94 documentos corresponden a la consulta.
Palabras contadas: rna: 350
Filomatori, C.V. - Lodeiro, M.F. - Alvarez, D.E. - Samsa, M.M. - Pietrasanta, L. - Gamarnik, A.V.
Genes Dev. 2006;20(16):2238-2249
2006
Temas: AFM - Flavivirus - RNA cyclization - RNA-dependent RNA polymerase - Viral RNA synthesis - article - controlled study - Dengue virus - genome - nonhuman
Descripción: The mechanisms of RNA replication of plus-strand RNA viruses are still unclear. Here, we identified the first promoter element for RNA synthesis described in a flavivirus. Using dengue virus as a model, we found that the viral RdRp discriminates the viral RNA by specific recognition of a 5′ element named SLA. We demonstrated that RNA-RNA interactions between 5′ and 3′ end sequences of the viral genome enhance dengue virus RNA synthesis only in the presence of an intact SLA. We propose a novel mechanism for minus-strand RNA synthesis in which the viral polymerase binds SLA at the 5′ end of the genome and reaches the site of initiation at the 3′ end via long-range RNA-RNA interactions. These findings provide an explanation for the strict requirement of dengue virus genome cyclization during viral replication. © 2006 by Cold Spring Harbor Laboratory Press.
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Caceres, J.F. - Krainer, A.R. - Kornblihtt, A.R.
EMBO Rep. 2007;8(8):730-734
2007
Temas: arginine - messenger RNA - protein - serine - transcription factor - alternative RNA splicing - cancer - conference paper - gene expression - gene mutation
Descripción: Fil:Caceres, J.F. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
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Alvarez, D.E. - Lodeiro, M.F. - Ludueña, S.J. - Pietrasanta, L.I. - Gamarnik, A.V.
J. Virol. 2005;79(11):6631-6643
2005
Temas: virus RNA - article - atomic force microscopy - base pairing - binding assay - cyclization - Dengue virus - Flavivirus - genetic transfection - immunofluorescence
Descripción: Secondary and tertiary RNA structures present in viral RNA genomes play essential regulatory roles during translation, RNA replication, and assembly of new viral particles. In the case of flaviviruses, RNA-RNA interactions between the 5′ and 3′ ends of the genome have been proposed to be required for RNA replication. We found that two RNA elements present at the ends of the dengue virus genome interact in vitro with high affinity. Visualization of individual molecules by atomic force microscopy reveled that physical interaction between these RNA elements results in cyclization of the viral RNA. Using RNA binding assays, we found that the putative cyclization sequences, known as 5′ and 3′ CS, present in all mosquito-borne flaviviruses, were necessary but not sufficient for RNA-RNA interaction. Additional sequences present at the 5′ and 3′ untranslated regions of the viral RNA were also required for RNA-RNA complex formation. We named these sequences 5′ and 3′ UAR (upstream AUG region). In order to investigate the functional role of 5′-3′ UAR complementarity, these sequences were mutated either separately, to destroy base pairing, or simultaneously, to restore complementarity in the context of full-length dengue virus RNA. Nonviable viruses were recovered after transfection of dengue virus RNA carrying mutations either at the 5′ or 3′ UAR, while the RNA containing the compensatory mutations was able to replicate. Since sequence complementarity between the ends of the genome is required for dengue virus viability, we propose that cyclization of the RNA is a required conformation for viral replication. Copyright © 2005, American Society for Microbiology. All Rights Reserved.
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Cramer, P. - Srebrow, A. - Kadener, S. - Werbajh, S. - De La Mata, M. - Melen, G. - Nogués, G. - Kornblihtt, A.R.
FEBS Lett. 2001;498(2-3):179-182
2001
Temas: Carboxy-terminal domain - Coupling - mRNA processing - RNA polymerase II - messenger RNA - RNA polymerase II - capping phenomenon - carboxy terminal sequence - cell nucleus - nonhuman
Descripción: A large body of work has proved that transcription by RNA polymerase II and pre-mRNA processing are coordinated events within the cell nucleus. Capping, splicing and polyadenylation occur while transcription proceeds, suggesting that RNA polymerase II plays a role in the regulation of these events. The presence and degree of phosphorylation of the carboxy-terminal domain of RNA polymerase II large subunit is important for functioning of the capping enzymes, the assembly of spliceosomes and the binding of the cleavage/polyadenylation complex. Nuclear architecture and gene promoter structure have also been shown to play key roles in coupling between transcription and splicing. © 2001 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
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Baez, M.V. - Boccaccio, G.L.
J. Biol. Chem. 2005;280(52):43131-43140
2005
Temas: Degradation - Genes - Proteins - RNA - Deadenylation - Gene expression - RNA-binding proteins - Cytology - messenger RNA - protein mSmaug 1
Descripción: Cytoplasmic events depending on RNA-binding proteins contribute to the fine-tuning of gene expression. Sterile α motif-containing RNA-binding proteins constitute a novel family of post-transcriptional regulators that recognize a specific RNA sequence motif known as Smaug recognition element (SRE). The Drosophila member of this family, dSmaug, triggers the translational repression and deadenylation of maternal mRNAs by independent mechanisms, and the yeast homologue Vts1 stimulates degradation of SRE-containing messengers. Two homologous genes are present in the mammalian genome. Here we showed that hSmaug 1, encoded in human chromosome 14, represses the translation of reporter transcripts carrying SRE motifs. When expressed in fibroblasts, hSmaug 1 forms cytoplasmic granules that contain polyadenylated mRNA and the RNA-binding proteins Staufen, TIAR, TIA-1, and HuR. Smaug 1 foci are distinct from degradation foci. The murine protein mSmaug 1 is expressed in the central nervous system and is abundant in post-synaptic densities, a subcellular region where translation is tightly regulated by synaptic stimulation. Biochemical analysis indicated that mSmaug 1 is present in synaptoneurosomal 20 S particles. These results suggest a role for mammalian Smaug 1 in RNA granule formation and translation regulation in neurons. © 2005 by The American Society for Biochemistry and Molecular Biology, Inc.
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Pearson, J.L. - Robinson, T.J. - Muñoz, M.J. - Kornblihtt, A.R. - Garcia-Blanco, M.A.
J. Biol. Chem. 2008;283(12):7949-7961
2008
Temas: Binding energy - Binding sites - Biochemistry - Gene expression - Nucleic acids - Polymers - Proteins - RNA - Targets - Transcription factors
Descripción: The transcription factor TCERG1 (also known as CA150) associates with RNA polymerase II holoenzyme and alters the elongation efficiency of reporter transcripts. TCERG1 is also found as a component of highly purified spliceosomes and has been implicated in splicing. To elucidate the function of TCERG1, we used short interfering RNA-mediated knockdown followed by en masse gene expression analysis to identify its cellular targets. Analysis of data from HEK293 and HeLa cells identified high confidence targets of TCERG1. We found that targets of TCERG1 were enriched in microRNA-binding sites, suggesting the possibility of post-transcriptional regulation. Consistently, reverse transcription-PCR analysis revealed that many of the changes observed upon TCERG1 knockdown were because of differences in alternative mRNA processing of the 3′-untranslated regions. Furthermore, a novel computational approach, which can identify alternatively processed events from conventional microarray data, showed that TCERG1 led to widespread alterations in mRNA processing. These findings provide the strongest support to date for a role of TCERG1 in mRNA processing and are consistent with proposals that TCERG1 couples transcription and processing. © 2008 by The American Society for Biochemistry and Molecular Biology, Inc.
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Melen, G.J. - Pesce, C.G. - Rossi, M.S. - Kornblihtt, A.R.
EMBO J. 1999;18(11):3107-3118
1999
Temas: Mammalian cells - Ribosomal RNA processing - RNA 28s - RNA precursor - animal tissue - article - fibroblast culture - heart - intron - liver
Descripción: Splitting and apparent splicing of ribosomal RNA, both previously unknown in vertebrates, were found in rodents of the genus Ctenomys. Instead of being formed by a single molecule of 4.4 kb, 28S rRNA is split in two molecules of 2.6 and 1.8 kb. A hidden break, mapping within a 106 bp 'intron' located in the D6 divergent region, is expressed in mature ribosomes of liver, lung, heart and spleen, as well as in primary fibroblast cultures. Testis-specific processing eliminates the intron and concomitantly the break site, producing non-split 28S rRNA molecules exclusively in this organ. The intron is flanked by two 9 bp direct repeats, revealing the acquisition by insertion of a novel rRNA processing strategy in the evolution of higher organisms.
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Sala, C.D. - Soler-Bistué, A.J.C. - Korprapun, L. - Zorreguieta, A. - Tolmasky, M.E.
PLoS ONE 2012;7(10)
2012
Temas: messenger RNA - ribonuclease P - transfer RNA - article - bacterial cell - binding affinity - binding site - complex formation - controlled study - Escherichia coli
Descripción: EGS (external guide sequence) technology is a promising approach to designing new antibiotics. EGSs are short antisense oligoribonucleotides that induce RNase P-mediated cleavage of a target RNA by forming a precursor tRNA-like complex. The ftsZ mRNA secondary structure was modeled and EGSs complementary to two regions with high probability of being suitable targets were designed. In vitro reactions showed that EGSs targeting these regions bound ftsZ mRNA and elicited RNase P-mediated cleavage of ftsZ mRNA. A recombinant plasmid, pEGSb1, coding for an EGS that targets region "b" under the control of the T7 promoter was generated. Upon introduction of this plasmid into Escherichia coli BL21(DE3)(pLysS) the transformant strain formed filaments when expression of the EGS was induced. Concomitantly, E. coli harboring pEGSb1 showed a modest but significant inhibition of growth when synthesis of the EGSb1 was induced. Our results indicate that EGS technology could be a viable strategy to generate new antimicrobials targeting ftsZ. © 2012 Sala et al.
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Schwede, A. - Manful, T. - Jha, B.A. - Helbig, C. - Bercovich, N. - Stewart, M. - Clayton, C.
Nucleic Acids Res. 2009;37(16):5511-5528
2009
Temas: chromatin assembly factor 1 - gene product - messenger RNA - protein EP - ribosome protein - unclassified drug - EP procyclin protein, Trypanosoma brucei - membrane protein - mRNA deadenylase - phosphoglycerate kinase
Descripción: Removal of the poly(A) tail is the first step in the degradation of many eukaryotic mRNAs. In metazoans and yeast, the Ccr4/Caf1/Not complex has the predominant deadenylase activity, while the Pan2/Pan3 complex may trim poly(A) tails to the correct size, or initiate deadenylation. In trypanosomes, turnover of several constitutively-expressed or long-lived mRNAs is not affected by depletion of the 5'-3' exoribonuclease XRNA, but is almost completely inhibited by depletion of the deadenylase CAF1. In contrast, two highly unstable mRNAs, encoding EP procyclin and a phosphoglycerate kinase, PGKB, accumulate when XRNA levels are reduced. We here show that degradation of EP mRNA was partially inhibited after CAF1 depletion. RNAi-targeting trypanosome PAN2 had a mild effect on global deadenylation, and on degradation of a few mRNAs including EP. By amplifying and sequencing degradation intermediates, we demonstrated that a reduction in XRNA had no effect on degradation of a stable mRNA encoding a ribosomal protein, but caused accumulation of EP mRNA fragments that had lost substantial portions of the 5' and 3' ends. The results support a model in which trypanosome mRNAs can be degraded by at least two different, partially independent, cytoplasmic degradation pathways attacking both ends of the mRNA. © 2009 The Author(s).
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Kadener, S. - Fededa, J.P. - Rosbash, M. - Kornblihtt, A.R.
Proc. Natl. Acad. Sci. U. S. A. 2002;99(12):8185-8190
2002
Temas: Coupling - RNA processing - Transcription - alpha globin - cis acting element - fibronectin - RNA polymerase II - alternative RNA splicing - article - chromatin
Descripción: Promoters and enhancers are cis-acting elements that control gene transcription via complex networks of protein-DNA and proteinprotein interactions. Whereas promoters deal with putting in place the RNA polymerase, both enhancers and promoters can control transcriptional initiation and elongation. We have previously shown that promoter structure modulates alternative splicing, strengthening the concept of a physical and functional coupling between transcription and splicing. Here we report that the promoter effect is due to the control of RNA pol II elongation. We found that the simian virus 40 (SV40) transcriptional enhancer, inserted in fibronectin (FN) minigene constructs transfected into mammalian cells, controls alternative splicing by inhibiting inclusion of the FN extra domain I (EDI) exon into mature mRNA. Deletion analysis of enhancer subdomains and competitions in vivo with excess of specific enhancer DNA subfragments demonstrate that the "minimal" enhancer, consisting of two 72-bp repeats, is responsible for the splicing effect. The 72-bp repeat region has been reported to promote RNA pol II elongation. When transcription is driven by the α-globin promoter linked to the SV40 enhancer, basal EDI inclusion and activation by the SR (Ser-Arg-rich) protein SF2/ASF are much lower than with other promoters. Deletion of only one of the two 72-bp repeats not only provokes higher EDI inclusion levels but allows responsiveness to SF2/ASF. These effects are the consequence of a decrease in RNA pol II elongation evidenced both by an increase in the proportions of shorter proximal over full length transcripts and by higher pol II densities upstream of the alternative exon detected by chromatin immunoprecipitation.
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Nogués, G. - Kadener, S. - Cramer, P. - De la Mata, M. - Fededa, J.P. - Blaustein, M. - Srebrow, A. - Kornblihtt, A.R.
IUBMB Life 2003;55(4-5):235-241
2003
Temas: Alternative splicing - Elongation - mRNA processing - RNA polymerase II - Transcription - calcitonin gene related peptide - fibronectin - Hermes antigen - messenger RNA - protein
Descripción: The realization that the mammalian proteomic complexity is achieved with a limited number of genes demands a better understanding of alternative splicing regulation. Promoter control of alternative splicing was originally described by our group in studies performed on the fibronectin gene. Recently, other labs extended our findings to the cystic fibrosis, CD44 and CGRP genes strongly supporting a coupling between transcription and pre-mRNA splicing. A possible mechanism that would fit in these results is that the promoter itself is responsible for recruiting splicing factors, such as SR proteins, to the site of transcription, possibly through transcription factors that bind the promoter or the transcriptional enhancers. An alternative model, discussed more extensively in this review, involves modulation of RNA pol II (pol II) elongation rate. The model is supported by findings that cis- and trans-acting factors that modulate pol II elongation on a particular template also provoke changes in the alternative splicing balance of the encoded mRNAs.
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Pelisch, F. - Gerez, J. - Druker, J. - Schor, I.E. - Muñoz, M.J. - Risso, G. - Petrillo, E. - Westman, B.J. - Lamond, A.I. - Arzt, E. - Srebrow, A.
Proc. Natl. Acad. Sci. U. S. A. 2010;107(37):16119-16124
2010
Temas: E3 ligase - Posttranslational modification - RNA processing - Splicing factor - protein asf - protein inhibitor of activated STAT - protein inhibitor of activated STAT1 - protein sf2 - protein Ubc9 - regulator protein
Descripción: Protein modification by conjugation of small ubiquitin-related modifier (SUMO) is involved in diverse biological functions, such as transcription regulation, subcellular partitioning, stress response, DNA damage repair, and chromatin remodeling. Here, we show that the serine/arginine-rich protein SF2/ASF, a factor involved in splicing regulation and other RNA metabolism-related processes, is a regulator of the sumoylation pathway. The overexpression of this protein stimulates, but its knockdown inhibits SUMO conjugation. SF2/ASF interacts with Ubc9 and enhances sumoylation of specific substrates, sharing characteristics with already described SUMO E3 ligases. In addition, SF2/ASF interacts with the SUMO E3 ligase PIAS1 (protein inhibitor of activated STAT-1), regulating PIAS1-induced overall protein sumoylation. The RNA recognition motif 2 of SF2/ASF is necessary and sufficient for sumoylation enhancement. Moreover, SF2/ASF has a role in heat shock-induced sumoylation and promotes SUMO conjugation to RNA processing factors. These results add a component to the sumoylation pathway and a previously unexplored role for the multifunctional SR protein SF2/ASF.
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Schor, I.E. - Llères, D. - Risso, G.J. - Pawellek, A. - Ule, J. - Lamond, A.I. - Kornblihtt, A.R.
PLoS ONE 2012;7(11)
2012
Temas: enhanced green fluorescent protein - heterochromatin protein 1 - heterochromatin protein 1alpha - histone H3 - histone H4 - messenger RNA - nuclear protein - protein SRSF1 - protein SRSF2 - trichostatin A
Descripción: Chromatin structure is an important factor in the functional coupling between transcription and mRNA processing, not only by regulating alternative splicing events, but also by contributing to exon recognition during constitutive splicing. We observed that depolarization of neuroblastoma cell membrane potential, which triggers general histone acetylation and regulates alternative splicing, causes a concentration of SR proteins in nuclear speckles. This prompted us to analyze the effect of chromatin structure on splicing factor distribution and dynamics. Here, we show that induction of histone hyper-acetylation results in the accumulation in speckles of multiple splicing factors in different cell types. In addition, a similar effect is observed after depletion of the heterochromatic protein HP1α, associated with repressive chromatin. We used advanced imaging approaches to analyze in detail both the structural organization of the speckle compartment and nuclear distribution of splicing factors, as well as studying direct interactions between splicing factors and their association with chromatin in vivo. The results support a model where perturbation of normal chromatin structure decreases the recruitment efficiency of splicing factors to nascent RNAs, thus causing their accumulation in speckles, which buffer the amount of free molecules in the nucleoplasm. To test this, we analyzed the recruitment of the general splicing factor U2AF65 to nascent RNAs by iCLIP technique, as a way to monitor early spliceosome assembly. We demonstrate that indeed histone hyper-acetylation decreases recruitment of U2AF65 to bulk 3′ splice sites, coincident with the change in its localization. In addition, prior to the maximum accumulation in speckles, ~20% of genes already show a tendency to decreased binding, while U2AF65 seems to increase its binding to the speckle-located ncRNA MALAT1. All together, the combined imaging and biochemical approaches support a model where chromatin structure is essential for efficient co-transcriptional recruitment of general and regulatory splicing factors to pre-mRNA. © 2012 Schor et al.
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Rocha-Viegas, L. - Vicent, G.P. - Barañao, J.L. - Beato, M. - Pecci, A.
J. Biol. Chem. 2006;281(45):33959-33970
2006
Temas: Derivatives - Enzyme inhibition - Genes - Hormones - RNA - Tissue - Cell death - Hormonal treatment - Lymphoid cells - Thymocytes
Descripción: The bcl-X gene plays a critical role in apoptosis. Six different isoforms generated by tissue-specific promoter usage and alternative splicing were described. Some of them exert opposite effects on cell death. In mammary epithelial cells glucocorticoids induce bcl-X expression and increase the ratio bcl-XL (antiapoptotic)/bcl-XS (apoptotic) by activating P4 promoter, which contains two hormone response elements. Here we show that, on mouse thymocytes and T lymphocyte derivative S49 cells, glucocorticoids inhibited transcription from P4 and decreased the ratio bcl-X L/bcl-XS favoring apoptosis. Upon hormonal treatment, glucocorticoid receptor (GR), steroid receptor coactivator-1, and RNA polymerase II were transiently recruited to P4 promoter, whereas STAT5B was also recruited but remained bound. Concomitant with the release of GR, silencing mediator for retinoic acid receptor and thyroid hormone receptor and histone deacetylase 3 were recruited, histone H3 was deacetylated, and RNA polymerase II left the promoter. Inhibition of STAT5 activity reverted glucocorticoid repression to activation of transcription and was accompanied by stable recruitment of GR and RNA polymerase II to P4. © 2006 by The American Society for Biochemistry and Molecular Biology, Inc.
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De La Mata, M. - Alonso, C.R. - Kadener, S. - Fededa, J.P. - Blaustein, M. - Pelisch, F. - Cramer, P. - Bentley, D. - Kornblihtt, A.R.
Mol. Cell 2003;12(2):525-532
2003
Temas: elongation factor - fibronectin - protein subunit - RNA - RNA polymerase II - Adenovirus - article - cell culture - Drosophila - embryo cell
Descripción: Changes in promoter structure and occupation have been shown to modify the splicing pattern of several genes, evidencing a coupling between transcription and alternative splicing. It has been proposed that the promoter effect involves modulation of RNA pol II elongation rates. The C4 point mutation of the Drosophila pol II largest subunit confers on the enzyme a lower elongation rate. Here we show that expression of a human equivalent to Drosophila's C4 pol II in human cultured cells affects alternative splicing of the fibronectin EDI exon and adenovirus E1a pre-mRNA. Most importantly, resplicing of the Hox gene Ultrabithorax is stimulated in Drosophila embryos mutant for C4, which demonstrates the transcriptional control of alternative splicing on an endogenous gene. These results provide a direct proof for the elongation control of alternative splicing in vivo.
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Abrahamyan, L.G. - Chatel-Chaix, L. - Ajamian, L. - Milev, M.P. - Monette, A. - Clément, J.-F. - Song, R. - Lehmann, M. - DesGroseillers, L. - Laughrea, M. - Boccaccio, G. - Mouland, A.J.
J. Cell Sci. 2010;123(3):369-383
2010
Temas: AIDS - HIV-1 - Intracellular traffic - Ribonucleoprotein - RNA encapsidation - SHRNP - sIRNA - Staufen1 - Staufen1 HIV-1-dependent RNP - Virus-host interaction
Descripción: Human immunodeficiency virus type 1 (HIV-1) Gag selects for and mediates genomic RNA (vRNA) encapsidation into progeny virus particles. The host protein, Staufen1 interacts directly with Gag and is found in ribonucleoprotein (RNP) complexes containing vRNA, which provides evidence that Staufen1 plays a role in vRNA selection and encapsidation. In this work, we show that Staufen1, vRNA and Gag are found in the same RNP complex. These cellular and viral factors also colocalize in cells and constitute novel Staufen1 RNPs (SHRNPs) whose assembly is strictly dependent on HIV-1 expression. SHRNPs are distinct from stress granules and processing bodies, are preferentially formed during oxidative stress and are found to be in equilibrium with translating polysomes. Moreover, SHRNPs are stable, and the association between Staufen1 and vRNA was found to be evident in these and other types of RNPs. We demonstrate that following Staufen1 depletion, apparent supraphysiologic-sized SHRNP foci are formed in the cytoplasm and in which Gag, vRNA and the residual Staufen1 accumulate. The depletion of Staufen1 resulted in reduced Gag levels and deregulated the assembly of newly synthesized virions, which were found to contain several-fold increases in vRNA, Staufen1 and other cellular proteins. This work provides new evidence that Staufen1-containing HIV-1 RNPs preferentially form over other cellular silencing foci and are involved in assembly, localization and encapsidation of vRNA.
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Landau, A.M. - Lokstein, H. - Scheller, H.V. - Lainez, V. - Maldonado, S. - Prina, A.R.
Plant Physiol. 2009;151(4):1802-1811
2009
Temas: messenger RNA - pigment - plant extract - vegetable protein - article - barley - chloroplast - cytoplasm - gene expression regulation - genetics
Descripción: A cytoplasmically inherited chlorophyll-deficient mutant of barley (Hordeum vulgare) termed cytoplasmic line 3 (CL3), displaying a viridis (homogeneously light-green colored) phenotype, has been previously shown to be affected by elevated temperatures. In this article, biochemical, biophysical, and molecular approaches were used to study the CL3 mutant under different temperature and light conditions. The results lead to the conclusion that an impaired assembly of photosystem I (PSI) under higher temperatures and certain light conditions is the primary cause of the CL3 phenotype. Compromised splicing of ycf3 transcripts, particularly at elevated temperature, resulting from a mutation in a noncoding region (intron 1) in the mutant ycf3 gene results in a defective synthesis of Ycf3, which is a chaperone involved in PSI assembly. The defective PSI assembly causes severe photoinhibition and degradation of PSII. © 2009 American Society of Plant Biologists.
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Alló, M. - Schor, I.E. - Muñoz, M.J. - De La Mata, M. - Agirre, E. - Valcárcel, J. - Eyras, E. - Kornblihtt, A.R.
Cold Spring Harbor Symp. Quant. Biol. 2010;75:103-111
2010
Temas: double stranded RNA - fibronectin - messenger RNA - mitogen activated protein kinase - nerve cell adhesion molecule - polypyrimidine tract binding protein - RNA polymerase II - small interfering RNA - trichostatin A - histone
Descripción: Alternative splicing affects more than 90% of human genes. Coupling between transcription and splicing has become crucial in the complex network underlying alternative splicing regulation. Because chromatin is the real template for nuclear transcription, changes in its structure, but also in the "reading" and "writing" of the histone code, could modulate splicing choices. Here, we discuss the evidence supporting these ideas, from the first proposal of chromatin affecting alternative splicing, performed 20 years ago, to the latest findings including genome-wide evidence that nucleosomes are preferentially positioned in exons. We focus on two recent reports from our laboratories that add new evidence to this field. The first report shows that a physiological stimulus such as neuron depolarization promotes intragenic histone acetylation (H3K9ac) and chromatin relaxation, causing the skipping of exon 18 of the neural cell adhesion molecule gene. In the second report, we show how specific histone modifications can be created at targeted gene regions as a way to affect alternative splicing: Using small interfering RNAs (siRNAs), we increased the levels of H3K9me2 and H3K27me3 in the proximity of alternative exon 33 of the human fibronectin gene, favoring its inclusion into mature messenger RNA (mRNA) through a mechanism that recalls RNAmediated transcriptional gene silencing. © 2010 Cold Spring Harbor Laboratory Press.
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Maeto, C.A. - Knott, M.E. - Linero, F.N. - Ellenberg, P.C. - Scolaro, L.A. - Castilla, V.
J. Gen. Virol. 2011;92(9):2181-2190
2011
Temas: cell protein - ribonucleoprotein - ribonucleoprotein A1 - ribonucleoprotein A2 - ribonucleoprotein B - small interfering RNA - unclassified drug - virus nucleoprotein - Argentine hemorrhagic fever - article
Descripción: Heterogeneous nuclear ribonucleoproteins A and B (hnRNPs A/B), cellular RNA-binding proteins that participate in splicing, trafficking, translation and turnover of mRNAs, have been implicated in the life cycles of several cytoplasmic RNA viruses. Here, we demonstrate that silencing of hnRNPs A1 and A2 significantly reduces the replication of the arenavirus Juni{dotless} ́n virus (JUNV), the aetiological agent of Argentine haemorrhagic fever. While acute JUNV infection did not modify total levels of expression of hnRNPs A/B in comparison with uninfected cells, non-cytopathic persistent infection exhibited low levels of these cell proteins. Furthermore, acutely infected cells showed a cytoplasmic relocalization of overexpressed hnRNP A1, probably related to the involvement of this protein in virus replicative cycle. This cytoplasmic accumulation was also observed in cells expressing viral nucleoprotein (N), and co-immunoprecipitation studies revealed the interaction between hnRNP A1 and N protein. By contrast, a predominantly nuclear distribution of overexpressed hnRNP A1 was found during persistent infection, even in the presence of endogenous or overexpressed N protein, indicating a differential modulation of nucleo-cytoplasmic trafficking in acute and persistent JUNV infections. © 2011 SGM.
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Mascanfroni, I.D. - Montesinos, M.D.M. - Alamino, V.A. - Susperreguy, S. - Nicola, J.P. - Ilarregui, J.M. - Masini-Repiso, A.M. - Rabinovich, G.A. - Pellizas, C.G.
J. Biol. Chem. 2010;285(13):9569-9582
2010
Temas: Adaptive immunity - AKT activation - Akt phosphorylation - Chromatin immunoprecipitation analysis - Dendritic cells - Endocrine systems - Mechanism control - Nuclear factors - Phosphatidylinositol 3-kinase - Promoter region
Descripción: Despite considerable progress in our understanding of the interplay between immune and endocrine systems, the role of thyroid hormones and their receptors in the control of adaptive immunity is still uncertain. Here, we investigated the role of thyroid hormone receptor (TR) β 1 signaling in modulating dendritic cell (DC) physiology and the intracellular mechanisms underlying these immunoregulatory effects. Exposure of DCs to triiodothyronine (T 3 ) resulted in a rapid and sustained increase in Akt phosphorylation independently of phosphatidylinositol 3-kinase activation, which was essential for supporting T 3 -induced DC maturation and interleukin (IL)-12 production. This effect was dependent on intact TRβ 1 signaling as small interfering RNA-mediated silencing of TRβ 1 expression prevented T 3 -induced DC maturation and IL-12 secretion as well as Akt activation and IκB-ε degradation. In turn, T 3 up-regulated TRβ 1 expression through mechanisms involving NF-κB, suggesting an autocrine regulatory loop to control hormone-dependent TRβ 1 signaling. These findings were confirmed by chromatin immunoprecipitation analysis, which disclosed a new functional NF-κB consensus site in the promoter region of the TRB1 gene. Thus, a T 3 -induced NF-κB-dependent mechanism controls TRβ 1 expression, which in turn signals DCs to promote maturation and function via an Akt-dependent but PI3K-independent pathway. These results underscore a novel unrecognized target that regulates DC maturation and function with critical implications in immunopathology at the crossroads of the immune-endocrine circuits. © 2010 by The American Society for Biochemistry and Molecular Biology, Inc.
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