Effects of plant growth promoting rhizobacteria (PGPR) on Citrus macrophylla rootstock

Citrus is one of the largest fruit crops grown in Morocco. Citrus crops gain in importance due to the jobs generated during the production process of fresh or processed fruit. Intensive agriculture is characterized by the excessive use of inorganic fertilizers and pesticides. This production system has generated serious environmental contamination problems, thus, it is necessary to implement sustainable production strategies to reduce the use of synthetic chemicals and contribute to soil and water conservation. In this context, Seventy two Rhizobacterial isolates of fluorescent Pseudomonas were isolated from rhizosphere soil of Citrus in the Sapiama nursery. These isolates were tested on germination and growth of Citrus macrophylla rootstock. The results obtained showed that the isolate C11 significantly stimulated germination 16 days after seed inoculation. The C26, C6 and C24 isolates showed PGPR effects improving significantly the growth parameters of C. macrophylla rootstock. They significantly promoted plant height, collar diameter and root length. This study concluded that the Pseudomonas isolates could be potential alternative biofertilizers to chemical products and could be considered as a promising main component for sustainable agriculture development strategy in Citrus farming. Keywords: Citrus macrophylla, Pseudomonas, PGP

The localization of amyloid precursor protein to ependymal cilia in vertebrates and its role in ciliogenesis and brain development in zebrafish

Amyloid precursor protein (APP) is expressed in many tissues in human, mice and in zebrafish. In zebrafish, there are two orthologues, Appa and Appb. Interestingly, some cellular processes associated with APP overlap with cilia-mediated functions. Whereas the localization of APP to primary cilia of in vitro-cultured cells has been reported, we addressed the presence of APP in motile and in non-motile sensory cilia and its potential implication for ciliogenesis using zebrafish, mouse, and human samples. We report that Appa and Appb are expressed by ciliated cells and become localized at the membrane of cilia in the olfactory epithelium, otic vesicle and in the brain ventricles of zebrafish embryos. App in ependymal cilia persisted in adult zebrafish and was also detected in mouse and human brain. Finally, we found morphologically abnormal ependymal cilia and smaller brain ventricles in appa-/-appb-/- mutant zebrafish. Our findings demonstrate an evolutionary conserved localisation of APP to cilia and suggest a role of App in ciliogenesis and cilia-related functions

Rhizospheric solutions: Pseudomonas isolates counter Botrytis cinerea on tomato

La moisissure grise causée par Botrytis cinerea provoque des dégâts sur plus de 200 espèces de cultures dans le monde. B. cinerea sporule pour former une pourriture grise sur les feuilles, les tiges et les fruits. Pour lutter contre B. cinerea, des fongicides synthétiques sont utilisés. Ces derniers mettent en danger la santé humaine et environnementale en plus de la résistance qu'ils peuvent occasionner chez les souches de B. cinerea. Les alternatives écologiques sont des solutions appropriées pour contrôler la moisissure grise tout en maintenant l’équilibre environnemental. L’objectif de cette étude est d'évaluer l’effet des isolats de Pseudomonas issus de la rhizosphère de la tomate sur B. cinerea. Les résultats ont montré que les 76 isolats testés inhibent le développement de B. cinerea in vitro. Cinq isolats de Pseudomonas (Q6B, Q13B, Q7B, Q14B et Q1B) ont provoqué des niveaux d'inhibition significatifs allant de 65 à 73%. Par ailleurs, ces isolats ont également inhibé B. cinerea sur les feuilles et le fruit de la tomate. Pour tenter d'élucider les mécanismes d'action, les cinq isolats ont montré une production des métabolites antifongiques tels que les sidérophores, le cyanure d'hydrogène et d’autres enzymes. Les résultats de cette étude ont montré que les isolats de Pseudomonas Q6B, Q13B, Q7B, Q14B et Q1B ont une forte efficacité dans la lutte biologique contre B. cinerea et peuvent être utilisés pour une lutte écologique durable.Gray mold caused by Botrytis cinerea causes serious losses in more than 200 crop species worldwide. The necrotrophic fungus sporulates to effect a grey covering on leaves, stems and flowers. B. cinerea is controlled by chemical synthetic fungicides, endangering human and environmental health. Synthetic fungicides stimulate emergence of pathogen resistance. Organic alternatives which may be present or introduced into the edaphic environment are suitable solutions to control outbreaks. This study was done in order to elucidate the mode of action involved in the control of B. cinerea using fluorescent Pseudomonas isolates from tomato roots. The results show that all 76 isolates inhibit fungal growth during in vitro bioassay using dual culture technique. Five isolates of Pseudomonas (Q6B, Q13B, Q7B, Q14B and Q1B) cause significant inhibition levels ranging from 65 to 73%. These isolates inhibit fungal growth in both fruits and leaves. Each isolate tested produced antifungal metabolites (siderophores, hydrogen cyanide and enzymes). Results of this study show that all tested Pseudomonas isolates have a strong efficacy in biological control against B. cinerea and can be used for environmentally sustainable control

Preferential binding of a stable G3BP ribonucleoprotein complex to intron-retaining transcripts in mouse brain and modulation of their expression in the cerebellum.

Neuronal granules play an important role in the localization and transport of translationally silenced messenger ribonucleoproteins (mRNPs) in neurons. Among the factors associated with these granules, the RNA-binding protein G3BP1 (stress-granules assembly factor) is involved in neuronal plasticity and is induced in Alzheimer's disease. We immunopurified a stable complex containing G3BP1 from mouse brain and performed High-Throughput Sequencing and CrossLinking Immunoprecipitation (HITS-CLIP) to identify the associated RNAs. The G3BP-complex contained the deubiquitinating protease USP10, CtBP1 and the RNA binding proteins Caprin-1, G3BP2a and SFPQ (Splicing Factor Proline and Glutamine rich, or PSF). The G3BP-complex binds preferentially to transcripts that retain introns, and to non-coding sequences like 3'UTR and long non-coding RNAs. Specific transcripts with retained introns appear to be enriched in the cerebellum compared to the rest of the brain and G3BP1 depletion decreased this intron retention in the cerebellum of G3BP1 knockout mice. Among the enriched transcripts, we found an overrepresentation of genes involved in synaptic transmission, especially glutamate-related neuronal transmission. Notably, G3BP1 seems to repress the expression of the mature Grm5 (metabotropic glutamate receptor 5) transcript, by promoting the retention of an intron in the immature transcript in the cerebellum. Our results suggest that G3BP is involved in a new functional mechanism to regulate non-coding RNAs including intron-retaining transcripts, and thus have broad implications for neuronal gene regulation, where intron retention is widespread. This article is protected by copyright. All rights reserved

Evaluacija svojstava vezanja sluzi sjemenki biljke Plantago psyllium

Mucilage extracted from Plantago psyllium seeds was evaluated for inertness and safety parameters. The suitability of psyllium mucilage for a pharmaceutical binder was assessed in paracetamol tablets. Properties of the granules prepared using different concentrations of psyllium mucilage was compared with PVP and tragacanth. Psyllium mucilage at 5 % (m⁄m) level was found to be comparable with 3 % (m⁄m) of PVP. Investigated paracetamol tablets indicated that psyllium mucilage can retard the drug release.U radu je ispitivana neškodljivost i sigurnost uporabe sluzi ekstrahirane iz sjemenki biljke Plantago psyllium. Primjenjivost te sluzi kao veziva u farmaceutskim pripravcima ispitana je na tabletama paracetamola. Granule pripravljene s različitim koncentracijama sluzi uspoređene su s granulama s PVP-om i tragakantom. Sluz s udjelom 5 % (m/m) usporediva je s otopinom PVP-a masenog udjela 3 %. Pripravljene tablete paracetamola ukazuju na to da ispitivana sluz može usporiti oslobađanje lijeka

A Novel Mouse c-fos Intronic Promoter That Responds to CREB and AP-1 Is Developmentally Regulated In Vivo

BACKGROUND: The c-fos proto-oncogene is an archetype for rapid and integrative transcriptional activation. Innumerable studies have focused on the canonical promoter, located upstream from the transcriptional start site. However, several regulatory sequences have been found in the first intron. METHODOLOGY/PRINCIPAL FINDINGS: Here we describe an extremely conserved region in c-fos first intron that contains a putative TATA box, and functional TRE and CRE sites. This fragment drives reporter gene activation in fibroblasts, which is enhanced by increasing intracellular calcium and cAMP and by cotransfection of CREB or c-Fos/c-Jun expression vectors. We produced transgenic mice expressing a lacZ reporter controlled by the intronic promoter. Lac Z expression of this promoter is restricted to the developing central nervous system (CNS) and the mesenchyme of developing mammary buds in embryos 12.5 days post-conception, and to brain tissue in adults. RT-QPCR analysis of tissue mRNA, including the anlage of the mammary gland and the CNS, confirms the existence of a novel, nested mRNA initiated in the first intron. CONCLUSIONS/SIGNIFICANCE: Our results provide evidence for a novel, developmentally regulated promoter in the first intron of the c-fos gene

Characterization of callase (β-1,3-d-glucanase) activity during microsporogenesis in the sterile anthers of Allium sativum L. and the fertile anthers of A. atropurpureum

We examined callase activity in anthers of sterile Allium sativum (garlic) and fertile Allium atropurpureum. In A. sativum, a species that produces sterile pollen and propagates only vegetatively, callase was extracted from the thick walls of A. sativum microspore tetrads exhibited maximum activity at pH 4.8, and the corresponding in vivo values ranged from 4.5 to 5.0. Once microspores were released, in vitro callase activity peaked at three distinct pH values, reflecting the presence of three callase isoforms. One isoform, which was previously identified in the tetrad stage, displayed maximum activity at pH 4.8, and the remaining two isoforms, which were novel, were most active at pH 6.0 and 7.3. The corresponding in vivo values ranged from pH 4.75 to 6.0. In contrast, in A. atropurpureum, a sexually propagating species, three callase isoforms, active at pH 4.8–5.2, 6.1, and 7.3, were identified in samples of microsporangia that had released their microspores. The corresponding in vivo value for this plant was 5.9. The callose wall persists around A. sativum meiotic cells, whereas only one callase isoform, with an optimum activity of pH 4.8, is active in the acidic environment of the microsporangium. However, this isoform is degraded when the pH rises to 6.0 and two other callase isoforms, maximally active at pH 6.0 and 7.3, appear. Thus, factors that alter the pH of the microsporangium may indirectly affect the male gametophyte development by modulating the activity of callase and thereby regulating the degradation of the callose wall