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1.
Commun Biol ; 6(1): 962, 2023 09 21.
Artigo em Inglês | MEDLINE | ID: mdl-37735514

RESUMO

BRAF mutations occur early in serrated colorectal cancers, but their long-term influence on tissue homeostasis is poorly characterized. We investigated the impact of short-term (3 days) and long-term (6 months) expression of BrafV600E in the intestinal tissue of an inducible mouse model. We show that BrafV600E perturbs the homeostasis of intestinal epithelial cells, with impaired differentiation of enterocytes emerging after prolonged expression of the oncogene. Moreover, BrafV600E leads to a persistent transcriptional reprogramming with enrichment of numerous gene signatures indicative of proliferation and tumorigenesis, and signatures suggestive of metabolic rewiring. We focused on the top-ranking cholesterol biosynthesis signature and confirmed its increased expression in human serrated lesions. Functionally, the cholesterol lowering drug atorvastatin prevents the establishment of intestinal crypt hyperplasia in BrafV600E-mutant mice. Overall, our work unveils the long-term impact of BrafV600E expression in intestinal tissue and suggests that colorectal cancers with mutations in BRAF might be prevented by statins.


Assuntos
Neoplasias Colorretais , Proteínas Proto-Oncogênicas B-raf , Animais , Humanos , Camundongos , Colesterol , Neoplasias Colorretais/genética , Metabolismo dos Lipídeos , Proteínas Proto-Oncogênicas B-raf/genética , Ativação Transcricional
2.
Nat Commun ; 13(1): 3644, 2022 06 25.
Artigo em Inglês | MEDLINE | ID: mdl-35752733

RESUMO

FANCM suppresses crossovers in plants by unwinding recombination intermediates. In wheat, crossovers are skewed toward the chromosome ends, thus limiting generation of novel allelic combinations. Here, we observe that FANCM maintains the obligate crossover in tetraploid and hexaploid wheat, thus ensuring that every chromosome pair exhibits at least one crossover, by localizing class I crossover protein HEI10 at pachytene. FANCM also suppresses class II crossovers that increased 2.6-fold in fancm msh5 quadruple mutants. These data are consistent with a role for FANCM in second-end capture of class I designated crossover sites, whilst FANCM is also required to promote formation of non-crossovers. In hexaploid wheat, genetic mapping reveals that crossovers increase by 31% in fancm compared to wild type, indicating that fancm could be an effective tool to accelerate breeding. Crossover rate differences in fancm correlate with wild type crossover distributions, suggesting that chromatin may influence the recombination landscape in similar ways in both wild type and fancm.


Assuntos
Troca Genética , Triticum , Meiose/genética , Melhoramento Vegetal , Triticum/genética
3.
PLoS One ; 17(2): e0262364, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35130302

RESUMO

Research into the metabolism of the non-essential amino acid (NEAA) proline in cancer has gained traction in recent years. The last step in the proline biosynthesis pathway is catalyzed by pyrroline-5-carboxylate reductase (PYCR) enzymes. There are three PYCR enzymes: mitochondrial PYCR1 and 2 and cytosolic PYCR3 encoded by separate genes. The expression of the PYCR1 gene is increased in numerous malignancies and correlates with poor prognosis. PYCR1 expression sustains cancer cells' proliferation and survival and several mechanisms have been implicated to explain its oncogenic role. It has been suggested that the biosynthesis of proline is key to sustain protein synthesis, support mitochondrial function and nucleotide biosynthesis. However, the links between proline metabolism and cancer remain ill-defined and are likely to be tissue specific. Here we use a combination of human dataset, human tissue and mouse models to show that the expression levels of the proline biosynthesis enzymes are significantly increased during colorectal tumorigenesis. Functionally, the expression of mitochondrial PYCRs is necessary for cancer cells' survival and proliferation. However, the phenotypic consequences of PYCRs depletion could not be rescued by external supplementation with either proline or nucleotides. Overall, our data suggest that, despite the mechanisms underlying the role of proline metabolism in colorectal tumorigenesis remain elusive, targeting the proline biosynthesis pathway is a suitable approach for the development of novel anti-cancer therapies.


Assuntos
Neoplasias Colorretais
4.
Cell Death Discov ; 6: 104, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-33083024

RESUMO

The metabolism of the non-essential amino acid L-proline is emerging as a key pathway in the metabolic rewiring that sustains cancer cells proliferation, survival and metastatic spread. Pyrroline-5-carboxylate reductase (PYCR) and proline dehydrogenase (PRODH) enzymes, which catalyze the last step in proline biosynthesis and the first step of its catabolism, respectively, have been extensively associated with the progression of several malignancies, and have been exposed as potential targets for anticancer drug development. As investigations into the links between proline metabolism and cancer accumulate, the complexity, and sometimes contradictory nature of this interaction emerge. It is clear that the role of proline metabolism enzymes in cancer depends on tumor type, with different cancers and cancer-related phenotypes displaying different dependencies on these enzymes. Unexpectedly, the outcome of rewiring proline metabolism also differs between conditions of nutrient and oxygen limitation. Here, we provide a comprehensive review of proline metabolism in cancer; we collate the experimental evidence that links proline metabolism with the different aspects of cancer progression and critically discuss the potential mechanisms involved.

5.
Dalton Trans ; 45(16): 7104-13, 2016 Apr 28.
Artigo em Inglês | MEDLINE | ID: mdl-27008377

RESUMO

Vanadium complexes have been previously utilised as potent inhibitors of cysteine based phosphatases (CBPs). Herein, we present the synthesis and characterisation of two new fluorescently labelled vanadyl complexes (14 and 15) with bridged di-picolinic acid ligands. These compounds differ significantly from previous vanadyl complexes with phosphatase inhibition properties in that the metal-chelating part is a single tetradentate unit, which should afford greater stability and scope for synthetic elaboration than the earlier complexes. These new complexes inhibit a selection of cysteine based phosphatases (CBPs) in the nM range with some selectivity. Fluorescence spectroscopic studies (including fluorescence anisotropy) were carried out to demonstrate that the complexes are not simply acting as vanadyl delivery vehicles but they interact with the proteins. Finally, we present preliminary fluorescence microscopy studies to demonstrate that the complexes are cell permeable and localise throughout the cytoplasm of NIH3T3 cells.


Assuntos
Compostos de Dansil/química , Compostos Organometálicos/síntese química , Compostos Organometálicos/farmacologia , Monoéster Fosfórico Hidrolases/antagonistas & inibidores , Ácidos Picolínicos/química , Vanadatos/química , Animais , Transporte Biológico , Técnicas de Química Sintética , Inibidores Enzimáticos/síntese química , Inibidores Enzimáticos/química , Inibidores Enzimáticos/metabolismo , Inibidores Enzimáticos/farmacologia , Concentração Inibidora 50 , Ligantes , Camundongos , Células NIH 3T3 , Compostos Organometálicos/química , Compostos Organometálicos/metabolismo , Permeabilidade
6.
Science ; 327(5963): 328-31, 2010 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-20075252

RESUMO

Artemisinin is a plant natural product produced by Artemisia annua and the active ingredient in the most effective treatment for malaria. Efforts to eradicate malaria are increasing demand for an affordable, high-quality, robust supply of artemisinin. We performed deep sequencing on the transcriptome of A. annua to identify genes and markers for fast-track breeding. Extensive genetic variation enabled us to build a detailed genetic map with nine linkage groups. Replicated field trials resulted in a quantitative trait loci (QTL) map that accounts for a significant amount of the variation in key traits controlling artemisinin yield. Enrichment for positive QTLs in parents of new high-yielding hybrids confirms that the knowledge and tools to convert A. annua into a robust crop are now available.


Assuntos
Antimaláricos/metabolismo , Artemisia/genética , Artemisia/metabolismo , Artemisininas/metabolismo , Mapeamento Cromossômico , Genes de Plantas , Locos de Características Quantitativas , Cruzamentos Genéticos , DNA Complementar , Perfilação da Expressão Gênica , Estudos de Associação Genética , Humanos , Malária/tratamento farmacológico , Mutação , Fenótipo , Polimorfismo de Nucleotídeo Único , Análise de Sequência de DNA
7.
Plant Mol Biol ; 60(4): 555-63, 2006 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-16525891

RESUMO

Esters are important contributors to the aroma of numerous flowers and fruits. Acetate esters such as geranyl acetate, phenylethyl acetate and benzyl acetate are generated as a result of the action of alcohol acetyltransferases (AATs). Numerous homologous AATs from various plants have been characterized using in-vitro assays. To study the function of rose alcohol acetyltransferase (RhAAT) in planta, we generated transgenic petunia plants expressing the rose gene under the control of a CaMV-35S promoter. Although the preferred substrate of RhAAT in vitro is geraniol, in transgenic petunia flowers, it used phenylethyl alcohol and benzyl alcohol to produce the corresponding acetate esters, not generated by control flowers. The level of benzyl alcohol emitted by the flowers of different transgenic lines was ca. three times higher than that of phenylethyl alcohol, which corresponded to the ratio between the respective products, i.e. ca. three times more benzyl acetate than phenylethyl acetate. Feeding of transgenic petunia tissues with geraniol or octanol led to the production of their respective acetates, suggesting the dependence of volatile production on substrate availability.


Assuntos
Acetatos/metabolismo , Compostos de Benzil/metabolismo , Flores/metabolismo , Petunia/metabolismo , Álcool Feniletílico/análogos & derivados , Propanóis/metabolismo , Proteínas/metabolismo , Rosa/enzimologia , Acetatos/análise , Acetatos/química , Monoterpenos Acíclicos , Álcool Benzílico/análise , Álcool Benzílico/química , Cromatografia Gasosa , Flores/genética , Cinética , Espectrometria de Massas , Petunia/genética , Álcool Feniletílico/análise , Álcool Feniletílico/química , Álcool Feniletílico/metabolismo , Folhas de Planta/metabolismo , Plantas Geneticamente Modificadas , Proteínas/genética , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Rosa/genética , Especificidade por Substrato , Terpenos/análise , Terpenos/química , Volatilização
8.
Planta ; 222(1): 37-46, 2005 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-15883834

RESUMO

Flowering is a unique and highly programmed process, but hardly anything is known about the developmentally regulated proteome changes in petals. Here, we employed proteomic technologies to study petal development in rose (Rosa hybrida). Using two-dimensional polyacrylamide gel electrophoresis, we generated stage-specific (closed bud, mature flower and flower at anthesis) petal protein maps with ca. 1,000 unique protein spots. Expression analyses of all resolved protein spots revealed that almost 30% of them were stage-specific, with ca. 90 protein spots for each stage. Most of the proteins exhibited differential expression during petal development, whereas only ca. 6% were constitutively expressed. Eighty-two of the resolved proteins were identified by mass spectrometry and annotated. Classification of the annotated proteins into functional groups revealed energy, cell rescue, unknown function (including novel sequences) and metabolism to be the largest classes, together comprising ca. 90% of all identified proteins. Interestingly, a large number of stress-related proteins were identified in developing petals. Analyses of the expression patterns of annotated proteins and their corresponding RNAs confirmed the importance of proteome characterization.


Assuntos
Flores/crescimento & desenvolvimento , Flores/metabolismo , Regulação da Expressão Gênica de Plantas , Proteínas de Plantas/metabolismo , Proteoma/metabolismo , Rosa/crescimento & desenvolvimento , Rosa/metabolismo , Perfilação da Expressão Gênica , Regulação da Expressão Gênica no Desenvolvimento
9.
Plant Physiol ; 131(4): 1868-76, 2003 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-12692346

RESUMO

The aroma of roses (Rosa hybrida) is due to more than 400 volatile compounds including terpenes, esters, and phenolic derivatives. 2-Phenylethyl acetate, cis-3-hexenyl acetate, geranyl acetate, and citronellyl acetate were identified as the main volatile esters emitted by the flowers of the scented rose var. "Fragrant Cloud." Cell-free extracts of petals acetylated several alcohols, utilizing acetyl-coenzyme A, to produce the corresponding acetate esters. Screening for genes similar to known plant alcohol acetyltransferases in a rose expressed sequence tag database yielded a cDNA (RhAAT1) encoding a protein with high similarity to several members of the BAHD family of acyltransferases. This cDNA was functionally expressed in Escherichia coli, and its gene product displayed acetyl-coenzyme A:geraniol acetyltransferase enzymatic activity in vitro. The RhAAT1 protein accepted other alcohols such as citronellol and 1-octanol as substrates, but 2-phenylethyl alcohol and cis-3-hexen-1-ol were poor substrates, suggesting that additional acetyltransferases are present in rose petals. The RhAAT1 protein is a polypeptide of 458 amino acids, with a calculated molecular mass of 51.8 kD, pI of 5.45, and is active as a monomer. The RhAAT1 gene was expressed exclusively in floral tissue with maximum transcript levels occurring at stage 4 of flower development, where scent emission is at its peak.


Assuntos
Acetiltransferases/metabolismo , Ésteres/metabolismo , Monoterpenos/metabolismo , Óleos Voláteis/metabolismo , Rosa/enzimologia , Rosa/crescimento & desenvolvimento , Terpenos/metabolismo , Acetiltransferases/genética , Acetiltransferases/isolamento & purificação , Monoterpenos Acíclicos , Sequência de Aminoácidos , Flores/enzimologia , Flores/genética , Flores/crescimento & desenvolvimento , Flores/metabolismo , Regulação Enzimológica da Expressão Gênica , Regulação da Expressão Gênica de Plantas , Cinética , Dados de Sequência Molecular , Estrutura Molecular , Odorantes , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Rosa/genética , Rosa/metabolismo , Homologia de Sequência , Especificidade por Substrato
10.
Plant Cell ; 14(10): 2325-38, 2002 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-12368489

RESUMO

For centuries, rose has been the most important crop in the floriculture industry; its economic importance also lies in the use of its petals as a source of natural fragrances. Here, we used genomics approaches to identify novel scent-related genes, using rose flowers from tetraploid scented and nonscented cultivars. An annotated petal EST database of approximately 2100 unique genes from both cultivars was created, and DNA chips were prepared and used for expression analyses of selected clones. Detailed chemical analysis of volatile composition in the two cultivars, together with the identification of secondary metabolism-related genes whose expression coincides with scent production, led to the discovery of several novel flower scent-related candidate genes. The function of some of these genes, including a germacrene D synthase, was biochemically determined using an Escherichia coli expression system. This work demonstrates the advantages of using the high-throughput approaches of genomics to detail traits of interest expressed in a cultivar-specific manner in nonmodel plants. EST sequences were submitted to the GenBank database (accession numbers BQ 103855 to BQ 106728).


Assuntos
Alquil e Aril Transferases/genética , Flores/genética , Perfumes/metabolismo , Rosa/genética , Sesquiterpenos de Germacrano , Alquil e Aril Transferases/metabolismo , Sequência de Aminoácidos , Clonagem Molecular , DNA Complementar/química , DNA Complementar/genética , Escherichia coli/genética , Etiquetas de Sequências Expressas , Flores/química , Flores/crescimento & desenvolvimento , Cromatografia Gasosa-Espectrometria de Massas , Regulação da Expressão Gênica no Desenvolvimento , Regulação da Expressão Gênica de Plantas , Metiltransferases/genética , Metiltransferases/metabolismo , Dados de Sequência Molecular , Análise de Sequência com Séries de Oligonucleotídeos , Perfumes/química , Fenótipo , Rosa/química , Rosa/crescimento & desenvolvimento , Análise de Sequência de DNA , Homologia de Sequência de Aminoácidos , Sesquiterpenos/química , Sesquiterpenos/metabolismo
11.
Plant Physiol ; 129(4): 1899-907, 2002 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12177504

RESUMO

Rose (Rosa hybrida) flowers produce and emit a diverse array of volatiles, characteristic to their unique scent. One of the most prominent compounds in the floral volatiles of many rose varieties is the methoxylated phenolic derivative 3,5-dimethoxytoluene (orcinol dimethyl ether). Cell-free extracts derived from developing rose petals displayed O-methyltransferase (OMT) activities toward several phenolic substrates, including 3,5-dihydroxytoluene (orcinol), 3-methoxy,5-hydroxytoluene (orcinol monomethyl ether), 1-methoxy, 2-hydroxy benezene (guaiacol), and eugenol. The activity was most prominent in rose cv Golden Gate, a variety that produces relatively high levels of orcinol dimethyl ether, as compared with rose cv Fragrant Cloud, an otherwise scented variety but which emits almost no orcinol dimethyl ether. Using a functional genomics approach, we have identified and characterized two closely related cDNAs from a rose petal library that each encode a protein capable of methylating the penultimate and immediate precursors (orcinol and orcinol monomethyl ether, respectively) to give the final orcinol dimethyl ether product. The enzymes, designated orcinol OMTs (OOMT1 and OOMT2), are closely related to other plant methyltransferases whose substrates range from isoflavones to phenylpropenes. The peak in the levels of OOMT1 and OOMT2 transcripts in the flowers coincides with peak OMT activity and with the emission of orcinol dimethyl ether.


Assuntos
Metiltransferases/metabolismo , Fenóis/metabolismo , Caules de Planta/enzimologia , Rosa/enzimologia , Sequência de Aminoácidos , Northern Blotting , Clonagem Molecular , DNA Complementar/química , DNA Complementar/genética , Cromatografia Gasosa-Espectrometria de Massas , Metiltransferases/genética , Dados de Sequência Molecular , Floroglucinol/metabolismo , Filogenia , Extratos Vegetais/metabolismo , RNA Mensageiro/metabolismo , Proteínas Recombinantes de Fusão/genética , Proteínas Recombinantes de Fusão/metabolismo , Resorcinóis/metabolismo , Rosa/genética , Análise de Sequência de DNA , Homologia de Sequência de Aminoácidos
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