RESUMEN

Reiterative transcription is a non-canonical form of RNA synthesis by RNA polymerase in which a ribonucleotide specified by a single base in the DNA template is repetitively added to the nascent RNA transcript. We previously determined the X-ray crystal structure of the bacterial RNA polymerase engaged in reiterative transcription from the pyrG promoter, which contains eight poly-G RNA bases synthesized using three C bases in the DNA as a template and extends RNA without displacement of the promoter recognition σ factor from the core enzyme. In this study, we determined a series of transcript initiation complex structures from the pyrG promoter using soak-trigger-freeze X-ray crystallography. We also performed biochemical assays to monitor template DNA translocation during RNA synthesis from the pyrG promoter and in vitro transcription assays to determine the length of poly-G RNA from the pyrG promoter variants. Our study revealed how RNA slips on template DNA and how RNA polymerase and template DNA determine length of reiterative RNA product. Lastly, we determined a structure of a transcript initiation complex at the pyrBI promoter and proposed an alternative mechanism of RNA slippage and extension requiring the σ dissociation from the core enzyme.

Asunto(s)

Ligasas de Carbono-Nitrógeno/química , ARN Polimerasas Dirigidas por ADN/química , ARN Bacteriano/química , Transcripción Genética , Bacillus subtilis/química , Bacillus subtilis/genética , Ligasas de Carbono-Nitrógeno/genética , Cristalografía por Rayos X , ADN/química , ADN/genética , ARN Polimerasas Dirigidas por ADN/genética , Escherichia coli/genética , Regulación Bacteriana de la Expresión Génica/genética , Regiones Promotoras Genéticas/genética , ARN Bacteriano/genética , Factor sigma/química , Factor sigma/genética , Uridina Trifosfato/química , Uridina Trifosfato/genética

RESUMEN

The nucleotide receptors P2Y2 and P2Y4 are the most closely related G protein-coupled receptors (GPCRs) of the P2Y receptor (P2YR) family. Both subtypes couple to Gq proteins and are activated by the pyrimidine nucleotide UTP, but only P2Y2R is also activated by the purine nucleotide ATP. Agonists and antagonists of both receptor subtypes have potential as drugs e.g. for neurodegenerative and inflammatory diseases. So far, potent and selective, "drug-like" ligands for both receptors are scarce, but would be required for target validation and as lead structures for drug development. Structural information on the receptors is lacking since no X-ray structures or cryo-electron microscopy images are available. Thus, we performed receptor homology modeling and docking studies combined with mutagenesis experiments on both receptors to address the question how ligand binding selectivity for these closely related P2YR subtypes can be achieved. The orthosteric binding site of P2Y2R appeared to be more spacious than that of P2Y4R. Mutation of Y197 to alanine in P2Y4R resulted in a gain of ATP sensitivity. Anthraquinone-derived antagonists are likely to bind to the orthosteric or an allosteric site depending on their substitution pattern and the nature of the orthosteric binding site of the respective P2YR subtype. These insights into the architecture of P2Y2- and P2Y4Rs and their interactions with structurally diverse agonists and antagonist provide a solid basis for the future design of potent and selective ligands.

Asunto(s)

Receptores Purinérgicos P2Y2/metabolismo , Receptores Purinérgicos P2/metabolismo , Sitios de Unión/genética , Línea Celular Tumoral , Microscopía por Crioelectrón/métodos , Desarrollo de Medicamentos , Humanos , Ligandos , Modelos Moleculares , Mutagénesis/genética , Nucleótidos/química , Nucleótidos/genética , Receptores Acoplados a Proteínas G/genética , Receptores Acoplados a Proteínas G/metabolismo , Receptores Purinérgicos P2/genética , Receptores Purinérgicos P2/fisiología , Receptores Purinérgicos P2Y2/genética , Receptores Purinérgicos P2Y2/fisiología , Transducción de Señal/genética , Relación Estructura-Actividad , Uridina Trifosfato/química , Uridina Trifosfato/genética

RESUMEN

To determine the step-by-step kinetics and mechanism of transcription initiation and escape by E. coli RNA polymerase from the λPR promoter, we quantify the accumulation and decay of transient short RNA intermediates on the pathway to promoter escape and full-length (FL) RNA synthesis over a wide range of NTP concentrations by rapid-quench mixing and phosphorimager analysis of gel separations. Experiments are performed at 19 °C, where almost all short RNAs detected are intermediates in FL-RNA synthesis by productive complexes or end-products in nonproductive (stalled) initiation complexes and not from abortive initiation. Analysis of productive-initiation kinetic data yields composite second-order rate constants for all steps of NTP binding and hybrid extension up to the escape point (11-mer). The largest of these rate constants is for incorporation of UTP into the dinucleotide pppApU in a step which does not involve DNA opening or translocation. Subsequent steps, each of which begins with reversible translocation and DNA opening, are slower with rate constants that vary more than 10-fold, interpreted as effects of translocation stress on the translocation equilibrium constant. Rate constants for synthesis of 4- and 5-mer, 7-mer to 9-mer, and 11-mer are particularly small, indicating that RNAP-promoter interactions are disrupted in these steps. These reductions in rate constants are consistent with the previously determined ∼9 kcal cost of escape from λPR. Structural modeling and previous results indicate that the three groups of small rate constants correspond to sequential disruption of in-cleft, -10, and -35 interactions. Parallels to escape by T7 RNAP are discussed.

Asunto(s)

ARN Polimerasas Dirigidas por ADN/metabolismo , Proteínas de Escherichia coli/metabolismo , Regiones Promotoras Genéticas/genética , Iniciación de la Transcripción Genética , Algoritmos , Escherichia coli/genética , Escherichia coli/metabolismo , Cinética , Modelos Genéticos , Nucleótidos/genética , Nucleótidos/metabolismo , Oligorribonucleótidos/genética , Oligorribonucleótidos/metabolismo , ARN Bacteriano/genética , ARN Bacteriano/metabolismo , Uridina Trifosfato/genética , Uridina Trifosfato/metabolismo

RESUMEN

Eukaryotic ribosome biogenesis is a multistep process involving more than 150 biogenesis factors, which interact transiently with pre-ribosomal particles to promote their maturation. Some of these auxiliary proteins have been isolated in complexes found separate from the ribosomal environment. Among them, are 3 large UTP subcomplexes containing 6 or 7 protein subunits which are involved in the early steps of ribosome biogenesis. The composition of the UTP subcomplexes and the network of binary interactions between protein subunits have been analyzed previously. To obtain further insights into the structural and biochemical properties of UTP subcomplexes, we established a heterologous expression system to allow reconstitution of the yeast tUTP/UTP A and UTP B subcomplexes from their candidate subunits. The results of a series of reconstitution experiments involving different combinations of protein subunits are in good agreement with most of the previously observed binary interactions. Moreover, in combination with additional biochemical analyses, several stable building blocks of the UTP subcomplexes were identified. Based on these findings, we present a refined model of the tUTP/UTP A and UTP B architecture.

Asunto(s)

Complejos Multiproteicos/metabolismo , Biogénesis de Organelos , Ribonucleoproteínas/metabolismo , Ribosomas/metabolismo , Proteínas de Saccharomyces cerevisiae/metabolismo , Uridina Trifosfato/metabolismo , Levaduras/citología , Animales , Western Blotting , Células Cultivadas , Técnicas In Vitro , Insectos , Complejos Multiproteicos/genética , Oligonucleótidos , Ribonucleoproteínas/genética , Proteínas de Saccharomyces cerevisiae/genética , Espectrometría de Masas en Tándem , Uridina Trifosfato/genética , Levaduras/metabolismo

RESUMEN

The voltage-dependent anion channel (VDAC) mediates and gates the flux of metabolites and ions across the outer mitochondrial membrane and is a key player in cellular metabolism and apoptosis. Here we characterized the binding of nucleotides to human VDAC1 (hVDAC1) on a single-residue level using NMR spectroscopy and site-directed mutagenesis. We find that hVDAC1 possesses one major binding region for ATP, UTP, and GTP that partially overlaps with a previously determined NADH binding site. This nucleotide binding region is formed by the N-terminal α-helix, the linker connecting the helix to the first ß-strand and adjacent barrel residues. hVDAC1 preferentially binds the charged forms of ATP, providing support for a mechanism of metabolite transport in which direct binding to the charged form exerts selectivity while at the same time permeation of the Mg(2+)-complexed ATP form is possible.

Asunto(s)

Adenosina Trifosfato/química , Guanosina Trifosfato/química , NAD/química , Uridina Trifosfato/química , Canal Aniónico 1 Dependiente del Voltaje/química , Adenosina Trifosfato/genética , Adenosina Trifosfato/metabolismo , Transporte Biológico Activo/fisiología , Guanosina Trifosfato/genética , Guanosina Trifosfato/metabolismo , Humanos , NAD/genética , NAD/metabolismo , Unión Proteica , Estructura Secundaria de Proteína , Uridina Trifosfato/genética , Uridina Trifosfato/metabolismo , Canal Aniónico 1 Dependiente del Voltaje/genética , Canal Aniónico 1 Dependiente del Voltaje/metabolismo

RESUMEN

Nephrolithiasis remains a major health problem in Western countries. Seventy to 80% of kidney stones are composed of calcium oxalate, and small changes in urinary oxalate affect risk of kidney stone formation. Intestinal oxalate secretion mediated by the anion exchanger SLC26A6 plays an essential role in preventing hyperoxaluria and calcium oxalate nephrolithiasis, indicating that understanding the mechanisms regulating intestinal oxalate transport is critical for management of hyperoxaluria. Purinergic signaling modulates several intestinal processes through pathways including PKC activation, which we previously found to inhibit Slc26a6 activity in mouse duodenal tissue. We therefore examined whether purinergic stimulation with ATP and UTP affects oxalate transport by human intestinal Caco-2-BBe (C2) cells. We measured [¹4C]oxalate uptake in the presence of an outward Cl⁻ gradient as an assay of Cl⁻/oxalate exchange activity, ≥50% of which is mediated by SLC26A6. We found that ATP and UTP significantly inhibited oxalate transport by C2 cells, an effect blocked by the PKC inhibitor Gö-6983. Utilizing pharmacological agonists and antagonists, as well as PKC-δ knockdown studies, we observed that ATP inhibits oxalate transport through the P2Y2 receptor, PLC, and PKC-δ. Biotinylation studies showed that ATP inhibits oxalate transport by lowering SLC26A6 surface expression. These findings are of potential relevance to pathophysiology of inflammatory bowel disease-associated hyperoxaluria, where supraphysiological levels of ATP/UTP are expected and overexpression of the P2Y2 receptor has been reported. We conclude that ATP and UTP inhibit oxalate transport by lowering SLC26A6 surface expression in C2 cells through signaling pathways including the P2Y2 purinergic receptor, PLC, and PKC-δ.

Asunto(s)

Oxalatos/metabolismo , Proteína Quinasa C-delta/metabolismo , Adenosina Trifosfato/genética , Adenosina Trifosfato/metabolismo , Animales , Transporte Biológico/efectos de los fármacos , Transporte Biológico/fisiología , Células CACO-2 , Activación Enzimática , Técnicas de Silenciamiento del Gen , Humanos , Proteínas de Transporte de Membrana/genética , Proteínas de Transporte de Membrana/metabolismo , Ratones , Proteína Quinasa C-delta/genética , Receptores Purinérgicos P2Y2/genética , Receptores Purinérgicos P2Y2/metabolismo , Transportadores de Sulfato , Uridina Trifosfato/genética , Uridina Trifosfato/metabolismo

RESUMEN

Uridine, adenosine, guanosine, and cytidine that carry a propargyl group attached to the 2'-oxygen were converted efficiently to the corresponding nucleoside triphosphates (pNTPs). Primer extension experiments revealed that pUTP, pATP, and pGTP can be successfully incorporated in oligonucleotides in the so-called 9°N and Therminator DNA polymerases. Most importantly, the ethynyl group as single 2'-modification of the enzymatically prepared oligonucleotides can be applied for postsynthetic labeling. This was representatively shown by PAGE analysis after the "click"-type cycloaddition with the fluorescent nile red azide. These results show that the 2'-position as one of the most important modification sites in oligonucleotides is now accessible not only for synthetic, but also for enzymatic oligonucleotide preparation.

Asunto(s)

Adenosina Trifosfato/síntesis química , Química Clic/métodos , ADN/síntesis química , Guanosina Trifosfato/síntesis química , Oxazinas/síntesis química , Uridina Trifosfato/síntesis química , Adenosina Trifosfato/genética , ADN/genética , Colorantes Fluorescentes/síntesis química , Guanosina Trifosfato/genética , Oligonucleótidos/síntesis química , Oligonucleótidos/genética , Uridina Trifosfato/genética

RESUMEN

Hepatitis C virus (HCV) RNA-dependent RNA polymerase replicates the viral genomic RNA and is a primary drug target for antiviral therapy. Previously, we described the purification of an active and stable polymerase-primer-template elongation complex. Here, we show that, unexpectedly, the polymerase elongation complex can use NTPs to excise the terminal nucleotide in nascent RNA. Mismatched ATP, UTP, or CTP could mediate excision of 3'-terminal CMP to generate the dinucleoside tetraphosphate products Ap(4)C, Up(4)C, and Cp(4)C, respectively. Pre-steady-state kinetic studies showed that the efficiency of NTP-mediated excision was highest with ATP. A chain-terminating inhibitor, 3'deoxy-CMP, could also be excised through this mechanism, suggesting important implications for nucleoside drug potency and resistance. The nucleotide excision reaction catalyzed by recombinant hepatitis C virus polymerase was 100-fold more efficient than the corresponding reaction observed with HIV reverse transcriptase.

Asunto(s)

Hepacivirus/metabolismo , Nucleótidos/metabolismo , ARN Polimerasa Dependiente del ARN/metabolismo , Proteínas no Estructurales Virales/metabolismo , Adenosina Trifosfato/química , Adenosina Trifosfato/genética , Adenosina Trifosfato/metabolismo , Secuencia de Bases , Citidina Monofosfato/química , Citidina Monofosfato/metabolismo , Citidina Trifosfato/química , Citidina Trifosfato/genética , Citidina Trifosfato/metabolismo , Fosfatos de Dinucleósidos/química , Fosfatos de Dinucleósidos/metabolismo , Transcriptasa Inversa del VIH/metabolismo , Hepacivirus/enzimología , Hepacivirus/genética , Cinética , Modelos Químicos , Modelos Genéticos , Nucleótidos/química , Nucleótidos/genética , ARN Viral/genética , ARN Viral/metabolismo , Uridina Trifosfato/química , Uridina Trifosfato/genética , Uridina Trifosfato/metabolismo

RESUMEN

The causative agent of African sleeping sickness, Trypanosoma brucei , undergoes an unusual mitochondrial RNA editing process that is essential for its survival. RNA editing terminal uridylyl transferase 2 of T. brucei (TbRET2) is an indispensable component of the editosome machinery that performs this editing. TbRET2 is required to maintain the vitality of both the insect and bloodstream forms of the parasite, and with its high-resolution crystal structure, it poses as a promising pharmaceutical target. Neither the exclusive requirement of uridine 5'-triphosphate (UTP) for catalysis, nor the RNA primer preference of TbRET2 is well-understood. Using all-atom explicitly solvated molecular dynamics (MD) simulations, we investigated the effect of UTP binding on TbRET2 structure and dynamics, as well as the determinants governing TbRET2's exclusive UTP preference. Through our investigations of various nucleoside triphosphate substrates (NTPs), we show that UTP preorganizes the binding site through an extensive water-mediated H-bonding network, bringing Glu424 and Arg144 side chains to an optimum position for RNA primer binding. In contrast, cytosine 5'-triphosphate (CTP) and adenosine 5'-triphosphate (ATP) cannot achieve this preorganization and thus preclude productive RNA primer binding. Additionally, we have located ligand-binding "hot spots" of TbRET2 based on the MD conformational ensembles and computational fragment mapping. TbRET2 reveals different binding pockets in the apo and UTP-bound MD simulations, which could be targeted for inhibitor design.

Asunto(s)

Nucleótidos , Edición de ARN , ARN Nucleotidiltransferasas/genética , ARN Nucleotidiltransferasas/metabolismo , Trypanosoma brucei brucei/enzimología , Sitios de Unión , Modelos Moleculares , Simulación de Dinámica Molecular , Nucleótidos/genética , Especificidad por Sustrato , Uridina Trifosfato/genética , Uridina Trifosfato/metabolismo , Agua/química

RESUMEN

The Leishmania parasite glycocalyx is rich in galactose-containing glycoconjugates that are synthesized by specific glycosyltransferases that use UDP-galactose as a glycosyl donor. UDP-galactose biosynthesis is thought to be predominantly a de novo process involving epimerization of the abundant nucleotide sugar UDP-glucose by the UDP-glucose 4-epimerase, although galactose salvage from the environment has been demonstrated for Leishmania major. Here, we present the characterization of an L. major UDP-sugar pyrophosphorylase able to reversibly activate galactose 1-phosphate into UDP-galactose thus proving the existence of the Isselbacher salvage pathway in this parasite. The ordered bisubstrate mechanism and high affinity of the enzyme for UTP seem to favor the synthesis of nucleotide sugar rather than their pyrophosphorolysis. Although L. major UDP-sugar pyrophosphorylase preferentially activates galactose 1-phosphate and glucose 1-phosphate, the enzyme is able to act on a variety of hexose 1-phosphates as well as pentose 1-phosphates but not hexosamine 1-phosphates and hence presents a broad in vitro specificity. The newly identified enzyme exhibits a low but significant homology with UDP-glucose pyrophosphorylases and conserved in particular is the pyrophosphorylase consensus sequence and residues involved in nucleotide and phosphate binding. Saturation transfer difference NMR spectroscopy experiments confirm the importance of these moieties for substrate binding. The described leishmanial enzyme is closely related to plant UDP-sugar pyrophosphorylases and presents a similar substrate specificity suggesting their common origin.

Asunto(s)

Galactosafosfatos/metabolismo , Leishmania major/enzimología , Nucleotidiltransferasas/metabolismo , Proteínas Protozoarias/metabolismo , Uridina Difosfato/metabolismo , Secuencia de Aminoácidos , Animales , Evolución Molecular , Galactosafosfatos/genética , Glucofosfatos/genética , Glucofosfatos/metabolismo , Glicocálix/enzimología , Glicocálix/genética , Leishmania major/genética , Datos de Secuencia Molecular , Nucleotidiltransferasas/genética , Proteínas Protozoarias/genética , Especificidad por Sustrato/fisiología , Uridina Difosfato/genética , Uridina Trifosfato/genética , Uridina Trifosfato/metabolismo

RESUMEN

Respiratory syncytial virus (RSV) infection has been shown to reduce Na+-driven alveolar fluid clearance in BALB/c mice in vivo. To investigate the cellular mechanisms by which RSV inhibits amiloride-sensitive epithelial Na+ channels (ENaC), the main pathways through which Na+ ions enter lung epithelial cells, we infected human Clara-like lung (H441) cells with RSV that expresses green fluorescent protein (rRA2). 3-6 days later patch clamp recordings showed that infected cells (i.e. cells expressing green fluorescence; GFP+) had significantly lower whole-cell amiloride-sensitive currents and single channel activity (NPo) as compared with non-infected (GFP-), non-inoculated, or cells infected with UV-inactivated RSV. Both alpha and beta ENaC mRNA levels were significantly reduced in GFP+ cells as measured by real-time reverse transcription-PCR. Infection with RSV increased expression of the inducible nitric-oxide synthase (iNOS) and nitrite concentration in the culture medium; nuclear translocation of NF-kappaB p65 subunit and NF-kappaB activation were also up-regulated. iNOS up-regulation in GFP+ cells was prevented by knocking down IkappaB kinase gamma before infection. Furthermore, pretreatment of H441 cells with the specific iNOS inhibitor 1400W (1 microM) resulted in a doubling of the amiloride-sensitive Na+ current in GFP+ cells. Additionally, preincubation of H441 cells with A77-1726 (20 microM), a de novo UTP synthesis inhibitor, and 1400W completely reversed the RSV inhibition of amiloride-sensitive currents in GFP+ cells. Thus, both UTP- and iNOS-generated reactive species contribute to ENaC down-regulation in RSV-infected airway epithelial cells.

Asunto(s)

Células Epiteliales/metabolismo , Canales Epiteliales de Sodio/biosíntesis , Óxido Nítrico Sintasa de Tipo II/metabolismo , Mucosa Respiratoria/metabolismo , Infecciones por Virus Sincitial Respiratorio/metabolismo , Virus Sincitiales Respiratorios/metabolismo , Uridina Trifosfato/metabolismo , Compuestos de Anilina/farmacología , Animales , Antiinflamatorios no Esteroideos/farmacología , Línea Celular , Crotonatos , Regulación hacia Abajo/efectos de los fármacos , Regulación hacia Abajo/genética , Células Epiteliales/virología , Canales Epiteliales de Sodio/genética , Técnicas de Silenciamiento del Gen , Humanos , Hidroxibutiratos/farmacología , Quinasa I-kappa B/genética , Quinasa I-kappa B/metabolismo , Pulmón , Ratones , Ratones Endogámicos BALB C , Óxido Nítrico Sintasa de Tipo II/genética , Nitrilos , Nitritos/metabolismo , Mucosa Respiratoria/virología , Infecciones por Virus Sincitial Respiratorio/genética , Virus Sincitiales Respiratorios/genética , Sodio , Toluidinas , Factor de Transcripción ReIA/genética , Factor de Transcripción ReIA/metabolismo , Regulación hacia Arriba/efectos de los fármacos , Regulación hacia Arriba/genética , Uridina Trifosfato/genética

RESUMEN

Terminal RNA uridylyltransferases (TUTases) are functionally and structurally diverse nucleotidyl transferases that catalyze template-independent 3' uridylylation of RNAs. Within the DNA polymerase beta-type superfamily, TUTases are closely related to non-canonical poly(A) polymerases. Studies of U-insertion/deletion RNA editing in mitochondria of trypanosomatids identified the first TUTase proteins and their cellular functions: post-transcriptional uridylylation of guide RNAs by RNA editing TUTase 1 (RET1) and U-insertion mRNA editing by RNA editing TUTase 2 (RET2). The editing TUTases possess conserved catalytic and nucleotide base recognition domains, yet differ in quaternary structure, substrate specificity and processivity. The cytosolic TUTases TUT3 and TUT4 have also been identified in trypanosomes but their biological roles remain to be established. Structural analyses have revealed a mechanism of cognate nucleoside triphosphate selection by TUTases, which includes protein-UTP contacts as well as contribution of the RNA substrate. This review focuses on biological functions and structures of trypanosomal TUTases.

Asunto(s)

Poli U/metabolismo , Polirribonucleótido Nucleotidiltransferasa/metabolismo , Proteínas Protozoarias/metabolismo , Edición de ARN/fisiología , ARN Protozoario/metabolismo , Trypanosoma/enzimología , Animales , Mitocondrias/genética , Mitocondrias/metabolismo , Proteínas Mitocondriales/genética , Proteínas Mitocondriales/metabolismo , Poli U/genética , Polirribonucleótido Nucleotidiltransferasa/genética , Estructura Terciaria de Proteína/fisiología , Proteínas Protozoarias/genética , ARN/genética , ARN/metabolismo , ARN Mitocondrial , ARN Protozoario/genética , Relación Estructura-Actividad , Especificidad por Sustrato/fisiología , Trypanosoma/genética , Uridina Trifosfato/genética , Uridina Trifosfato/metabolismo

RESUMEN

Seven UTP derivatives modified at the 5-position through an amide linkage were tested as substrates for T7 RNA polymerase (T7 RNAP) transcription. All UTP derivatives gave good yields of full-length transcript even from DNA templates that showed a significant number of abortive transcripts using unmodified UTP. A kinetic assay to determine the relative K(m) and V(max) for T7 RNAP transcription gave surprisingly similar values for UTP and the 5-position hydrophobic modifications phenyl, 4-pyridyl, 2-pyridyl, indolyl, and isobutyl. The 5-position modifications imidazole and amino, which could both be positively charged, gave K(m) values significantly higher than UTP. All seven UTP derivatives gave relative V(max) values similar to UTP, indicating that insertion of these modified bases into the transcript did not impede its elongation.

Asunto(s)

ARN Polimerasas Dirigidas por ADN/metabolismo , Transcripción Genética/fisiología , Uridina Trifosfato/análogos & derivados , Bacteriófago T7/enzimología , Secuencia de Bases , ADN/genética , ADN/metabolismo , Cinética , Datos de Secuencia Molecular , ARN/genética , ARN/metabolismo , Especificidad por Sustrato , Uridina Trifosfato/genética , Uridina Trifosfato/metabolismo , Proteínas Virales

RESUMEN

The 5'-triphosphates of 2'-hydroxymethyluridine (2'-homouridine) and 2'-hydroxyethyluridine were prepared from the corresponding acetyl-protected nucleosides by initial phosphitylation with 2-chloro-5,6-benzo-1,2,3-dioxaphosphorin-4-one. 2'-Acetamidouridine 5'-triphosphate was prepared in an analogous fashion from uridine 2'-C-, 3'-O-gamma-butyrolactone, in which the 3'-hydroxyl group is internally protected as the lactone. Subsequent treatment with ammonia gave the required acetamido triphosphate. All three triphosphates were investigated as substrates for T7 RNA polymerase and a Y639F mutant of this enzyme. 2'-Homouridine triphosphate was found to be a substrate for the wild-type enzyme in the presence of manganese and was specifically incorporated into short RNA transcripts (20 and 21 nucleotides in length). The presence of the analogue within the transcripts was confirmed through its resistance to alkaline hydrolysis. Gel electrophoretic analysis also showed that 2'-homouridine could be multiply incorporated into a transcript with a length of 75 nucleotides. This is the first report of a 2'-deoxy-2'-alpha-C-branched nucleoside 5'-triphosphate acting as a substrate for T7 RNA polymerase. The 2'-hydroxyethyl- and 2'-acetamido -uridine triphosphates were not substrates for the enzymes.

Asunto(s)

ARN Polimerasas Dirigidas por ADN/metabolismo , Transcripción Genética , Uridina Trifosfato/síntesis química , Uridina/química , Proteínas Virales/metabolismo , ARN Polimerasas Dirigidas por ADN/genética , Electroforesis en Gel de Poliacrilamida , Mutación , Uridina Trifosfato/análogos & derivados , Uridina Trifosfato/genética , Proteínas Virales/genética

RESUMEN

5-Aminoallyl-2'-fluoro-dUTP, 5-aminoallyl-UTP, and N(6)-([6-aminohexyl]carbamoylmethyl)-ATP were systematically tested for their suitability for the systematic evolution of ligands by exponential enrichment (SELEX) process with the aim of introducing additional functionalities to RNA libraries. All three aminomodified nucleoside triphosphates proved to be compatible with the enzymatic steps required for SELEX and maintained strict Watson-Crick basepairing. Complementary RNA molecules modified with the two uridine analogues show a significantly increased melting temperature, whereas the introduction of N(6)-([6-aminohexyl]carbamoylmethyl)-ATP leads to a decreased T(m) and thus less stable basepairing. The chemical synthesis of 5-aminoallyl-2'-fluoro-dUTP is reported in detail.

Asunto(s)

Adenosina Trifosfato/química , Análisis de Secuencia de ARN/métodos , Uridina Trifosfato/química , Adenosina Trifosfato/genética , Animales , Secuencia de Bases , Bovinos , Venenos de Crotálidos , Crotalus , Biblioteca de Genes , ARN/análisis , ARN/química , ARN/genética , Uridina Trifosfato/genética

RESUMEN

Microarrays of oligonucleotide expression libraries can be hybridised with either cDNA, generated from mRNA during reverse transcription, or cRNA, generated in an Eberwine mRNA amplification procedure. While methods for fluorescent labelling of cDNA have been thoroughly investigated, methods for cRNA labelling have not. To this purpose, we developed an aminoallyl-UTP (aa-UTP) driven cRNA labelling protocol and compared it in expression profiling studies using spotted 7.5 K 65mer murine oligonucleotide arrays with labelling via direct incorporation of Cy-UTPs. The presence of dimethylsulfoxide during coupling of aa-modified cRNA with N-hydroxysuccinimide-modified, fluorescent Cy dyes greatly enhanced the labelling efficiency, as analysed by spectrophotometry and fluorescent hybridisation signals. Indirect labelling using aa-UTP resulted in 2- to 3-fold higher degrees of labelling and fluorescent signals than labelling by direct incorporation of Cy-UTP. By variation of the aa-UTP:UTP ratio, a clear optimal degree of labelling was found (1 dye per 20-25 nt). Incorporation of more label increased Cy3 signal but lowered Cy5 fluorescence. This effect is probably due to quenching, which is more prominent for Cy5 than for Cy3. In conclusion, the currently developed method is an efficient, robust and inexpensive technique for fluorescent labelling of cRNA and allows sensitive detection of gene expression profiles on oligonucleotide microarrays.

Asunto(s)

Colorantes Fluorescentes/química , Análisis de Secuencia por Matrices de Oligonucleótidos/métodos , ARN Complementario/genética , Carbocianinas/química , ARN Complementario/química , Espectrofotometría , Uridina Trifosfato/química , Uridina Trifosfato/genética

RESUMEN

We find that immediately following transcript initiation, RNA polymerase II pauses at several locations even in the presence of relatively high (200 microM) levels of nucleoside triphosphates. Strong pauses with half-lives of >30 s were observed at +7, +18/19, and about +25 on the template used in these experiments. We show that the strong pause at +7, after the synthesis of 5'-ACUCUCU, leads to repeated cycles of upstream slippage of the RNA-DNA hybrid followed by re-pairing with the DNA and continued RNA synthesis. The resulting transcripts are 2, 4, and 6 bases longer than predicted by the template sequence. Slippage is efficient when transcription is primed with the +1/+2 (ApC) dinucleotide, and it occurs at even higher levels with the +2/+3 primer (CpU). Slippage can occur at high levels with ATP initiation, but priming with CpA (-1/+1) supports very little slippage. This latter result is not simply an effect of transcript length at the point of pausing. Slippage can also occur with a second template on which the polymerase can be paused after synthesizing ACUCU. Slippage is not reduced by an ATP analog that blocks promoter escape, but it is inhibited by substitution of 5Br-U for U in the RNA. Our results reveal an unexpected flexibility of RNA polymerase II ternary complexes during the very early stage of transcription, and they suggest that initiation at different locations within the same promoter gives rise to transcription complexes with different properties.

Asunto(s)

ARN Polimerasa II/metabolismo , ARN/biosíntesis , Transcripción Genética/fisiología , Adenosina Trifosfato/análogos & derivados , Adenosina Trifosfato/genética , Adenosina Trifosfato/metabolismo , Citidina Trifosfato/genética , Citidina Trifosfato/metabolismo , Guanosina Trifosfato/genética , Guanosina Trifosfato/metabolismo , Células HeLa , Humanos , Regiones Promotoras Genéticas , Sitio de Iniciación de la Transcripción , Uridina Trifosfato/análogos & derivados , Uridina Trifosfato/genética , Uridina Trifosfato/metabolismo

RESUMEN

Efficient transcription termination downstream of poly(A) sites has been shown to correlate with the strength of an upstream polyadenylation signal and the presence of a polymerase pause site. To further investigate the mechanism linking termination with 3'-end processing, we analyzed the cis-acting elements that contribute to these events in the Saccharomyces cerevisiae FBP1 gene. FBP1 has a complex polyadenylation signal, and at least three efficiency elements must be present for efficient processing. However, not all combinations of these elements are equally effective. This gene also shows a novel organization of sequence elements. A strong positioning element is located upstream, rather than downstream, of the efficiency elements, and functions to select the cleavage site in vitro and in vivo. Transcription run-on analysis indicated that termination occurs within 61 nt past the poly(A) site. Deletion of two UAUAUA-type efficiency elements greatly reduces polyadenylation in vivo and in vitro, but transcription termination is still efficient, implying that FBP1 termination signals may be distinct from those for polyadenylation. Alternatively, assembly of a partial, but nonfunctional, polyadenylation complex on the nascent transcript may be sufficient to cause termination.

Asunto(s)

Proteínas Fúngicas/genética , Genes Fúngicos/genética , Poli A/genética , Procesamiento Postranscripcional del ARN , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/genética , Transcripción Genética , Secuencia de Bases , Repeticiones de Dinucleótido , Fructosa-Bifosfatasa , Datos de Secuencia Molecular , Radioisótopos de Fósforo , ARN Polimerasa II/genética , ARN Polimerasa II/metabolismo , Precursores del ARN , ARN Mensajero/genética , Eliminación de Secuencia , Uridina Trifosfato/genética , Uridina Trifosfato/metabolismo

RESUMEN

In vitro DNA-dependent RNA transcription using bacteriophage T3 RNA polymerase may be rendered hypermutagenic by employing biased nucleoside triphosphate (NTP) concentrations and manganese cations. Using the E. coli R67 plasmid-encoded dihydrofolate reductase (DHFR) gene as target substitution rates approaching 4 x 10(-2) per base per reaction could be achieved, on a par with hypermutagenic reverse transcription. In all cases the majority of substitutions was that expected from the NTP pool bias. The addition of manganese ions increased the frequency of mutations, particularly the proportion of transversions. Functional DHFR hypermutants with up to 8% amino acid substitutions were readily obtained from a single reaction which, given the unique mutation matrix allows exploration of sequence space complementary to that accessed by other hypermutagenic protocols.

Asunto(s)

Manganeso/química , Mutagénesis , Nucleósidos/genética , Tetrahidrofolato Deshidrogenasa/genética , Transcripción Genética , Adenosina Trifosfato/genética , Secuencia de Aminoácidos , Ampicilina/farmacología , Cationes/química , Citidina Trifosfato/genética , ARN Polimerasas Dirigidas por ADN/genética , ARN Polimerasas Dirigidas por ADN/metabolismo , Guanosina Trifosfato/genética , Datos de Secuencia Molecular , Mutación , Tetrahidrofolato Deshidrogenasa/efectos de los fármacos , Tetrahidrofolato Deshidrogenasa/metabolismo , Trimetoprim/farmacología , Uridina Trifosfato/genética

RESUMEN

Excitotoxic lesion of the medial septum with ibotenic acid leading to partial disappearance of the septal cholinergic nerve cells was used to investigate the role of cholinergic mechanisms in the control of trophic factors for hippocampal plasticity, namely brain-derived neurotrophic factor (BDNF) and glucocorticoid receptor (GR). Their mRNA levels were tested by in situ hybridization 13 days after the lesion. A persistent and widespread increase of BDNF mRNA was found in all parts of the dorsal hippocampal formation that was not accompanied by a significant modification in GR expression. The present data suggest that subcortical excitotoxic lesions at the septal level have long-term consequences for the adaptive trophic responses occurring in the dorsal hippocampus.

Asunto(s)

Factor Neurotrófico Derivado del Encéfalo/genética , Agonistas de Aminoácidos Excitadores/farmacología , Hipocampo/efectos de los fármacos , Ácido Iboténico/farmacología , Núcleos Septales/efectos de los fármacos , Animales , Supervivencia Celular/efectos de los fármacos , Colina O-Acetiltransferasa/metabolismo , Fibras Colinérgicas/efectos de los fármacos , Hipocampo/citología , Hipocampo/enzimología , Hibridación in Situ , Masculino , Microinyecciones , Neurotoxinas/farmacología , Sondas ARN , ARN Mensajero/metabolismo , Ratas , Ratas Sprague-Dawley , Núcleos Septales/citología , Núcleos Septales/fisiología , Radioisótopos de Azufre , Uridina Trifosfato/genética