HT-29 human colon cancer cell proliferation is regulated by cytosolic phospholipase A(2)α dependent PGE(2)via both PKA and PKB pathways

Cytosolic phospholipase A(2)α (cPLA(2)α) up-regulation has been reported in human colorectal cancer cells, thus we aimed to elucidate its role in the proliferation of the human colorectal cancer cell line, HT-29. EGF caused a rapid activation of cPLA(2)α which coincided with a significant increase in cell proliferation. The inhibition of cPLA(2)α activity by pyrrophenone or by antisense oligonucleotide against cPLA(2)α (AS) or inhibition of prostaglandin E(2) (PGE(2)) production by indomethacin resulted with inhibition of cell proliferation, that was restored by addition of PGE(2). The secreted PGE(2) activated both protein kinase A (PKA) and PKB/Akt pathways via the EP2 and EP4 receptors. Either, the PKA inhibitor (H-89) or the PKB/Akt inhibitor (Ly294002) caused a partial inhibition of cell proliferation which was restored by PGE(2). But, inhibited proliferation in the presence of both inhibitors could not be restored by addition of PGE(2). AS or H-89, but not Ly294002, inhibited CREB activation, suggesting that CREB activation is mediated by PKA. AS or Ly294002, but not H-89, decreased PKB/Akt activation as well as the nuclear localization of β-catenin and cyclin D1 and increased the plasma membrane localization of β-catenin with E-cadherin, suggesting that these processes are regulated by the PKB pathway. Similarly, Caco-2 cells exhibited cPLA(2)α dependent proliferation via activation of both PKA and PKB/Akt pathways. In conclusion, our findings suggest that the regulation of HT-29 proliferation is mediated by cPLA(2)α-dependent PGE(2) production. PGE(2)via EP induces CREB phosphorylation by the PKA pathway and regulates β-catenin and cyclin D1 cellular localization by PKB/Akt pathway.     

Linear forms of plasmid DNA are superior to supercoiled structures as active templates for gene expression in plant protoplasts

Introduction of the plasmids pUC8CaMVCAT and pNOSCAT into plant protoplasts is known to result in transient expression of the chloramphenicol acetyl transferase (CAT) gene. Also, transfection with the plasmid pDO432 results in transient appearance of the luciferase enzyme. In the present work we have used these systems to study the effect of DNA topology on the expression of the above recombinant genes. Linear forms of the above plasmids exhibited much higher activity in supporting gene expression than their corresponding super-coiled structures. CAT activity in protoplasts transfected with the linear forms of pUC8CaMVCAT and pNOSCAT was up to ten-fold higher than that observed in protoplasts transfected by the supercoiled template of these plasmids. This effect was observed in protoplasts derived from two different lines of Petunia hybrida and from a Nicotiana tabacum cell line. Transfection with the relaxed form of pUC8CaMVCAT resulted in very low expression of the CAT gene.Northern blot analysis revealed that the amount of poly(A)⁺ RNA extracted from protoplasts transformed with the linear forms of the DNA was about 10-fold higher than that found in protoplasts transformed with supercoiled DNA.Southern blot analysis revealed that about the same amounts of supercoiled and linear DNA molecules were present in nuclei of transfected protoplasts. No significant quantitative differences have been observed between the degradation rates of the various DNA templates used.     

Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis

The major cystic fibrosis (CF) mutation, F508, is associated with one haplotype (B) determined by the two polymorphic markers, XV2C and KM19. This haplotype is rare (15%) among non-F chromosomes. Its frequency among non-F508 CF chromosomes is 50% with variation between populations. One hypothesis for the high frequency of CF haplotype B chromosomes suggests that there was a selective advantage for CF mutations on this specific background as a result of epistatic selection at other closely linked loci. Since the XV2C and KM19 markers are located 200kb 5 to the CF gene and span only 60 kb, an extended haplotype analysis was needed to test this hypothesis. Haplotypes were determined for 183 CF and 120 non-CF Israeli chromosomes at the XV2C and KM19 loci and at three intragenic polymorphic sites (GATT in intron 6A, TUB18 in intron 19, and 24M in exon 24). Among the studied chromosomes the frequency of non-F508 CF chromosomes associated with haplotype B was 70% (88% among Ashkenazi CF chromosomes). Nine mutations (F508, W1282X, G542X, N1303K, 3849+10 kb CT, Q359K/T360K, S549I, S549R, and 1717-1GA) were identified among the studied chromosomes. These mutations accounted for 96% of CF chromosomes of Ashkenazi origin. Haplotype B was associated with seven of these (F508, W1282X, G542X, N1303K, Q359K/ T360K, S549R, and 1717-1GA). The extended haplotype analysis revealed that in five of the seven mutations associated with the haplotype B, 97% of the chromosomes shared the same intragenic haplotype, 212. The variation found in 3% of the chromosomes was only in the GATT repeat. Two mutations, W1282X and 1717-1GA, were associated with a completely different intragenic haplotype, 121. The results of this study indicate that grouping of CF chromosome by haplotype analysis spanning a small extragenic region might not be sufficient. In addition, the results of the extended haplotype analysis indicate that all the studied CF chromosomes that carry the same mutation derived from the same origin. Furthermore, the results indicate that the majority of the CF mutations are associated with the same extended haplotype, supporting the selective advantage hypothesis.     

Isolation of a new polymorphic TC maize microsatellite located on the long arm of chromosome 10

Simple sequence repeats (SSR), also called microsatellites, were previously proved to be an important class of DNA markers. The isolation, mapping and designing of primers to the flanking regions of a new maize SSR is reported. The new marker, with a core motif of (TC) 12, designated as MZETC34, was mapped to the long arm of chromosome 10.     

Phytochrome-membrane interactions as a factor in stomatal opening

Red light enhances stomatal opening in Commelina communis L. This light effect is reversed by far-red irradiation. Pretreatment with filipin, which competitively inhibits phytochrome binding to membranes, also inhibits light-enhanced opening. The pretreatment with filipin is more inhibitory if preceded by red irradiation, than after far-red irradiation. Similar results are obtained with cycloheximide and low temperature, which retard phytochrome synthesis more than its degradation. This result may indicate an enhanced release of phytochrome in the Pfr form from binding sites rather than release of phytochrome in the Pr form. This points towards the possibility that phytochrome degradation and its release from binding sites are coupled.     

The use of cultured Acer cells as a screening tool for mitotic inhibitors. I. Reference herbicides

Several commercially available mitosis inhibitors have been studied for their effects on an Acer pseudoplatanus cell suspension culture; these were colchicine, N-(1,1-dimethylpropynyl)3-chlorobenzamide, propyzamide and trifluralin. The last two compounds are known as preemergence herbicides. In the studied cultures, the concentrations necessary to arrest mitosis were between 50 and 100 M for colchicine, and between 10 and 100 M for propyzamide, N-(1,1-dimethylpropynyl)3-chlorobenzamide and trifluralin. However, protein synthesis, plastid and mitochondria division and dry weight increase occurred in the treated cells, leading to the formation of giant cells. These results suggest that mitosis inhibition is the fundamental effect of these compounds at the concentrations studied. At these concentrations, metabolic activities seem unaffected, in contrast with what was found previously in the case of chlorpropham. This phenylcarbamate inhibited mitosis in the same cells at 100 M, but also prevented protein synthesis and weight increase, probably as a result of its uncoupling properties.The effect of another compound, glyphosate, on Acer cell suspension cultures, was studied concurrently. At concentrations between 10 and 100 M, it only slightly decreased protein formation in the culture, and was unable to prevent mitosis from occurring.The formation of giant cells in Acer cell suspension cultures seems to be a good criterion to demonstrate that selective mitosis inhibition has taken place. This criterion might be used in the case of mitosis inhibitors acting on the G ₂-phase.

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Résumé Les effets de divers inhibiteurs de la division cellulaire ont été étudiés sur des suspensions cellulaires d' Acer pseudoplatanus. Ces produits sont la colchicine, le N-(1,1-diméthylpropynyl)3-chlorobenzamide, le propyzamide et la trifluraline. Les 2 derniers composés sont des herbicides de pré-levée. Les concentrations nécessaires pour bloquer la mitose dans les suspensions cellulaires se situent de 50 à 100 M pour la colchicine et de 10 à 100 M pour les 3 autres composés.Dans les cellules traitées la synthèse protéique, la multiplication des plastes et des mitochondries et l'augmentation de masse sèche ont lieu, entraînant la formation de cellules géantes. Ces résultats suggèrent que, aux concentrations étudiées, le blocage de la mitose est l'effet primaire de ces produits; les activités métaboliques des cellules, à ces concentrations, ne semble pas affecté contrairement à ce que l'on a observé précédemment avec le chlorprophame. Ce phénylcarbamate, en effet, inhibe la mitose des cellules d'Acer á 100 M mais aussi, et probablement du fait de ses propriétés découplantes, empêche la synthèse protéique et l'augmentation de masse sèche. Le glyphosate étudié parallèlement est incapable de bloquer la mitose entre 10 et 100 M; il freine légèrement la synthèse protéique.L'obtention de cellules géantes dans les suspensions cellulaires d'Acer pseudoplatanus semble un bon test pour mettre en évidence une inhibition sélective de la mitose. Ce critère pourrait être utilisé pour les composés antimitotiques agissant sur la phase G ₂.

     

Repressor and int synthesis of bacteriophage λ in the E. coli host mutant ER437

Molecular Genetics and Genomics - Analysis of λ phage infection of the host mutant ER437 by SDS polyacrylamide gel electrophoresis and autoradiography has revealed altered expression of...     

Water-soluble acetylcholine receptor from Torpedo californica. Solubilization,purification and characterization

The nicotinic acetylcholine receptor from electrogenic tissue of Torpedo californica was solubilized by tryptic digestion of membrane fragments obtained from autolysed tissue, without use of detergent. The water-soluble acetylcholine receptor was purified by affinity chromatography on a cobra-toxin-Sepharose resin. The purified receptor bound 4000–6000 pmol per mg protein of α-[¹²⁵]bungarotoxin, and toxin-binding was specifically inhibited by cholinergic ligands. Gel filtration revealed a single molecular species of Stokes radius $\text{125 ± 10}$ Å and on sucrose gradient centrifugation one major peak was observed of 20–22 S. Polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulfate and β-mercaptoethanol revealed two major polypeptides of mol. wt. 30 000 and 48 000.     

Summer heat stress alters the mRNA expression of selective-uptake and endocytotic receptors in bovine ovarian cells

Summer heat stress (HS) is a major factor in decreased reproductive performance in high-producing dairy cattle, possibly by affecting the steroidogenic capacity of ovarian follicles and ovarian follicular dynamics. In the present study, mRNA expression of cholesterol receptors was determined in bovine ovarian cells. Two endocytotic receptors (very-low-density lipoprotein receptor (VLDLr) and low-density lipoprotein receptor (LDLr)), and two selective-uptake receptors (scavenger receptor class B type 1 receptor (SRB1) and the lipoprotein-receptor-related protein 8 (LRP8)) were evaluated. Ovarian follicles in four diameter categories were evaluated from cows under non-heat stress (NHS) and HS conditions. As follicle size increased, expression of mRNA in NHS cows increased for the selective-uptake receptors, SRB1 and LRP8, and decreased (P<0.004) for the endocytotic receptors, LDLr and VLDLr. In contrast, in HS cows, mRNA expression did not significantly change (with increasing follicle diameter) for either receptor type. With increasing follicle diameter, cholesterol and fatty acid concentrations in the follicular fluid did not change in HS cows, whereas in NHS cows, cholesterol increased (P<0.008) and fatty acid decreased (P<0.0001). These changes paralleled those in the different lipoprotein fractions in the follicular fluid. In follicles from HS cows, the altered mRNA expression patterns for the endocytotic and selective-uptake receptors caused changes in the regulation of cholesterol supply at critical stages of folliculogenesis, which may play a role in the low turnover rates of ovarian follicles during the summer.