RESUMEN
The cascade that culminates in macrometastases is thought to be mediated by phenotypic plasticity, including epithelial-mesenchymal and mesenchymal-epithelial transitions (EMT and MET). Although there is substantial support for the role of EMT in driving cancer cell invasion and dissemination, much less is known about the importance of MET in the later steps of metastatic colonization. We created novel reporters, which integrate transcriptional and post-transcriptional regulation, to test whether MET is required for metastasis in multiple in vivo cancer models. In a model of carcinosarcoma, metastasis occurred via an MET-dependent pathway; however, in two prostate carcinoma models, metastatic colonization was MET independent. Our results provide evidence for both MET-dependent and MET-independent metastatic pathways.
Asunto(s)
Transición Epitelial-Mesenquimal , Metástasis de la Neoplasia , Animales , Proliferación Celular , Femenino , Humanos , Ratones , Ratones Endogámicos BALB C , Neoplasias/patologíaRESUMEN
The brain serotonergic system has an essential role in the physiological functions of the central nervous system and dysregulation of serotonin (5-HT) homeostasis has been implicated in many neuropsychiatric disorders. The tryptophan hydroxylase-2 (TPH2) gene is the rate-limiting enzyme in brain 5-HT synthesis, and thus is an ideal candidate gene for understanding the role of dysregulation of brain serotonergic homeostasis. Here, we characterized a common, but functional single-nucleotide polymorphism (SNP rs1386493) in the TPH2 gene, which decreases efficiency of normal RNA splicing, resulting in a truncated TPH2 protein (TPH2-TR) by alternative splicing. TPH2-TR, which lacks TPH2 enzyme activity, dominant-negatively affects full-length TPH2 function, causing reduced 5-HT production. The predicted mRNA for TPH2-TR is present in postmortem brain of rs1386493 carriers. The rs13864923 variant does not appear to be overrepresented in either global or multiplex depression cohorts. However, in combination with other gene variants linked to 5-HT homeostasis, this variant may exhibit important epistatic influences.
Asunto(s)
Empalme Alternativo , Depresión/genética , Predisposición Genética a la Enfermedad/genética , Serotonina/biosíntesis , Triptófano Hidroxilasa/genética , Animales , Tronco Encefálico/metabolismo , Línea Celular Transformada , Femenino , Predisposición Genética a la Enfermedad/psicología , Genotipo , Humanos , Masculino , Células PC12 , Linaje , Polimorfismo de Nucleótido Simple/genética , RatasRESUMEN
CA150 represses RNA polymerase II (RNAPII) transcription by inhibiting the elongation of transcripts. The FF repeat domains of CA150 bind directly to the phosphorylated carboxyl-terminal domain of the largest subunit of RNAPII. We determined that this interaction is required for efficient CA150-mediated repression of transcription from the alpha(4)-integrin promoter. Additional functional determinants, namely, the WW1 and WW2 domains of CA150, were also required for efficient repression. A protein that interacted directly with CA150 WW1 and WW2 was identified as the splicing-transcription factor SF1. Previous studies have demonstrated a role for SF1 in transcription repression, and we found that binding of the CA150 WW1 and WW2 domains to SF1 correlated exactly with the functional contribution of these domains for repression. The binding specificity of the CA150 WW domains was found to be unique in comparison to known classes of WW domains. Furthermore, the CA150 binding site, within the carboxyl-terminal half of SF1, contains a novel type of proline-rich motif that may be recognized by the CA150 WW1 and WW2 domains. These results support a model for the recruitment of CA150 to repress transcription elongation. In this model, CA150 binds to the phosphorylated CTD of elongating RNAPII and SF1 targets the nascent transcript.
Asunto(s)
Proteínas de Unión al ADN , ARN Polimerasa II/metabolismo , Precursores del ARN/metabolismo , Empalme del ARN , Proteínas de Unión al ARN/metabolismo , Proteínas Represoras/metabolismo , Transactivadores/metabolismo , Factores de Transcripción , Secuencia de Aminoácidos , Sitios de Unión , Línea Celular Transformada , Regulación de la Expresión Génica , Células HeLa , Humanos , Datos de Secuencia Molecular , Fosforilación , Prolina/metabolismo , Factores de Empalme de ARN , Proteínas de Unión al ARN/genética , Proteínas Represoras/genética , Relación Estructura-Actividad , Transactivadores/genética , Factores de Elongación TranscripcionalRESUMEN
Nascent transcripts are the true substrates for many splicing events in mammalian cells. In this review we discuss transcription, splicing, and alternative splicing in the context of co-transcriptional processing of pre-mRNA. The realization that splicing occurs co-transcriptionally requires two important considerations: First, the cis-acting elements in the splicing substrate are synthesized at different times in a 5' to 3' direction. This dynamic view of the substrate implies that in a 100 kb intron the 5' splice site will be synthesized as much as an hour before the 3' splice site. Second, the transcription machinery and the splicing machinery, which are both complex and very large, are working in close proximity to each other. It is therefore likely that these two macromolecular machines interact, and recent data supporting this notion is discussed. We propose a model for co-transcriptional pre-mRNA processing that incorporates the concepts of splice site-tethering and dynamic exon definition. Also, we present a dynamic view of the alternative splicing of FGF-R2 and suggest that this view could be generally applicable to many regulated splicing events.
Asunto(s)
Empalme Alternativo , Precursores del ARN/genética , Transcripción Genética/genética , Animales , Humanos , Modelos Biológicos , ARN Polimerasa II/metabolismo , Precursores del ARN/metabolismo , ARN Mensajero/genética , ARN Mensajero/metabolismoRESUMEN
The functional repertoire of the human genome is amplified by the differential assortment of exons. Spliceosome-mediated RNA trans-splicing can mobilize these packets of genetic information to reprogram mRNAs. In principle, this process could repair defective transcripts in loss-of-function genetic disorders in humans. We developed a tractable lacZ repair system to serve as a model for these genetic disorders. Targeted pre-trans-splicing RNA molecules efficiently and specifically repaired mutated lacZ transcripts and restored enzymatic activity in human cells. The development of this model confirms the potential for spliceosome-mediated RNA trans-splicing in genetic repairs and provides a powerful tool for rational design and in vitro evolution of pre-trans-splicing molecules.
Asunto(s)
Operón Lac , Empalme del ARN/fisiología , ARN Mensajero/genética , Empalmosomas/metabolismo , Fraccionamiento Celular , Línea Celular , Regulador de Conductancia de Transmembrana de Fibrosis Quística/genética , Humanos , Immunoblotting , Reacción en Cadena de la Polimerasa/métodos , ARN Mensajero/metabolismo , Transfección , beta-Galactosidasa/metabolismoAsunto(s)
Proteínas de Unión al ARN/genética , Ribonucleoproteínas/genética , Empalme Alternativo , Secuencia de Aminoácidos , Animales , Exones/genética , Humanos , Intrones/genética , Datos de Secuencia Molecular , Proteína de Unión al Tracto de Polipirimidina , ARN Mensajero/genética , Alineación de SecuenciaRESUMEN
Alternative splicing of fibroblast growth factor receptor 2 (FGF-R2) transcripts involves the mutually exclusive usage of exons IIIb and IIIc to produce two different receptor isoforms. Appropriate splicing of exon IIIb in rat prostate cancer DT3 cells requires a previously described cis element (ISAR, for "intronic splicing activator and repressor") which represses the splicing of exon IIIc and activates the splicing of exon IIIb. This element is nonfunctional in rat prostate AT3 cells, which repress exon IIIb inclusion and splice to exon IIIc. We have now identified an intronic element upstream of exon IIIb that causes repression of exon IIIb splicing. Deletion of this element abrogates the requirement for ISAR in order for exon IIIb to be spliced in DT3 cells and causes inappropriate inclusion of exon IIIb in AT3 cells. This element consists of two intronic splicing silencer (ISS) sequences, ISS1 and ISS2. The ISS1 sequence is pyrimidine rich, and in vitro cross-linking studies demonstrate binding of polypyrimidine tract binding protein (PTB) to this element. Competition studies demonstrate that mutations within ISS1 that abolish PTB binding in vitro alleviate splicing repression in vivo. Cotransfection of a PTB-1 expression vector with a minigene containing exon IIIb and the intronic splicing silencer element demonstrate PTB-mediated repression of exon IIIb splicing. Furthermore, all described PTB isoforms were equally capable of mediating this effect. Our results support a model of splicing regulation in which exon IIIc splicing does not represent a default splicing pathway but rather one in which active repression of exon IIIb splicing occurs in both cells and in which DT3 cells are able to overcome this repression in order to splice exon IIIb.
Asunto(s)
Empalme Alternativo/genética , Proteínas de Unión al ADN/fisiología , Exones/genética , Silenciador del Gen , Intrones/genética , Proteínas de Unión al ARN/fisiología , Proteínas Tirosina Quinasas Receptoras/genética , Receptores de Factores de Crecimiento de Fibroblastos/genética , Adenocarcinoma/genética , Adenocarcinoma/patología , Animales , Regulación Neoplásica de la Expresión Génica , Masculino , Mutagénesis Sitio-Dirigida , Proteínas de Neoplasias/biosíntesis , Proteínas de Neoplasias/genética , Reacción en Cadena de la Polimerasa , Proteína de Unión al Tracto de Polipirimidina , Neoplasias de la Próstata/genética , Neoplasias de la Próstata/patología , Precursores del ARN/metabolismo , ARN Neoplásico/metabolismo , Ratas , Receptor Tipo 2 de Factor de Crecimiento de Fibroblastos , Proteínas Recombinantes de Fusión/genética , Proteínas Recombinantes de Fusión/fisiología , Secuencias Reguladoras de Ácidos Nucleicos , Eliminación de Secuencia , Células Tumorales CultivadasRESUMEN
In Saccharomyces cerevisiae, Prp17p is required for the efficient completion of the second step of pre-mRNA splicing. The function and interacting factors for this protein have not been elucidated. We have performed a mutational analysis of yPrp17p to identify protein domains critical for function. A series of deletions were made throughout the region spanning the N-terminal 158 amino acids of the protein, which do not contain any identified structural motifs. The C-terminal portion (amino acids 160-455) contains a WD domain containing seven WD repeats. We determined that a minimal functional Prp17p consists of the WD domain and 40 amino acids N-terminal to it. We generated a three-dimensional model of the WD repeats in Prp17p based on the crystal structure of the beta-transducin WD domain. This model was used to identify potentially important amino acids for in vivo functional characterization. Through analysis of mutations in four different loops of Prp17p that lie between beta strands in the WD repeats, we have identified four amino acids, 235TETG238, that are critical for function. These amino acids are predicted to be surface exposed and may be involved in interactions that are important for splicing. Temperature-sensitive prp17 alleles with mutations of these four amino acids are defective for the second step of splicing and are synthetically lethal with a U5 snRNA loop I mutation, which is also required for the second step of splicing. These data reinforce the functional significance of this region within the WD domain of Prp17p in the second step of splicing.
Asunto(s)
Proteínas de Ciclo Celular , Proteínas de Unión al ADN , Proteínas Fúngicas/química , ARN Nuclear Pequeño/metabolismo , Proteínas de Unión al ARN , Secuencia de Aminoácidos , Western Blotting , Análisis Mutacional de ADN , Proteínas Fúngicas/genética , Proteínas Fúngicas/fisiología , Humanos , Modelos Moleculares , Datos de Secuencia Molecular , Señales de Localización Nuclear/genética , Conformación de Ácido Nucleico , Conformación Proteica , Precursores del ARN/metabolismo , Factores de Empalme de ARN , ARN Nuclear Pequeño/química , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Saccharomyces cerevisiae , Homología de Secuencia de AminoácidoRESUMEN
Compelling in vivo studies suggest a tight functional linkage between RNA polymerase II transcription and premessenger RNA splicing. At present, the specific interactions involved in this coupling are poorly understood and deserve investigation. To this end, we developed an in vitro system that permits study of coupled transcription and splicing. Transcripts generated by RNA polymerase II were accurately and efficiently spliced under reaction conditions that permitted both transcription and splicing to occur simultaneously. The splicing of RNA-polymerase-II-driven transcripts was accelerated relative to that of the same transcripts driven by T7 RNA polymerase. Moreover, the product of exon ligation was found associated with the DNA template in reactions driven by RNA polymerase II. These two findings indicate that transcription and splicing were coupled in the in vitro system driven by RNA polymerase II, and suggest that this system will be useful for the biochemical study of this coupling.
Asunto(s)
ARN Polimerasa II/genética , Precursores del ARN/metabolismo , Empalme del ARN/fisiología , Secuencia de Bases , ADN Viral/genética , VIH-1/genética , Células HeLa , Humanos , Datos de Secuencia Molecular , ARN Polimerasa II/metabolismo , Transcripción GenéticaRESUMEN
Equine infectious anemia virus (EIAV) activates transcription via a Tat protein, a TAR element, and the equine elongation factor positive transcription elongation factor b (P-TEFb). In human cells, EIAV Tat (eTat) can inhibit the ability of human immunodeficiency virus type 1 (HIV-1) Tat (hTat) to activate transcription from the HIV-1 long terminal repeat, demonstrating that EIAV Tat can interact nonproductively with human P-TEFb. To study the mechanism of EIAV Tat and HIV-1 Tat activation, we developed an in vitro elongation assay that recapitulates EIAV Tat-mediated inhibition of HIV-1 Tat trans-activation. We found that eTat specifically inhibits activation of elongation by HIV-1 Tat while having no effect on basal transcription elongation. The competitive inhibition of hTat activation was reversed by an activity present in HeLa cell nuclear extracts, most likely a form of P-TEFb. Recombinant P-TEFb (cyclin T1 and CDK9) overcame the inhibition of transcription by eTat but in a nonspecific manner. EIAV Tat affinity chromatography was used to purify the activity present in nuclear extract that was capable of reversing eTat inhibition. We characterized the protein components of this activity, which include cyclin T1, CDK9, Tat-SF1, and at least three unidentified proteins. These data suggest that additional factors are involved in the mechanism of Tat activation.
Asunto(s)
Regulación Viral de la Expresión Génica , Productos del Gen tat/antagonistas & inhibidores , Productos del Gen tat/metabolismo , VIH-1/genética , Virus de la Anemia Infecciosa Equina , Proteínas Serina-Treonina Quinasas/metabolismo , Unión Competitiva , Extractos Celulares , Sistema Libre de Células , Cromatografía de Afinidad , Ciclina T , Quinasa 9 Dependiente de la Ciclina , Quinasas Ciclina-Dependientes/aislamiento & purificación , Quinasas Ciclina-Dependientes/metabolismo , Ciclinas/aislamiento & purificación , Ciclinas/metabolismo , Productos del Gen tat/aislamiento & purificación , Duplicado del Terminal Largo de VIH/genética , Células HeLa , Calor , Humanos , Proteínas Nucleares/aislamiento & purificación , Proteínas Nucleares/metabolismo , Factor B de Elongación Transcripcional Positiva , Regiones Promotoras Genéticas/genética , Unión Proteica , Desnaturalización Proteica , Proteínas Recombinantes/antagonistas & inhibidores , Proteínas Recombinantes/aislamiento & purificación , Proteínas Recombinantes/metabolismo , Especificidad por Sustrato , Moldes Genéticos , Factores de Tiempo , Transactivadores/aislamiento & purificación , Transactivadores/metabolismo , Transcripción Genética/genética , Activación Transcripcional , Productos del Gen tat del Virus de la Inmunodeficiencia HumanaRESUMEN
An approach for purifying nuclear proteins that bind directly to the hyperphosphorylated C-terminal repeat domain (CTD) of RNA polymerase II was developed and used to identify one human phosphoCTD-associating protein as CA150. CA150 is a nuclear factor implicated in transcription elongation. Because the hyperphosphorylated CTD is a feature of actively transcribing RNA polymerase II (Pol II), phosphoCTD (PCTD) binding places CA150 in a location appropriate for performing a role in transcription elongation-related events. Several recombinant segments of CA150 bound the PCTD. Predominant binding is mediated by the portion of CA150 containing six FF domains, compact modules of previously unknown function. In fact, small recombinant proteins containing the fifth FF domain bound the PCTD. PCTD binding is the first specific function assigned to an FF domain. As FF domains are found in a variety of nuclear proteins, it is likely that some of these proteins are also PCTD-associating proteins. Thus FF domains appear to be compact protein-interaction modules that, like WW domains, can be evolutionarily shuffled to organize nuclear function.
Asunto(s)
ARN Polimerasa II/metabolismo , Transactivadores/metabolismo , Secuencia de Bases , Núcleo Celular/metabolismo , Cartilla de ADN , Células HeLa , Humanos , Fosforilación , Unión Proteica , Factores de Elongación TranscripcionalRESUMEN
Human immunodeficiency virus-1 Tat protein and human Cyclin T1 mediate transcriptional activation by enhancing the elongation efficiency of RNA polymerase II. Activation of transcription of the related equine infectious anemia virus (EIAV) requires a similar protein known as eTat, which does not function in human cells. Expression of equine Cyclin T1 in human cells rescues eTat function, suggesting a general mechanism of transcription activation among lentiviruses. Here we present the cloning of Cyclin T1 from canine D17 osteosarcoma cells, which support EIAV transactivation, and show that canine Cyclin T1 confers eTat transactivation to human cells. A two-amino-acid change, from 79-proline-glycine-80 to 79-histidine-arginine-80, confers on the human Cyclin T1 the ability to cooperate with eTat in transcriptional activation. These findings suggested that the regions of Cyclin T1 that interact with lentiviral Tat proteins and TAR RNA elements form an extended domain, which very likely has a conserved fold.
Asunto(s)
Ciclinas/metabolismo , Productos del Gen tat/genética , Productos del Gen tat/metabolismo , Virus de la Anemia Infecciosa Equina/genética , Activación Transcripcional , Secuencia de Aminoácidos , Animales , Clonación Molecular , Ciclina T , Ciclinas/química , Ciclinas/genética , Perros , Humanos , Virus de la Anemia Infecciosa Equina/metabolismo , Ratones , Datos de Secuencia Molecular , ARN Viral/genética , Elementos de Respuesta/genética , Secuencias Repetidas Terminales/genética , Células Tumorales CultivadasRESUMEN
Most messenger RNA precursors (pre-mRNA) undergo cis-splicing in which introns are excised and the adjoining exons from a single pre-mRNA are ligated together to form mature messenger RNA. This reaction is driven by a complex known as the spliceosome. Spliceosomes can also combine sequences from two independently transcribed pre-mRNAs in a process known as trans-splicing. Spliceosome-mediated RNA trans-splicing (SMaRT) is an emerging technology in which RNA pre-therapeutic molecules (PTMs) are designed to recode a specific pre-mRNA by suppressing cis-splicing while enhancing trans-splicing between the PTM and its pre-mRNA target. This study examined the feasibility of SMaRT as a potential therapy for genetic diseases to correct mutations using cystic fibrosis (CF) as an example. We used several versions of a cystic fibrosis transmembrane conductance regulator (CFTR) mini-gene expressing mutant (deltaF508) pre-mRNA targets and tested this against a number of PTMs capable of binding to the CFTR target intron 9 and trans-splicing in the normal coding sequences for exons 10-24 (containing F508). When 293T cells were cotransfected with both constructs, they produced a trans-spliced mRNA in which normal exon 10-24 replaced mutant exon 10. To test whether SMaRT produced mature CFTR protein, proteins were immunoprecipitated from lysates of cotransfected cells and detected by Western blotting and PKA-phosphorylation. Tryptic phosphopeptide mapping confirmed the identity of CFTR. This proof-of-concept study demonstrates that exon replacement by SMaRT can repair an abnormal pre-mRNA associated with a genetic disease.
Asunto(s)
Regulador de Conductancia de Transmembrana de Fibrosis Quística/genética , Fibrosis Quística/terapia , Terapia Genética/métodos , Precursores del ARN/genética , Western Blotting , Resinas de Intercambio de Catión , Línea Celular , Colon/citología , Regulador de Conductancia de Transmembrana de Fibrosis Quística/análisis , Exones , Estudios de Factibilidad , Ingeniería Genética/métodos , Humanos , Riñón/embriología , Lípidos , Sitios de Empalme de ARN , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Empalmosomas/genética , Transfección/métodosAsunto(s)
Precursores del ARN/análisis , Empalme del ARN/genética , Empalmosomas/química , Autorradiografía , Cromatografía de Afinidad , Cromatografía en Gel , Electroforesis en Gel Bidimensional , Electroforesis en Gel de Poliacrilamida , Células HeLa , Humanos , Sustancias Macromoleculares , Ribonucleoproteínas Nucleares Pequeñas/análisis , Transcripción Genética , UltracentrifugaciónRESUMEN
Tat protein strongly activates transcription from the human immunodeficiency virus type 1 (HIV-1) long terminal repeat (LTR) by enhancing the elongation efficiency of RNA polymerase II complexes. Tat-mediated transcriptional activation requires cellular cofactors and specific cis-acting elements within the HIV-1 promoter, among them a functional TATA box. Here, we have investigated the mechanism by which one of these cofactors, termed CA150, regulates HIV-1 transcription in vivo. We present a series of functional assays that demonstrate that the regulation of the HIV-1 LTR by CA150 has the same functional requirements as the activation by Tat. We found that CA150 affects elongation of transcription complexes assembled on the HIV-1 promoter in a TATA-box-dependent manner. We discuss the data in terms of the involvement of CA150 in the regulation of Tat-activated HIV-1 gene expression. In addition, we also provide evidence suggesting a role for CA150 in the regulation of cellular transcriptional processes.
Asunto(s)
Regulación Viral de la Expresión Génica , Duplicado del Terminal Largo de VIH , VIH-1/genética , ARN Polimerasa II/metabolismo , TATA Box , Transactivadores/metabolismo , Línea Celular Transformada , Proteínas de Unión al ADN/genética , Productos del Gen tat/metabolismo , Humanos , Regiones Promotoras Genéticas , Proteína de Unión a TATA-Box , Transactivadores/genética , Factores de Transcripción/genética , Transcripción Genética , Factores de Elongación Transcripcional , Productos del Gen tat del Virus de la Inmunodeficiencia HumanaRESUMEN
In this report we present evidence for a novel switch in the ratio of the two major isoforms of the polypyrimidine tract binding protein (PTB) in two related prostate cancer cell lines. The existence of different isoforms of PTB is thought to be the result of alternative splicing. We used UV cross-linking to identify a PTB doublet in the DT3 cell line, which is a rat prostate epithelial cancer line that is androgen-dependent and nonmetastatic. The AT3 cell line, a metastatic, androgen-independent cell line derived from the same tumor as the DT3 cells, was noted here to have a different isoform ratio of PTB. The two most prevalent isoforms of PTB were found to bind to an RNA probe containing a pyrimidine stretch. Western blot analysis demonstrated that these isoforms are indeed expressed differently in the two cell lines and that the observed binding is the result of this differential expression. These two cell lines are derived from the original Dunning prostate tumor, which is a model for studying tumor progression in the prostate. This ratio switch may be an important event in tumor progression in this model system of prostate cancer.
Asunto(s)
Empalme Alternativo , Neoplasias de la Próstata/química , Proteínas de Unión al ARN/análisis , Ribonucleoproteínas/análisis , Secuencia de Aminoácidos , Animales , Humanos , Masculino , Datos de Secuencia Molecular , Proteína de Unión al Tracto de Polipirimidina , Pruebas de Precipitina , Isoformas de Proteínas , Proteínas de Unión al ARN/genética , Ratas , Ribonucleoproteínas/genética , Células Tumorales CultivadasRESUMEN
We have developed RNA molecules capable of effecting spliceosome-mediated RNA trans-splicing reactions with a target messenger RNA precursor (pre-mRNA). Targeted trans-splicing was demonstrated in a HeLa nuclear extract, cultured human cells, and H1299 human lung cancer tumors in athymic mice. Trans-splicing between a cancer-associated pre-mRNA encoding the beta-subunit of human chorionic gonadotropin gene 6 and pre-trans-splicing molecule (PTM) RNA was accurate both in vitro and in vivo. Comparison of targeted versus nontargeted trans-splicing revealed a moderate level of specificity, which was improved by the addition of an internal inverted repeat encompassing the PTM splice site. Competition between cis- and trans-splicing demonstrated that cis-splicing can be inhibited by trans-splicing. RNA repair in a splicing model of a nonfunctional lacZ transcript was effected in cells by a PTM, which restored significant beta-galactosidase activity. These observations suggest that spliceosome-mediated RNA trans-splicing may represent a general approach for reprogramming the sequence of targeted transcripts, providing a novel approach to gene therapy.
Asunto(s)
Ingeniería Genética , Terapia Genética , Empalme del ARN/fisiología , Empalmosomas/genética , Animales , Gonadotropina Coriónica Humana de Subunidad beta/genética , Cartilla de ADN , Exones , Globinas/genética , Células HeLa , Humanos , Ratones , Ratones Desnudos , Modelos Biológicos , Neoplasias Experimentales , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Análisis de Secuencia de ADN , Factores de Tiempo , Transfección , Células Tumorales Cultivadas , beta-Galactosidasa/metabolismoRESUMEN
The human immunodeficiency virus type 1 (HIV-1) Tat protein is a transcriptional activator that is essential for efficient viral gene expression and replication. Tat increases the level of full-length transcripts from the HIV-1 promoter by dramatically enhancing the elongation efficiency of the RNA polymerase II complexes assembled on this promoter. Tat could potentially activate the transcription machinery during initiation, elongation, or both. We used an immobilized HIV-1 promoter template with a reversible lac repressor (LacR) elongation block inserted downstream to dissect the stages in transcription affected by Tat. Transcription complexes assembled in the absence of Tat and blocked by LacR cannot be activated by incubation with Tat alone. These complexes can, however, be activated if Tat is added in combination with cellular factors. In this system, Tat also promoted the assembly of preinitiation complexes capable of elongating efficiently, suggesting that Tat can associate with transcription complex at an early stage. These data indicate that Tat can activate elongation of RNA polymerase by modifying an already elongating transcription complex. The data also suggest the possibility that Tat can interact with initiation complexes.
Asunto(s)
Regulación Viral de la Expresión Génica , Productos del Gen tat/metabolismo , VIH-1/genética , Extensión de la Cadena Peptídica de Translación , ARN Polimerasa II/genética , Células HeLa , Humanos , Moldes Genéticos , Transcripción Genética , Productos del Gen tat del Virus de la Inmunodeficiencia HumanaRESUMEN
Splicing of pre-mRNAs involves two sequential transesterification reactions commonly referred to as the first and second steps. In Saccharomyces cerevisiae, four proteins, Prp16p, Prp17p, Prp18p, and Slu7p are exclusively required for the second step of splicing. The human homologs of Prp16p, Prp17p, and Prp18p have been identified, and the human proteins hPrp16 and hPrp18 have been shown to be required for the second step of splicing in vitro. Here we provide further evidence for the functional conservation of the second step factors between yeast and humans. Human hPrp17, which is 35% identical to the S. cerevisiae protein, is able to partially rescue the temperature-sensitive phenotype in a yeast strain where PRP17 has been knocked out, suggesting that the human and yeast proteins are functionally conserved. Overexpression of hPrp17 in the knockout yeast strain partially rescues the splicing defect seen in vitro and in vivo. In HeLa cells, hPrp17 is highly concentrated in the nuclear speckles, as is SC35 and many other splicing factors, thus providing further support that this protein also functions as a splicing factor in humans.