Nucleolar binding sequences of the ribosomal protein S6e family reside in evolutionary highly conserved peptide clusters

Proteomic analyses of the nucleolus have revealed almost 700 functionally diverse proteins implicated in ribosome biogenesis, nucleolar assembly, and regulation of vital cellular processes. However, this nucleolar inventory has not unveiled a specific consensus motif necessary for nucleolar binding. The ribosomal protein family characterized by their basic nature should exhibit distinct binding sequences that enable interactions with the rRNA precursor molecules facilitating subunit assembly. We succeeded in delineating 2 minimal nucleolar binding sequences of human ribosomal protein S6 by fusing S6 cDNA fragments to the 5' end of the LacZ gene and subsequently detecting the intracellular localization of the beta-galactosidase fusion proteins. Nobis1 (nucleolar binding sequence 1), comprising of 4 highly conserved amino acid clusters separated by glycine or proline, functions independently of the 3 authentic nuclear localization signals (NLSs). Nobis2 consists of 2 conserved peptide clusters and requires the authentic NLS2 in its native context. Similarly, we deduced from previous publications that the single Nobis of ribosomal protein S25 is also highly conserved. The functional protein domain organization of the ribosomal protein S6e family consists of 3 modules: NLS, Nobis, and the C-terminal serine cluster of the phosphorylation sites. This modular structure is evolutionary conserved in vertebrates, invertebrates, and fungi. Remarkably, nucleolar binding sequences of small and large ribosomal proteins reside in peptide clusters conserved over millions of years.     

Reduced Basal ATP Synthetic Flux of Skeletal Muscle in Patients with Previous Acromegaly

Background

Impaired mitochondrial function and ectopic lipid deposition in skeletal muscle and liver have been linked to decreased insulin sensitivity. As growth hormone (GH) excess can reduce insulin sensitivity, we examined the impact of previous acromegaly (AM) on glucose metabolism, lipid storage and muscular ATP turnover.

Participants and Methods

Seven AM (4f/3 m, age: 46±4 years, BMI: 28±1 kg/m²) and healthy volunteers (CON: 3f/4 m, 43±4 years, 26±2 kg/m²) matched for age and body mass underwent oral glucose testing for assessment of insulin sensitivity (OGIS) and ß-cell function (adaptation index, ADAP). Whole body oxidative capacity was measured with indirect calorimetry and spiroergometry. Unidirectional ATP synthetic flux (fATP) was assessed from ³¹P magnetic resonance spectroscopy (MRS) of calf muscle. Lipid contents of tibialis anterior (IMCLt) and soleus muscles (IMCLs) and liver (HCL) were measured with ¹H MRS.

Results

Despite comparable GH, insulin-like growth factor-1 (IGF-I) and insulin sensitivity, AM had ∼85% lower ADAP (p<0.01) and ∼21% reduced VO₂max (p<0.05). fATP was similarly ∼25% lower in AM (p<0.05) and related positively to ADAP (r = 0.744, p<0.01), but negatively to BMI (r = −0.582, p<0.05). AM had ∼3fold higher HCL (p<0.05) while IMCLt and IMCLs did not differ between the groups.

Conclusions

Humans with a history of acromegaly exhibit reduced insulin secretion, muscular ATP synthesis and oxidative capacity but elevated liver fat content. This suggests that alterations in ß-cell function and myocellular ATP production may persist despite normalization of GH secretion after successful treatment of acromegaly.     

Über die Sehschärfe der Elritze (Phoxinus laevis) Bei verschiedenen Helligkeiten

Zusammenfassung Zwischen Sehschärfe und Beleuchtungsintensität bestehen bei den Fischen kurz folgende Beziehungen: Die Sehschärfe der Elritze wächst ungefähr proportional dem Logarithmus der Beleuchtungsstärke. Ihr Maximum ist bei einer relativ geringen Helligkeit erreicht. Der Übergang vom Tages-zum Dämmerungssehen ist durch eine Änderung der Sehschärfe gekennzeichnet, die bei der Elritze — umgekehrt wie beim Menschen — im Bereich des Stäbchensehens eine etwas schnellere Abnahme erfährt als im Bereich des Zapfensehens.     

Ein Beitrag zur Züchtung vonDigitalis lanata Ehrh

Ohne ZusammenfassungMit 2 AbbildungenFrau Professor Dr.E. Schiemann zum 80. Geburtstag gewidmet.     

Splenic haematopoiesis in primary (idiopathic) osteomyelofibrosis: immunohistochemical and morphometric evaluation of proliferative activity of erythro- and endoreduplicative capacity of megakaryopoiesis (PCNA- and Ki-67 staining)

Using monoclonal antibodies against proliferating cell nuclear antigen or PCNA (PC10) and the Ki-67 antigen (MIB1), an immunohistological and morphometric study was performed on routinely processed splenic tissue from ten patients with primary (idiopathic) osteomyelofibrosis (OMF). To determine the proliferation capacity of erythroid precursors and the endoreduplicative activity of megakaryocytes, corresponding antibodies (Ret40f and CD61) were applied in combination with the cell-cycle markers (sequential double-immunostaining). Morphometric analysis revealed no significant differences in PCNA or Ki-67 reactivity in either cell lineages. In comparison with previous studies on normal bone marrow, in splenic tissue showing myeloid metaplasia, the numbers of PCNA-labelled proerythroblasts, erythroblasts and megakaryocytes were conspicuously increased. Considering the ineffective erythropoiesis in OMF, there seemed to be a disproportional enhancement in PCNA and Ki-67 immunostaining of the red cell lineage. Similarly, the small size of megakaryocytes in advanced, OMF-associated myeloid metaplasia was in keeping with an impairment of endoreduplicative activity. In addition to various other contributory factors, anaemia in OMF may be partially caused by secondary folate (haematinic) deficiency. From experimental studies this defect is known to cause an abnormal arrest in the S-phase of the cell-cycle, comparable to that characterising pernicious anaemia. As a sequel of this pathomechanism, an undue overexpression of PCNA and Ki-67 has to be assumed, that is not necessarily associated with DNA synthesis or cell cycling. This work was supported by a grant from the Deutsche Forschungsgemeinschaft (DFG-Th 390/1-3)     

Ranunculus penicillatus in Norden

Twenty-one populations of Ranunculus subgenus Batrachium (Ranunculaceae) from central Jutland, Denmark, were studied in the field and sampled for cytological, morphological and embryological investigation; for embryology the confocal laser scanning method (CLSM) was used. Six taxa were represented: R. penicillatus ssp. penicillatus and ssp. pseudofluitans, R. aquatilis var. aquatilis, R. peltatus ssp. peltatus and ssp. baudotii and R. circinatus . The main aim was to determine whether R. penicillatus occurs in the area. 14 of the 21 populations were referred to R. penicillatus; all 14 were tetraploid, though a few triploid plants were also found in two of these populations. Some populations show characteristic features of hybrid origin. These have, however, found a niche in swift rivers in west-central Jutland, reduction in fertility being compensated for by the dominant asexual mode of reproduction, and new parts of the river systems have continually been invaded. They are accorded taxonomic rank, the heterophyllous populations being treated as ssp. penicillatus and the homophyllous populations as ssp. pseudofluituns . Accordingly, R. penicillatus is represented in Denmark and thus in Norden. Flora Nordica Notes no. 7.     

Cloning and sequence analysis of the 18 S ribosomal RNA gene of tomato and a secondary structure model for the 18 S rRNA of angiosperms

Summary The gene of a cytoplasmic 18 S ribosomal RNA (18 S rDNA) of the dicotyledonous plant tomato (ycopersicon esculentum) cv. Rentita has been cloned, and its complete primary structure has been determined. The tomato 18 S rDNA is 1805 by long with a G+C content of 49.6%. Its sequence exhibits 94%–96% positional identity when it is colinearly aligned with the previously reported sequences of the 17–18 S rDNAs of the dicot soybean and the monocots maize and rice. A model of the secondary structure of the 18 S rRNA of angiosperms is presented and its genera-specific structural features are compared with a current eukaryotic 18 S rRNA consensus model.     

Experiments on wavelength specific behavior ofPieris brassicae L. During drumming and egg-laying

Summary Female cabbage white butterflies, under constant laboratory conditions exhibit wavelength specific behavior in choosing sites for egg-laying and drumming.In preliminary spontaneous choice experiments with colored PVC-sheets (Table 1, results) butterflies gave somewhat different preference order than with monochromatic lights of different wavelength but equal relative quantum flux (Table 2A, B). These differences probably depended on the relative number of quanta and the spectral composition of the light reflected by the sheets.White light is ignored by the butterflies during both drumming and egg-laying, up to intensities 60 times that of the monochromatic light stimulus.The functional categories egg-laying and drumming are both associated with the spectral region from 497 nm to ca. 585 nm (Fig. 10). The functional category feeding reaction is associated with regions adjoining that for egg-laying and drumming on both the shorter-wavelength side (<497nm) and the longer-wavelength side (>578nm).Wavelength specific behavior and the significance of odor substances in the chain of stimuli that lead up to egg-laying are discussed.Respectfully dedicated to Prof. H. Autrum on the occasion of his 75th birthdaySupported by the Deutsche Forschungsgemeinschaft     

Immunohistochemical identification of T- and B-lymphocytes delineated by the unlabelled antibody enzyme method

Summary T-lymphocytes and B-lymphocytes are identified in tissue sections of human tonsils by applying the unlabelled antibody enzyme method. The epithelium of the tonsils contains a majority of immunoglobulin-positive cells and fewer T-lymphocytes. In the subepithelial zones, areas composed of B-cells predominate, however, regions containing T-lymphocytes are also present. The latter are mainly arranged in the lamina propria around high-endothelial venules and often include plasma cells containing immunoglobulin. Follicles containing germinal centres display a complex structure which changes during development. The lymphocytic cap consists of densely packed lymphocytes, labelled heavily by anti-IgM and anti-IGD, and of individual T-lymphocytes. Germinal centres show a framework of immunoglobulin-positive dendritic reticular cells; they contain some heavily labelled lymphoid cells and several cells weakly labelled by anti-IgM and anti-IgA, as well as a small number of T-lymphocytes. Furthermore, the total areas of T- and B-lymphocytes measured by planimetry may differ considerably between different tonsils. Especially total areas of germinal centres vary to a great extent. The quantitative data on amounts of T- and B-cells achieved by planimetry are comparable to those reported in cellular suspensions of tonsils.