Regulation of VL30 gene expression by activators of protein kinase C

The mouse genome contains a retrovirus-like sequence, designated VL30, which is expressed at high levels in transformed cells and which can be induced by exogenously supplied epidermal growth factor (EGF). Binding of EGF to the EGF receptor produces changes in intracellular calcium levels and phospholipase activity which indirectly lead to activation of protein kinase C. We treated AKR-2B cells, Swiss 3T3 cells, and the 3T3 variants NR6 (EGF receptorless) and TNR9 (phorbol ester nonresponsive) with various phorbol ester tumor promoters and with the synthetic diacylglycerol sn-1,2-dioctanoylglycerol. Tumor-promoting phorbol esters (e.g. 12-O-tetradecanoyl phorbol acetate (TPA] increased the level of VL30 expression. Stimulation with either TPA or EGF produced a similar time course of VL30 expression. TPA induced VL30 expression in the EGF-receptorless NR6 cell line, indicating that neither EGF ligand-receptor binding nor phosphorylation of the EGF receptor was required for induction of VL30 expression. Protein synthesis was not required for the TPA-mediated increase in VL30 expression, as pretreatment with cycloheximide did not block or reduce the TPA effect. VL30 expression was also stimulated by treatment with sn-1,2-dioctanoylglycerol, an analog of a probable endogenous activator of protein kinase C. These results suggest that activation of protein kinase C plays a direct role in regulating VL30 expression.     

Organization of the ribosomal ribonucleic acid genes in various wild-type strains and wild-collected strains of Neurospora

Summary The organization of the ribosomal DNA (rDNA) repcat unit in the standard wild-type strain of Neurospora crassa, 74-OR23-1A, and in 30 other wild-type strains and wild-collected strains of N. crassa, N. tetrasperma, N. sitophila, N. intermedia, and N. discreta isolated from nature, was investigated by restriction enzyme digestion of genomic DNA, and probing of the Southern-blotted DNA fragments with specific cloned pieces of the rDNA unit from 74-OR23-1A. The size of the rDNA unit in 74-OR23-1A was shown to be 9.20 kilobase pairs (kb) from blotting data, and the average for all strains was 9.11+0.21 kb; standard error=0.038; coefficient of variation (C.V.)=2.34%. These data indicate that the rDNA repeat unit size has been highly conserved among the Neurospora strains investigated. However, while all strains have a conserved HindIII site near the 5 end of the 25 S rDNA coding sequence, a polymorphism in the number and/or position of HindIII sites in the nontranscribed spacer region was found between strains. The 74-OR23-1A strain has two HindIII sites in the spacer, while others have from 0 to at least 3. This restriction site polymorphism is strain-specific and not species-specific. It was confirmed for some strains by restriction analysis of clones containing most of the rDNA repeat unit. The current restriction map of the 74-OR23-1A rDNA repeat unit is presented.     

Ribosomal genes of Neurospora crassa: constancy of gene number in the conidial and mycelial phases, and homogeneity in length and restriction enzyme cleavage sites within strains

We report the results of experiments which, while not specifically designed to study the possibility of rDNA amplification during different developmental stages in the N. crassa life cycle, clearly indicate a relative constancy in the rDNA content of conidia (asexual spores) and mycelial cells. We also report the results of restriction enzyme studies which indicate that the Neurospora rDNA repeat units are homogeneous in length and restriction site pattern within any given Neurospora strain. These results directly contradict the recent report of Dutta et al. (1983), in which the authors concluded that the rDNA of germinating conidia is amplified, relative to mycelia, and that up to 10% of the rDNA units are heterogeneous.     

Comprehensive proteomic analysis of human cervical-vaginal fluid

Cervical-vaginal fluid (CVF) is a potential rich source of biomarkers for enhancing our understanding of human parturition and pathologic conditions affecting pregnancy. In this study, we performed a comprehensive survey of the CVF proteome in pregnancy utilizing multidimensional liquid chromatography (2D-LC) coupled with mass spectrometry and gel-electrophoresis-based protein separation and identification. In total, 150 unique proteins were identified using multiple protein identification algorithms. Metabolism (32%) and immune response-related (22%) proteins are the major functional categories represented in the CVF proteome. A comparison of the CVF, serum, and amniotic fluid proteomes showed that 77 proteins are unique to CVF, while 56 and 17 CVF proteins also occur in serum and amniotic fluid, respectively. This data set provides a foundation for evaluation of these proteins as potential CVF biomarkers for noninvasive diagnosis of pregnancy-related disorders.     

Phosphatidylinositol 3-kinase-dependent,MEK- independent proliferation in response to CaR activation

Although ovarian surface epithelial(OSE) cells are responsible for the majority of ovarian tumors, we knowrelatively little about the pathway(s) that is responsible forregulating their proliferation. We found that phosphatidylinositol3-kinase (PI3K) is activated in OSE cells in response to elevatedextracellular calcium, and the PI3K inhibitors wortmannin and LY-294002inhibited extracellular signal-regulated kinase (ERK) activation by~75%, similar to effects of the mitogen-activated protein kinase/ERK kinase inhibitor PD-98059. However, in assays of proliferation, we found that PD-98059 inhibited proliferation by ~50%, whereas wortmannin inhibited >90% of the proliferative response to elevated calcium. Expression of a dominant negative PI3K totally inhibited ERKactivation in response to calcium. These results demonstrate that ERKactivation cannot account for the full proliferative effect of elevatedcalcium in OSE cells and suggest the presence of an ERK-independent,PI3K-dependent component in the proliferative response.

     

Regulation of ribosomal RNA cistron number in a strain of Neurospora crassa with a duplication of the nucleolus organizer region

Some progeny from a cross of the translocation mutant T(VL→IVL)AR33 with wild-type Neurospora crassa are double nucleolus organizer (DNO) strains, usually displaying two distinct nucleolus organizer regions. The DNO strain is sterile but displays the same growth response as normal laboratory strains of Neurospora. We used DNA-DNA hybridization techniques to quantify the number of rRNA cistrons in the DNO mutant and its vegetative progeny. Comparisons of the rate of hybridization of genomic DNA from the parental AR33 strain and from the DNO strain showed that hybridization was more rapid for the DNO strain than for the parental strain. Successive vegetative progeny of the DNO strain displayed hybridization rates intermediate to those of the original DNO strain and the parental single nucleolus strain, indicating that the number of rRNA cistrons had decreased during vegetative propagation. Estimates of rRNA cistron number obtained from comparisons of the amount of single copy DNA and rDNA hybridized to genomic DNO and AR33 DNA at saturation indicate that the parental AR33 strain contains 225 copies of the rRNA repeat unit, while the DNO strain has approx. 440 copies. The number of rRNA cistrons decreases gradually in the successive vegetative progeny, approximating the parental haploid value by the eleventh vegetative transfer.     

Changes in gape frequency, siphon activity and thermal response in the freshwater bivalves Anodonta cygnea and Margaritifera falcata

Physiologically-driven rhythms in bivalve molluscs are predictedto vary as a function of metabolic rate and temperature, incontrast to genetically predisposed biological clocks. Theserhythms can be evaluated using long-term video monitoring techniquesunder controlled conditions in laboratory aquaria. The bivalvesAnodonta cygnea and Margaritifera falcata were used to evaluatethe effect of temperature on rhythms in gape and the formationof siphons at the mantle edge. Frequency and duration of shellclosure vary with temperature in both species, but with differentresponses. Mean duration of intervals of valve closure decreasesas temperature rises in both species, and is consistent withphysiological limitation by increased biological oxygen demand.For A. cygnea, cumulative gape duration peaks at 25°C, withless time spent closed than at any other temperature, but increasingtemperatures correspond to an increase in gape frequency witha strong increase observed at 31°C. In contrast, frequencyof adduction and valve closure peak at 25°C in M. falcata,and continuous gaping is observed above 29.5°C. This physiologicalstress is consistent with evidence from sclerochronologically-calibratedstable isotope studies of shells, where growth breaks in manymarine taxa coincide with maximum temperatures above 31°Cas derived for ¹⁸O_carbonate. The results of this study suggestthat these growth breaks may be due to physiological limitationsin oxygen uptake and metabolic activity, rather than being adirect consequence of elevated temperature alone. (Received 17 March 2008; accepted 3 October 2008)     

Kinetics of lithium efflux through the (Na,K)-pump of human erythrocytes

Evidence from the kinetics of transport supports the hypothesis that cellular Li, Li_c, interacts with the internal aspect of the (Na,K)-pump as a congener of Na, Li_c and Na_c compete for the same sites on the internal aspect of the pump. Li_c promotes Na-activated K influx and Na_c promotes Li-activated K influx. Cellular K inhibits Li-activated K influx, indicating that the interaction of K_c with the internal aspect of the pump is qualitatively different from the interaction with either Na_c or Li_c. The Hill coefficients for Na-promoted and Li-promoted K influx are similar and are both greater than unity, indicating the same number of multiple intracellular sites per pump for the two cations. The stoichiometry of coupling between efflux and K influx is also similar for Na and Li, and is close to 3 Na or 3 Li to 2 K. The Li-activated K influx appears to be independent of the residual Na which remains in cells prepared in Na-free solutions.