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1.
Environ Pollut ; 215: 331-339, 2016 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-27236494

RESUMEN

In this study, the interactions between microplastics, chosen among the most widely used in industry such as polypropylene (PP) and high-density polyethylene (HDPE), and a model freshwater microalgae, Chlamydomas reinhardtii, were investigated. It was shown that the presence of high concentrations of microplastics with size >400 µm did not directly impact the growth of microalgae in the first days of contact and that the expression of three genes involved in the stress response was not modified after 78 days. In parallel, a similar colonization was observed for the two polymers. However, after 20 days of contact, in the case of PP only, hetero-aggregates constituted of microalgae, microplastics and exopolysaccharides were formed. An estimation of the hetero-aggregates composition was approximately 50% of PP fragments and 50% of microalgae, which led to a final density close to 1.2. Such hetero-aggregates appear as an important pathway for the vertical transport of PP microplastics from the water surface to sediment. Moreover, after more than 70 days of contact with microplastics, the microalgae genes involved in the sugar biosynthesis pathways were strongly over-expressed compared to control conditions. The levels of over-expression were higher in the case of HDPE than in PP condition. This work presents the first evidence that depending on their chemical nature, microplastics will follow different fates in the environment.


Asunto(s)
Agua Dulce/química , Microalgas/crecimiento & desarrollo , Tamaño de la Partícula , Polietileno/química , Polímeros/química , Polipropilenos/química , Contaminantes Químicos del Agua/análisis , Monitoreo del Ambiente , Expresión Génica , Sedimentos Geológicos , Microalgas/genética , Plásticos/química , Polisacáridos/química , Agua/química , Contaminación del Agua
2.
PLoS One ; 8(4): e62450, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23658632

RESUMEN

Gynodioecy, the coexistence of hermaphrodites and females (i.e. male-sterile plants) in natural plant populations, most often results from polymorphism at genetic loci involved in a particular interaction between the nuclear and cytoplasmic genetic compartments (cytonuclear epistasis): cytoplasmic male sterility (CMS). Although CMS clearly contributes to the coevolution of involved nuclear loci and cytoplasmic genomes in gynodioecious species, the occurrence of CMS genetic factors in the absence of sexual polymorphism (cryptic CMS) is not easily detected and rarely taken in consideration. We found cryptic CMS in the model plant Arabidopsis thaliana after crossing distantly related accessions, Sha and Mr-0. Male sterility resulted from an interaction between the Sha cytoplasm and two Mr-0 genomic regions located on chromosome 1 and chromosome 3. Additional accessions with either nuclear sterility maintainers or sterilizing cytoplasms were identified from crosses with either Sha or Mr-0. By comparing two very closely related cytoplasms with different male-sterility inducing abilities, we identified a novel mitochondrial ORF, named orf117Sha, that is most likely the sterilizing factor of the Sha cytoplasm. The presence of orf117Sha was investigated in worldwide natural accessions. It was found mainly associated with a single chlorotype in accessions belonging to a clade predominantly originating from Central Asia. More than one-third of accessions from this clade carried orf117Sha, indicating that the sterilizing-inducing cytoplasm had spread in this lineage. We also report the coexistence of the sterilizing cytoplasm with a non-sterilizing cytoplasm at a small, local scale in a natural population; in addition a correlation between cytotype and nuclear haplotype was detected in this population. Our results suggest that this CMS system induced sexual polymorphism in A. thaliana populations, at the time when the species was mainly outcrossing.


Asunto(s)
Arabidopsis/genética , Sitios Genéticos , Mitocondrias/genética , Proteínas Mitocondriales/genética , Infertilidad Vegetal/genética , Arabidopsis/clasificación , Evolución Biológica , Núcleo Celular/genética , Cromosomas de las Plantas , Cruzamientos Genéticos , Citoplasma/genética , Sistemas de Lectura Abierta , Filogenia
3.
Gene ; 509(1): 7-15, 2012 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-22921893

RESUMEN

Transposable elements (TEs) are present in roughly all genomes. These mobile DNA sequences are able to invade genomes and their impact on genome evolution is substantial. The mobility of TEs can induce the appearance of deleterious mutations, gene disruption and chromosome rearrangements, but transposition activity also has positive aspects and the mutational activities of TEs contribute to the genetic diversity of organisms. This short review aims to give a brief overview of the impact TEs may have on animal and plant genome structure and expression, and the relationship between TEs and the stress response of organisms, including insecticide resistance.


Asunto(s)
Elementos Transponibles de ADN , Tamaño del Genoma , Adaptación Biológica/genética , Animales , Eucariontes/genética , Evolución Molecular , Regulación de la Expresión Génica , Reordenamiento Génico , Estrés Fisiológico/genética
4.
Plant Mol Biol ; 70(1-2): 123-37, 2009 May.
Artículo en Inglés | MEDLINE | ID: mdl-19199092

RESUMEN

The Ogura cytoplasmic male sterility causing protein, ORF138, was found to be part of a complex with an apparent size of over 750 kDa in the inner membrane of mitochondria of sterile plants. ORF138 did not colocalize with any of the oxidative phosphorylation complexes, nor did its presence modify their apparent size or amount, compared to samples from fertile isogenic plants. We attempted to detect potential proteins or nucleic acids that could be involved in the large ORF138 complex by 2D PAGE, immunoprecipitation and nuclease treatments of native extracts. All our results suggest that the ORF138 protein is the main, if not only, component of this large complex. The capacities of complexes I, II, IV, and ATP synthase were identical in samples from sterile and fertile plants. Isolated mitochondria from sterile plants showed a higher oxygen consumption than those from fertile plants. In vivo respiration measurements suggest that the difference in O(2) consumption measured at the organelle level is compensated at the cell/tissue level, completely in leaves, but only partially in male reproductive organs.


Asunto(s)
Brassica rapa/metabolismo , Mitocondrias/metabolismo , Proteínas Mitocondriales/metabolismo , Infertilidad Vegetal , Proteínas de Plantas/metabolismo , Brassica rapa/genética , Electroforesis en Gel de Poliacrilamida , Proteínas Mitocondriales/genética , Fosforilación Oxidativa , Consumo de Oxígeno , Proteínas de Plantas/genética
5.
Theor Appl Genet ; 114(8): 1333-43, 2007 May.
Artículo en Inglés | MEDLINE | ID: mdl-17318491

RESUMEN

The Ogura cytoplasmic male sterility (CMS) of radish has been used for hybrid seed production in radish and Brassica crops. It is the only CMS system occurring in wild populations for which the gene responsible for sterility and a restorer gene have been formally identified. In Japan, gynodioecious populations of radish carrying Ogura or an Ogura-related cytoplasm have been described. The occurrence of restorer genes for the Ogura CMS in wild radish (Raphanus raphanistrum) in France led us to search for the corresponding male sterility gene (orf138) in several natural populations in France, England and Lebanon. We detected the orf138 gene, by PCR, at low frequency, in three populations from France and one from Southern England. Further molecular characterization showed that these plants carried a cytoplasm closely related to the original Ogura cytoplasm, with a variant orf138 coding sequence, previously reported to be ancestral. We performed crosses with sterile and maintainer radish lines, to test the ability of this wild Ogura-related cytoplasm to induce sterility. Surprisingly, the European Ogura-related cytoplasm did not cause sterility. Northern blots and circular RT-PCR analyses showed that orf138 gene expression was impaired in these plants because of a novel cytoplasm-dependent transcript-processing site.


Asunto(s)
Citoplasma/genética , Proteínas Mitocondriales/genética , Infertilidad Vegetal/genética , Proteínas de Plantas/genética , Raphanus/genética , Supresión Genética , Islas Anglonormandas , Citoplasma/fisiología , Inglaterra , Francia , Líbano , Proteínas Mitocondriales/fisiología , Infertilidad Vegetal/fisiología , Proteínas de Plantas/fisiología , Raphanus/fisiología , Caracteres Sexuales
6.
Biochimie ; 87(12): 1089-100, 2005 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-15979231

RESUMEN

In cytoplasmic male sterility (CMS), original mitochondrial genes contribute to sex determinism by provoking pollen abortion. The function of the encoded proteins remains unclear. We studied the ORF138 protein, responsible for the 'Ogura' CMS, which is both used in hybrid seed production and present in natural populations. We analyzed the biochemical and structural properties of this protein in male-sterile plants and in E. coli. We showed that this protein spontaneously forms dimers in vitro. Truncated variants of the protein, containing either the hydrophobic or the hydrophilic moiety, also spontaneously dimerize. By fractionating mitochondria, we showed that ORF138 was strongly associated with the inner mitochondrial membrane of male-sterile plants. Our results also strongly suggest that ORF138 forms oligomers in male-sterile plant mitochondria. In E. coli, ORF138 was associated with the plasma membrane, as shown by membrane fractionation, and formed oligomers. The production of this protein strongly inhibited bacterial growth, but not by inhibiting respiration. The observed toxic effects required both the hydrophilic and hydrophobic moieties of the protein.


Asunto(s)
Brassica/metabolismo , Mitocondrias/metabolismo , Proteínas Mitocondriales/química , Proteínas Mitocondriales/metabolismo , Infertilidad Vegetal , Proteínas de Plantas/química , Proteínas de Plantas/metabolismo , Secuencia de Bases , Cartilla de ADN , Escherichia coli/genética , Escherichia coli/crecimiento & desarrollo , Cinética , Proteínas Mitocondriales/genética , Proteínas de Plantas/genética , Plásmidos , Reproducción , Mapeo Restrictivo
7.
EMBO J ; 21(11): 2591-601, 2002 Jun 03.
Artículo en Inglés | MEDLINE | ID: mdl-12032072

RESUMEN

Heat shock factor 2, one of the four vertebrate HSFs, transcriptional regulators of heat shock gene expression, is active during embryogenesis and spermatogenesis, with unknown functions and targets. By disrupting the Hsf2 gene, we show that, although the lack of HSF2 is not embryonic lethal, Hsf2(-/-) mice suffer from brain abnormalities, and meiotic and gameto genesis defects in both genders. The disturbances in brain are characterized by the enlargement of lateral and third ventricles and the reduction of hippocampus and striatum, in correlation with HSF2 expression in proliferative cells of the neuroepithelium and in some ependymal cells in adults. Many developing spermatocytes are eliminated via apoptosis in a stage-specific manner in Hsf2(-/-) males, and pachytene spermatocytes also display structural defects in the synaptonemal complexes between homologous chromosomes. Hsf2(-/-) females suffer from multiple fertility defects: the production of abnormal eggs, the reduction in ovarian follicle number and the presence of hemorrhagic cystic follicles are consistent with meiotic defects. Hsf2(-/-) females also display hormone response defects, that can be rescued by superovulation treatment, and exhibit abnormal rates of luteinizing hormone receptor mRNAs.


Asunto(s)
Encéfalo/anomalías , Encéfalo/metabolismo , Cromosomas/ultraestructura , Proteínas de Choque Térmico/genética , Infertilidad Femenina/genética , Meiosis , Factores de Transcripción/genética , Alelos , Animales , Apoptosis , Western Blotting , Embrión de Mamíferos/metabolismo , Femenino , Fertilidad/genética , Vectores Genéticos , Genotipo , Heterocigoto , Inmunohistoquímica , Operón Lac , Masculino , Ratones , Ratones Transgénicos , Microscopía Fluorescente , Modelos Genéticos , Ovario/metabolismo , Regiones Promotoras Genéticas , Recombinación Genética , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Factores Sexuales , Testículo/metabolismo , Factores de Tiempo , beta-Galactosidasa/metabolismo
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