibres where they are rather randomly distributed. Another representative of this family, the more highly organizedCatenula, exhibits specialized brain and nerve trunk regions containing neurosecretion granules. This work was supported in part by the Committee on Cytobiology of the Polish Academy of Sciences     

Actin-binding proteins involved in the capping of epidermal growth factor receptors in A431 cells.

A capping process of epidermal growth factor receptors (EGF-Rs) was used for the study of the relation between the receptors and the actin-binding proteins (spectrin, vinculin, annexin I) that may be involved in EGF-R-cytoskeleton interaction. In intact, adherent A431 cells, EGF-Rs were diffusively distributed on the cell surface. Spectrin, vinculin, and annexin I were located beneath the plasma membrane. An abundance of EGF-Rs as well as submembrane proteins was observed in regions of membrane ruffles and cell-cell contacts. Annexin I was localized also in cytoplasm being attached to filamentous structures surrounding the nucleus and extending to the cell periphery. Under polyvalent ligand treatment, EGF-Rs of adherent cells were aggregated on one side of the cell. Spectrin, vinculin, and annexin I dislocated together with EGF-Rs and were concentrated under plasma membrane at regions where cap formation took place. In suspended A431 cells only spectrin was located under the plasma membrane whereas annexin I and vinculin were diffusively distributed through the cells. During cap formation only spectrin was colocalized with EGF-Rs. The results confirmed the major role of spectrin as a receptor-microfilament linking protein.