RESUMEN
The ribosome is an essential organelle in charge of the translational processes in all kinds of cells. Currently, the scenario of its function has been significantly expanded from the classic machine for protein synthesis to a regulatory platform for quality control to maintain the protein homeostasis in a living cell. The ribosome is much more than a mechanical device with a static structure: it is inherently dynamic in structure and function, especially in response to the environmental fluctuations. Considerable effort has been made to regulate its structure and physiological function by engineering the components of a ribosome. The findings of the pioneering studies significantly deepened our understanding of a ribosome and exemplified how a ribosome could be engineered for biotechnology purposes in the era of synthetic biology. The engineering of ribosome offered highly accessible methods capable of comprehensively optimizing the performance of strains of industrial importance. In this article, the relevant recent advances were systematically reviewed.
Asunto(s)
Aminoácidos/química , Biotecnología/métodos , Biosíntesis de Proteínas , Ribosomas/química , Ribosomas/enzimología , Biología Sintética/métodos , Aminoácidos/síntesis química , Aminoácidos/metabolismo , Codón sin Sentido/química , Codón sin Sentido/genética , Farmacorresistencia Bacteriana/genética , Ingeniería Metabólica/métodos , Ingeniería de Proteínas/métodos , ARN Catalítico/biosíntesis , ARN Catalítico/química , ARN Catalítico/genética , ARN Ribosómico/química , ARN de Transferencia/química , ARN de Transferencia/genética , Ribosomas/metabolismoRESUMEN
Nonsense-mediated decay (NMD) is a surveillance system that degrades mRNAs containing a premature termination codon (PTC) and plays important roles in protein homeostasis and disease. The efficiency of NMD is variable, impacting the clinical outcome of genetic mutations. However, limited resolution of bulk analyses has hampered the study of NMD efficiency. Here, we develop an assay to visualize NMD of individual mRNA molecules in real time. We find that NMD occurs with equal probability during each round of translation of an mRNA molecule. However, this probability is variable and depends on the exon sequence downstream of the PTC, the PTC-to-intron distance, and the number of introns both upstream and downstream of the PTC. Additionally, a subpopulation of mRNAs can escape NMD, further contributing to variation in NMD efficiency. Our study uncovers real-time dynamics of NMD, reveals key mechanisms that influence NMD efficiency, and provides a powerful method to study NMD.
Asunto(s)
Codón sin Sentido/genética , Degradación de ARNm Mediada por Codón sin Sentido/genética , ARN Mensajero/genética , Codón sin Sentido/química , Exones/genética , Humanos , Intrones/genética , Mutación/genética , Estabilidad del ARN/genética , ARN Mensajero/química , Imagen Individual de MoléculaRESUMEN
Classical genetic studies in European rabbits (Oryctolagus cuniculus) suggested the presence of two alleles at the brown coat colour locus: a wild-type B allele that gives dense black pigment throughout the coat and a recessive b allele that in the homozygous condition (b/b genotype) produces brown rabbits that are unable to develop black pigmentation. In several other species, this locus is determined by mutations in the tyrosinase-related protein 1 (TYRP1) gene, encoding a melanocyte enzyme needed for the production of dark eumelanin. In this study, we investigated the rabbit TYRP1 gene as a strong candidate for the rabbit brown coat colour locus. A total of 3846 bp of the TYRP1 gene were sequenced in eight rabbits of different breeds and identified 23 single nucleotide polymorphisms (SNPs; 12 in intronic regions, five in exons and six in the 3'-untranslated region) and an insertion/deletion of 13 bp, in the 3'-untranslated region, organised in a few haplotypes. A mutation in exon 2 (g.41360196G>A) leads to a premature stop codon at position 190 of the deduced amino acid sequence (p.Trp190ter). Therefore, translation predicts a truncated TYRP1 protein lacking almost completely the tyrosinase domain. Genotyping 203 rabbits of 32 different breeds identified this mutation only in brown Havana rabbits. Its potential functional relevance in disrupting the TYRP1 protein and its presence only in brown animals strongly argue for this non-sense mutation being a causative mutation for the recessive b allele at the brown locus in Oryctolagus cuniculus.
Asunto(s)
Oxidorreductasas/genética , Pigmentación , Conejos/fisiología , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Codón sin Sentido/química , Codón sin Sentido/genética , Codón sin Sentido/metabolismo , Codón de Terminación/química , Codón de Terminación/genética , Codón de Terminación/metabolismo , Oxidorreductasas/química , Oxidorreductasas/metabolismo , Reacción en Cadena de la Polimerasa/veterinaria , Polimorfismo de Longitud del Fragmento de Restricción , Polimorfismo de Nucleótido Simple , Conejos/genética , Especificidad de la EspecieRESUMEN
Maple Syrup Urine Disease is a rare metabolic disorder caused by reduced/absent activity of the branched chain α-Ketoacid dehydrogenase enzyme complex. Mutations in BCKDHA, BCKDHB, and DBT, that encode important subunits of the enzyme complex namely E1α, E1ß, and E2, are the primary cause for the disease. We have performed the first molecular genetic analysis of MSUD from India on nine patients exhibiting classical MSUD symptoms. BCKDHA and BCKDHB mutations were identified in four and five patients, respectively including seven novel mutations namely the BCKDHA c.1249delC, c.1312T>C, and c.1561T>A and the BCKDHB c.401T>A, c.548G>A, c.964A>G, and c.1065delT. The BCKDHB c.970C>T (p.R324X) mutation was shown to trigger nonsense mediated decay-based degradation of the transcript. Seven of the total 11 mutations resulted in perturbations in the E1α or E1ß C-termini either through altered termination or through an amino acid change; these are expected to result in disruption of E1 enzyme complex assembly. Our study has therefore revealed that BCKDHA and BCKDHB mutations might be primarily responsible for MSUD in the Indian population.
Asunto(s)
3-Metil-2-Oxobutanoato Deshidrogenasa (Lipoamida)/química , Enfermedad de la Orina de Jarabe de Arce/genética , Complejos Multienzimáticos/química , Mutación Missense , Regiones no Traducidas 3' , 3-Metil-2-Oxobutanoato Deshidrogenasa (Lipoamida)/genética , Secuencia de Aminoácidos , Aminoácidos/química , Secuencia de Bases , Codón sin Sentido/química , Codón sin Sentido/genética , Análisis Mutacional de ADN , Femenino , Pruebas Genéticas , Genoma Humano , Genotipo , Humanos , India , Lactante , Recién Nacido , Masculino , Enfermedad de la Orina de Jarabe de Arce/diagnóstico , Datos de Secuencia Molecular , Complejos Multienzimáticos/genética , Estabilidad del ARN , Alineación de Secuencia , Análisis de Secuencia de Proteína , Eliminación de SecuenciaRESUMEN
A stop or nonsense codon is an in-frame triplet within a messenger RNA that signals the termination of translation. One common feature shared among all three nonsense codons (UAA, UAG, and UGA) is a uridine present at the first codon position. It has been recently shown that the conversion of this uridine into pseudouridine (Ψ) suppresses translation termination, both in vitro and in vivo. Furthermore, decoding of the pseudouridylated nonsense codons is accompanied by the incorporation of two specific amino acids in a nonsense codon-dependent fashion. Ψ differs from uridine by a single N¹H group at the C5 position; how Ψ suppresses termination and, more importantly, enables selective decoding is poorly understood. Here, we provide molecular rationales for how pseudouridylated stop codons are selectively decoded. Our analysis applies crystal structures of ribosomes in varying states of translation to consider weakened interaction of Ψ with release factor; thermodynamic and geometric considerations of the codon-anticodon base pairs to rank and to eliminate mRNA-tRNA pairs; the mechanism of fidelity check of the codon-anticodon pairing by the ribosome to evaluate noncanonical codon-anticodon base pairs and the role of water. We also consider certain tRNA modifications that interfere with the Ψ-coordinated water in the major groove of the codon-anticodon mini-helix. Our analysis of nonsense codons enables prediction of potential decoding properties for Ψ-modified sense codons, such as decoding ΨUU potentially as Cys and Tyr. Our results provide molecular rationale for the remarkable dynamics of ribosome decoding and insights on possible reprogramming of the genetic code using mRNA modifications.
Asunto(s)
Codón sin Sentido/química , Codón/química , Seudouridina/química , Modelos Moleculares , Biosíntesis de Proteínas/genética , ARN Mensajero/química , ARN Ribosómico/química , ARN de Transferencia/químicaRESUMEN
A structure-activity relationship (SAR) study was carried out to identify novel, small molecular weight compounds which induce readthrough of premature termination codons. In particular, analogs of RTC13, 1, were evaluated. In addition, hypothesizing that these compounds exhibit their activity by binding to the ribosome, we prepared the hybrid analogs 13 containing pyrimidine bases and these also showed good readthrough activity.
Asunto(s)
Ataxia Telangiectasia/genética , Proteínas de Ciclo Celular/metabolismo , Codón sin Sentido/metabolismo , Proteínas de Unión al ADN/metabolismo , Evaluación Preclínica de Medicamentos , Furanos/síntesis química , Furanos/farmacología , Proteínas Serina-Treonina Quinasas/metabolismo , Tiazoles/síntesis química , Tiazoles/farmacología , Proteínas Supresoras de Tumor/metabolismo , Ataxia Telangiectasia/tratamiento farmacológico , Ataxia Telangiectasia/metabolismo , Proteínas de la Ataxia Telangiectasia Mutada , Proteínas de Ciclo Celular/biosíntesis , Proteínas de Ciclo Celular/genética , Línea Celular , Codón sin Sentido/química , Codón sin Sentido/genética , Codón de Terminación/genética , Codón de Terminación/metabolismo , Proteínas de Unión al ADN/biosíntesis , Proteínas de Unión al ADN/genética , Diseño de Fármacos , Furanos/química , Ensayos Analíticos de Alto Rendimiento , Estructura Molecular , Terapia Molecular Dirigida , Mutación , Sistemas de Lectura Abierta , Terminación de la Cadena Péptídica Traduccional/genética , Biosíntesis de Proteínas/genética , Proteínas Serina-Treonina Quinasas/biosíntesis , Proteínas Serina-Treonina Quinasas/genética , ARN Mensajero/metabolismo , Ribosomas/metabolismo , Relación Estructura-Actividad , Tiazoles/química , Activación Transcripcional , Proteínas Supresoras de Tumor/biosíntesis , Proteínas Supresoras de Tumor/genéticaAsunto(s)
ARN Mensajero/genética , Animales , Codón sin Sentido/química , Codón sin Sentido/genética , Exosomas/genética , Hongos/genética , Humanos , Mamíferos , Modelos Moleculares , Conformación Proteica , Subunidades de Proteína/genética , ARN Mensajero/química , Telomerasa/química , Telomerasa/genéticaRESUMEN
The ability to incorporate chemical probes into peptides is of great importance because it can render novel functionality to proteins and greatly expand our capacity to investigate complex biological systems. A methodology developed by the Schultz laboratory provides a unique strategy to incorporate chemical probes as unnatural amino acids into proteins by "expanding the genetic code" of the host cell. A recent application of this methodology that allows the site-specific incorporation of three NMR-active probes into proteins demonstrates the potential for researchers to explore avenues that are not easily achievable with existing methods.
Asunto(s)
Aminoácidos/química , Ácido Graso Sintasas/química , Mutagénesis Sitio-Dirigida , Resonancia Magnética Nuclear Biomolecular , Aminoacil-ARNt Sintetasas/química , Aminoacil-ARNt Sintetasas/metabolismo , Isótopos de Carbono , Codón sin Sentido/química , Ácido Graso Sintasas/genética , Flúor , Isótopos de Nitrógeno , Fenilalanina/análogos & derivados , Fenilalanina/química , Tirosina/análogos & derivados , Tirosina/químicaRESUMEN
Premature stop codons in CACNA1A, which encodes the alpha(1A) subunit of neuronal P/Q-type (Ca(V)2.1) Ca(2+) channels, cause episodic ataxia type 2 (EA2). CACNA1A undergoes extensive alternative splicing, which contributes to the pharmacological and kinetic heterogeneity of Ca(V)2.1-mediated Ca(2+) currents. We identified three novel heterozygous stop codon mutations associated with EA2 in an alternately spliced exon (37A), which encodes part of an EF-hand motif required for Ca(2+)-dependent facilitation. One family had a C to G transversion (Y1854X). A dinucleotide deletion results in the same premature stop codon in a second family, and a further single nucleotide change leads to a different truncation (R1858X) in a de novo case of EA2. Expression studies of the Y1854X mutation revealed loss of Ca(V)2.1-mediated current. Because these mutations do not affect the alternate exon 37B, these findings reveal unexpected dependence of cerebellar function on intact exon 37A-containing Ca(V)2.1 channels.
Asunto(s)
Empalme Alternativo/genética , Canales de Calcio Tipo N/genética , Codón sin Sentido/genética , Motivos EF Hand/genética , Mutación del Sistema de Lectura/genética , Isoformas de Proteínas/genética , Ataxias Espinocerebelosas/genética , Adulto , Animales , Cerebelo/química , Cerebelo/fisiopatología , Codón sin Sentido/química , Exones/genética , Femenino , Variación Genética/genética , Humanos , Masculino , Linaje , Isoformas de Proteínas/química , Ataxias Espinocerebelosas/diagnóstico , Ataxias Espinocerebelosas/fisiopatología , Xenopus laevisRESUMEN
DNA polymerase iota (Pol iota) of mammals is a member of the Y family of DNA polymerases. Among many other genome caretakers, these enzymes are responsible for maintaining genome stability. The members of the Y-family DNA polymerases take part in translesion DNA synthesis, bypassing some DNA lesions, and are characterized by low fidelity of DNA synthesis. A unique ability of Pol iota to predominantly incorporate G opposite T allowed us to identify the product of this enzyme among those synthesized by other DNA polymerases. This product can be called a "false note" of Pol iota. We measured the enzyme activity of Pol iota in crude extracts of cells from different organs of five inbred strains of mice (N3H/Sn, 101/H, C57BL/6, BALB/c, 129/J) that differed in a number of parameters. The "false note" of Pol iota was clearly sounding only in the extracts of testis and brain cells from four analyzed strains: N3H/Sn, 101/H, C57BL/6, BALB/c. In mice of 129/J strain that had a nonsense mutation in the second exon of the pol iota gene, the Pol iota activity was reliably detectable only in the extracts of brain. The data show that the active enzyme can be formed in some cell types even if they carry a nonsense mutation in the pol iota gene. This supports tissue-specific regulation of pol iota gene expression through alternative splicing. A semiquantitative determination of pol iota activity in mice strains different in their radiosensitivity suggests a reciprocal correlation between the enzyme activity of pol iota in testis and the resistance of mice to radiation.
Asunto(s)
Codón sin Sentido/química , Codón sin Sentido/metabolismo , ADN Polimerasa Dirigida por ADN/química , ADN Polimerasa Dirigida por ADN/genética , Inestabilidad Genómica , Animales , Encéfalo/enzimología , Dominio Catalítico , Replicación del ADN/genética , ADN Polimerasa Dirigida por ADN/metabolismo , Guanina/metabolismo , Masculino , Ratones , Ratones Endogámicos BALB C , Ratones Endogámicos C3H , Ratones Endogámicos C57BL , Inhibidores de la Síntesis del Ácido Nucleico , Especificidad de Órganos/genética , Testículo/enzimología , Testículo/efectos de la radiación , Timina/metabolismo , ADN Polimerasa iotaRESUMEN
An estimated one third of all inherited genetic disorders and many forms of cancer are caused by premature (nonsense) termination codons. Aminoglycoside antibiotics are candidate drugs for a large number of such genetic diseases; however, aminoglycosides are toxic, lack specificity and show low efficacy in this application. Because translational termination is an active process, we considered that steric hindrance by antisense sequences could trigger the ribosome's "default mode" of readthrough when positioned near nonsense codons. To test this hypothesis, we performed experiments using plasmids containing a luciferase reporter with amber, ochre and opal nonsense mutations within the luxB gene in Escherichia coli. The nonspecific termination inhibitors gentamicin and paromomycin and six antisense peptide nucleic acids (PNA) spanning the termination region were tested for their potential to suppress the luxB mutation. Gentamicin and paromomycin increased luciferase activity up to 2.5- and 10-fold, respectively. Two of the PNAs increased Lux activity up to 2.5-fold over control levels, with no significant effect on cell growth or mRNA levels. Thus, it is possible to significantly suppress nonsense mutations within target genes using antisense PNAs. The mechanism of suppression likely involves enhanced readthrough, but this requires further investigation. Nonsense termination in human cells may also be susceptible to suppression by antisense agents, providing a new approach to address numerous diseases caused by nonsense mutations.
Asunto(s)
Codón sin Sentido , Escherichia coli/genética , Genes Bacterianos , Genes Supresores , Mutación , Antibacterianos/farmacología , Codón sin Sentido/química , Codón sin Sentido/efectos de los fármacos , Codón sin Sentido/genética , Relación Dosis-Respuesta a Droga , Escherichia coli/crecimiento & desarrollo , Genes Bacterianos/efectos de los fármacos , Genes Bacterianos/genética , Genes Reporteros , Genes Supresores/efectos de los fármacos , Gentamicinas/farmacología , Luciferasas/análisis , Luciferasas/genética , Mutación/efectos de los fármacos , Mutación/genética , Paromomicina/farmacología , Plásmidos , ARN Mensajero/análisis , ARN Mensajero/efectos de los fármacos , ARN Mensajero/metabolismoRESUMEN
Chemical diversity of protein molecules can be expanded through in vitro incorporation of unnatural amino acids in response to a nonsense codon. Chemically misacylated tRNAs are used for tethering unnatural amino acids to a nonsense-mutated target codon (nonsense suppression). In the course of experiments to introduce S-(2-nitrobenzyl)cysteine (NBC) into a targeted location of human erythropoietin, we found that NBC incorporates more efficiently at lower temperatures. In addition, at a fixed reaction temperature, more NBC was incorporated with a reduced supply of ATP. Since the rate of peptide elongation was remarkably higher at the elevated temperature or with enhanced supply of ATP, these results indicate that the efficiency of nonsense suppression is inversely correlated to the peptide elongation rate. Therefore, maximal yield of nonsense-suppressed proteins is obtained at a compromised elongation rate. The present result will offer a primary guideline to optimize the reaction conditions for in vitro production of protein molecules containing unnatural amino acids.
Asunto(s)
Anticodón/química , Codón sin Sentido/química , Cisteína/química , Eritropoyetina/biosíntesis , Calor , Biosíntesis de Proteínas , Secuencia de Bases , Sistema Libre de Células/química , Cisteína/análogos & derivados , Escherichia coli/química , Humanos , Datos de Secuencia MolecularRESUMEN
It has been reported that eukaryotic organisms have a nonsense-mediated mRNA decay (NMD) system to exclude aberrant mRNAs that produce truncated proteins. NMD is an RNA surveillance pathway that degrades mRNAs possessing premature translation termination codons (PTCs), thus avoiding production of possibly toxic truncated proteins. Three interacting proteins, UPF1, UPF2 and UPF3, are required for NMD in mammals and yeasts, and their amino acid sequences are well conserved among most eukaryotes, including plants. In this study, 'The Arabidopsis Information Resource' database was searched for mRNAs with premature termination codons. We selected five of these mRNAs and checked for the presence of PTCs in these mRNAs when translated in vivo. As a result we identified aberrant mRNAs produced by alternative splicing for each gene. These genes produced at least one alternative splicing variant including a PTC (PTC+) and another variant without a PTC (PTC-). We analyzed their PTC+/PTC- ratios in wild-type Arabidopsis and upf3 mutant plants and showed that the PTC+/PTC- ratios were higher in atupf3 mutant plants than wild-type plants and that the atupf3 mutant was less able to degrade mRNAs with premature termination codons than wild-type plants. This indicated that the AtUPF3 gene is required by the plant NMD system to obviate aberrantly spliced mRNA.
Asunto(s)
Proteínas de Arabidopsis/fisiología , Arabidopsis/fisiología , Codón sin Sentido/fisiología , ARN Mensajero/metabolismo , ARN de Planta/metabolismo , Empalme Alternativo/fisiología , Codón sin Sentido/química , Regulación de la Expresión Génica de las Plantas , Filogenia , Procesamiento Postranscripcional del ARN , Estabilidad del ARNRESUMEN
Caged compounds have covalently attached groups that are rapidly cleaved upon exposure to UV light. Attachment of photolabile groups makes the molecule inert until photolysis releases it in its bioactive form. When caged compounds are applied to the experimental system in advance, the concentration jump of biologically active substances can be brought about immediately in a limited area upon irradiation with pulsed and focused UV light. Therefore, caged compounds of low molecular weight, which are commercially available, have been used effectively to study the mechanisms of temporal biological phenomena, such as muscle contraction, intracellular signaling, and neurotransmission. Because many proteins and peptides play important roles in these phenomena, their caged derivatives should serve as powerful tools to clarify complex biological systems. To prepare caged proteins and peptides, several groups have improved upon a chemical modification method, as well as developed two new methods: (1) nonsense codon suppression and (2) solid-phase peptide synthesis. In this review, we summarize recent advances made in the design, preparation, and application of caged peptides and proteins.