Subunit composition of seed storage proteins in high-protein soybean genotypes

The objective of this work was to quantify the accumulation of the major seed storage protein subunits, β-conglycinin and glycinin, and how they influence yield and protein and oil contents in high-protein soybean genotypes. The relative accumulation of subunits was calculated by scanning SDS-PAGE gels using densitometry. The protein content of the tested genotypes was higher than control cultivar in the same maturity group. Several genotypes with improved protein content and with unchanged yield or oil content were developed as a result of new breeding initiatives. This research confirmed that high-protein cultivars accumulate higher amounts of glycinin and β-conglycinin. Genotypes KO5427, KO5428, and KO5429, which accumulated lower quantities of all subunits of glycinin and β-conglycinin, were the only exceptions. Attention should be given to genotypes KO5314 and KO5317, which accumulated significantly higher amounts of both subunits of glycinin, and to genotypes KO5425, KO5319, KO539 and KO536, which accumulated significantly higher amounts of β-conglycinin subunits. These findings suggest that some of the tested genotypes could be beneficial in different breeding programs aimed at the production of agronomically viable plants, yielding high-protein seed with specific composition of storage proteins for specific food applications.

Developmental changes in the heavy subunit of neurofilaments in the corpus callosum of the cat.

In the corpus callosum of the cat, the heavy subunit of neurofilaments (NFH) can be demonstrated with the monoclonal antibody NE14, as early as P11, not at P3, and only in a few axons. At P18-19 and more markedly at P29, many more callosal axons have become positive to NE14 and this is similar to what is found in the adult. In contrast, callosal axons become positive to the neurofilament antibody SMI-32 only between P29 and P39 and remain positive in the adult. Treatment with alkaline phosphatase prevents axonal staining with NE14, but results in SMI-32 staining of a few callosal axons as early as P11, but not at P3. Between P11 and P19 the number of axons stained with SMI-32 after alkaline phosphatase treatment increases, in parallel with that of axons stained with NE14. Thus NE14 appears to recognize a phosphorylated form of NFH, while SMI-32 appears to recognize an epitope of NFH which is either masked by phosphate or inaccessible until between P29 and P39, unless the tissue is treated with alkaline phosphatase. These two forms of NFH appear towards the end of the period of massive developmental elimination of callosal axons. They are also synchronous with changes in the spacing of neurofilaments quantified in a separate ultrastructural study. These cytoskeletal changes may terminate the juvenile-labile state of callosal axons and allow further axial growth of the axon.

1.° Alani Aurigae oratio ad Imperatorem dicta, nomine Legatorum Caroli VI. Regis Francorum. — 2.° Ejusdem epistola ad Gallos ad detestationem belli plusquam civilis, et suasionem pacis. — 3.° Dialogus familiaris amici et sodalis super deploratione Gallicae calamitatis : eodem authore. — 4.° Ejusdem persuasio ad Pragenses in fide deviantes, dicta praesente Caesare. — 5.° Ejusdem epistola ad Universitatem Parisiensem, post egressum dolorosum Regis Caroli VII. tunc Regentis, à civitate Parisiensi. — 6.° Ejusdem oratio ad Regem Romanorum Sigismundum. — 7.° Ejusdem epistola de vita curiali, ad Guillelmum Aurigam, fratrem suum, tunc Canonicum Parisiensem et Consiliarium regium, postea verò Episcopum Parisiensem. — 8.° Ejusdem in ingratum amicum invectiva. — 9.° Ejusdem in invidum et detractorem invectiva.

Colbertinus

1.° Alani Aurigae oratio ad Imperatorem dicta, nomine Legatorum Caroli VI. Regis Francorum. — 2.° Ejusdem epistola ad Gallos ad detestationem belli plusquam civilis, et suasionem pacis. — 3.° Dialogus familiaris amici et sodalis super deploratione Gallicae calamitatis : eodem authore. — 4.° Ejusdem persuasio ad Pragenses in fide deviantes, dicta praesente Caesare. — 5.° Ejusdem epistola ad Universitatem Parisiensem, post egressum dolorosum Regis Caroli VII. tunc Regentis, à civitate Parisiensi. — 6.° Ejusdem oratio ad Regem Romanorum Sigismundum. — 7.° Ejusdem epistola de vita curiali, ad Guillelmum Aurigam, fratrem suum, tunc Canonicum Parisiensem et Consiliarium regium, postea verò Episcopum Parisiensem. — 8.° Ejusdem in ingratum amicum invectiva. — 9.° Ejusdem in invidum et detractorem invectiva.

Colbertinus

El comercio con Africa y el Mediterraneo en las costas orientales de Hispania entre los siglos V y VII: las producciones cerámicas

Il risultato delle indagini condotte negli anni scorsi nei depositi archeologici della Catalogna, sia urbani, sia rurali, consente di determinare le tendenze delle importazioni e dell’economia in quest’area occidentale della penisola iberica fra il V secolo e la fine del VI-inizi del VII. In questa sede viene proposta una sintesi interpretativa dei dati disponibili, specialmente in rapporto al commercio delle ceramiche africane che costituivano le principali importazioni. Allo stato delle ricerche si possono avanzare alcune riflessioni. Se è vero che l’occupazione di Cartagine da parte dei Vandali nel 439 potrebbe aver determinato alcuni cambiamenti nella commercializzazione dei materiali africani, non va escluso che, tra la metà e la seconda metà del V secolo, il rafforzamento politico del regno vandalo abbia causato alcuni importanti cambiamenti tipologici nelle ceramiche africane (sigillata D, anfore) e un nuovo impulso alla relativa commercializzazione. Tra la seconda metà del VI secolo e la prima metà del VII (e forse anche la seconda metà) è proseguito l’arrivo di ceramica africana, proveniente soprattutto dall’area tunisina e, in minore quantità, dal Mediterraneo orientale. L’importazione di sigillata africana ha subito un significativo calo in questo periodo, ma non sparisce del tutto almeno fino agli inizi del VII secolo. Nel contempo è documentato un aumento considerevole della presenza di anfore africane, tanto che non può essere accolta l’ipotesi della cessazione delle importazioni tra la metà e il pieno VI secolo. Di conseguenza la rivalità politica fra i Visigoti e i Bizantini non si è tradotta nella scomparsa del commercio fra la penisola iberica e il Nord Africa, anche se è ben documentata una notevole diminuzione dei prodotti africani nel nord della provincia bizantina di Spania. La causa (o le cause) della fine dell’arrivo delle importazioni mediterranee lungo i litorali ispanici non può essere accertata con sicurezza. D’altra parte le ragioni di questo fenomeno vanno ricercate non solo nei centri di consumo, ma anche nelle aree di produzione, sicché sembra probabile che, come viene tradizionalmente ritenuto, la fine delle esportazioni fu determinata dall’invasione islamica dell’Africa settentrionale.

Effects of polymorphisms in beta1-adrenoceptor and alpha-subunit of G protein on heart rate and blood pressure during exercise test. The finnish cardiovascular study.

J Appl Physiol vol 100, no 2, pp 507-511, 2006

Dictionnaire historique et critique. T. VII, Gabriel-Hemmingius / de Pierre Bayle... ; éd. augm. de notes extraites de Chaufepié, Joly, La Monnoie, Leduchat, L.-J. Leclerc, Prosper Marchand, etc...

Collection : Archives de la linguistique française ; 30

Implication of DNA methylation, CTCF and BORIS factors in the transcriptional regulation of the human telomerase catalytic subunit hTERT

RESUME La télomérase confère une durée de vie illimitée et est réactivée dans la plupart des cellules tumorales. Sa sous-unité catalytique hTERT est définie comme le facteur limitant pour son activation. De l'identification de facteurs liant la région régulatrice d'hTERT, au rôle de la méthylation de l'ADN et de la modification des histones, de nombreux modèles de régulation ont été suggérés. Cependant, aucun de ces modèles n'a pu expliquer l'inactivation de la télomérase dans la plupart des cellules somatiques et sa réactivation dans la majorité des cellules tumorales. De plus, les observations contradictoires entre le faible niveau d'expression d'ARN messager d'hTERT dans les cellules télomérase-positives et la très forte activité transcriptionnelle du promoteur d'hTERT en transfection restent incomprises. Dans cette étude, nous avons montré que la région proximale du gène hTERT (exon 1 et 2) était impliquée dans la répression de l'activité de son promoteur. Nous avons identifié le facteur CTCF comme étant un inhibiteur du promoteur d'hTERT, en se liant au niveau de son premier exon. La méthylation de l'exon 1 du gène hTERT, couramment observée dans les tumeurs mais pas dans les cellules normales, empêcherait la liaison de CTCF. L'étude du profil de méthylation du promoteur d'hTERT indique qu'une partie du promoteur reste déméthylée et qu'elle semble suffisante pour permettre une faible activité transcriptionnelle du gène hTERT. Ainsi, la méthylation particulière des régions régulatrices d'hTERT inhibe la liaison de CTCF tout en permettant une faible transcription du gène. Cependant, dans certaines cellules tumorales, le promoteur et la région proximale du gène hTERT ne sont pas méthylés. Dans les lignées cellulaires tumorales de tesitcules et d'ovaires, l'inhibition de CTCF est contrée par son paralogue BORIS, qui se lie aussi au niveau de l'exon 1 d'hTERT, mais permet ainsi l'activation du promoteur. L'étude de l'expression du gène BORIS montre qu'il est exclusivement exprimé dans les tissus normaux de testicules et d'ovaires jeunes, ainsi qu'à différents niveaux dans la plupart des tumeurs. Sa transcription est sous le contrôle de deux promoteurs. Le promoteur proximal est régulé par méthylation et un transcrit alternatif majoritaire, délété de l'exon 6, est trouvé lorsque ce promoteur est actif. Tous ces résultats conduisent à un modèle de régulation du gène hTERT qui tient compte du profil épigénétique du gène et qui permet d'expliquer le faible taux de transcription observé in vivo. De plus, l'expression de BORIS dans les cancers et son implication dans l'activation du gène hTERT pourrait permettre de comprendre les phénomènes de dérégulation épigénétique et d'immortalisation qui ont lieu durant la tumorigenèse. SUMMARY Telomerase confers an unlimited lifespan, and is reactivated in most tumor cells. The catalytic subunit of telomerase, hTERT, is defined as the limiting factor for telomerase activity. Between activators and repressors that bind to the hTERT 5' regulatory region, and the role of CpG methylation and histone acetylation, an abundance of regulatory models have been suggested. None of these models can explain the silence of telomerase in most somatic cells and its reactivation in tumor cells. Moreover, the contradictory observations of the low level of hTERT mRNA in telomerase-positive cells and the high transcriptional activity of the hTERT promoter in transfection experiments remain unresolved. In this study, we demonstrated that the proximal exonic region of the hTERT gene (exon 1 and 2) is involved in the inhibition of its promoter. We identified the protein CTCF as the inhibitor of the hTERT promoter, through its binding to the first exon. The methylation of the first exon region, which is often observed in cancer cells but not in noimal cells, represses CTCF binding. Study of hTERT promoter methylation shows a partial demethylation sufficient to activate the transcription of the hTERT gene. Therefore, we demonstrated that the particular methylation profile of the hTERT regulatory sequences inhibits the binding of CTCF, while it allows a low transcription of the gene. Nevertheless, in some tumor cells, the promoter and the proximal exonic region of hTERT are unmethylated. In testicular and ovarian cancer cell lines, CTCF inhibition is counteracted by its BORIS paralogue that also binds the hTERT first exon but allows the promoter activation. The study of BORIS gene regulation showed that this factor is exclusively expressed in normal tissue of testis and ovary of young woman, as well as in almost all tumors with different levels. Two promoters were found to induce its transcription. The proximal promoter was regulated by methylation. Moreover, a major alternative transcript, deleted of the exon 6, is detected when this promoter is active. All these results lead to a model for hTERT regulation that takes into account the epigenetic profile of the gene and provides an explanation for the low transcriptional level observed in vivo. BORIS expression in cancers and its implication in hTERT activation might also permit the understanding of epigenetic deregulation and immortalization phenomena that occur during tumorigenesis.

Ferran VII "el cruel": la repressió dels Liberals a la Lleida de la Dècada Ominosa

En este estudio se pretende analizar la represión efectuada por el gobierno absolutista de Fernando VII durante su segunda reinstauración, la historiográficamente llamada Década Ominosa, hacia los liberales a Lleida. Mientras que los realistas solicitaron premios y prerrogativas por los servicios prestados en defensa de la Religión y la Monarquía las autoridades absolutistas implantaron de nuevo la censura, prohibieron cualquier vestigio legislativo liberal, depuraron los antiguos funcionarios constitucionales, a los milicianos nacionales, a los miembros de la Junta Patriótica y a los políticos liberales en general. Por tanto, el indulto y el perdón general del año 1824 fue insuficiente, sobretodo en la medida que permitió represaliar de manera arbitraria a cualquier individuo relacionado con cualquier espacio de poder durante el Trienio Liberal. Finalmente cabe destacar la exoneración de los derechos civiles y los oficios que sufrieron figuras liberales tan relevantes como los escribanos Marià Hostalrich o Francesc Xavier Soldevila.