Fruit Load and Root Development in Field-Grown Loquat Trees (Eriobotrya japonica Lindl)

Photosynthate translocation to the root in loquat trees decreases as fruit develops. Thus, during the most active period of fruit development, that is, from 50 % of its final size to the beginning of fruit color change, which correspond to BBCH growth scale stages 705 and 801, both translocating and reducing carbohydrate concentrations diminish greatly. Concomitantly, the results from our experiment show an increased abscisic acid (ABA) concentration and a decrease in the respiration rate detected by an accumulation of glucose-6-phosphate, which paralleled a reduced indole-3-acetic acid (IAA) concentration in roots. As a consequence, root development was strongly and significantly reduced. Because loquat fruit develops in winter and nonshoot growth takes place at this time, our results show that root development in loquat trees is controlled by the fruit, mediated by competition for carbohydrates and modulated by hormones. The experiment was conducted using field-grown loquat during two consecutive years and by comparing fruiting and defruited trees. Fruits were detached from the trees in the early fruit developmental stage (10 % of final size, 701 BBCH growth scale), and carbohydrate concentrations in leaves, shoot bark, and roots, as well as nitrogen fractions (N–NO₃ ^?, N–NH₄ ⁺, and N–proteinaceous) and hormone (IAA, zeatin, and ABA) concentrations in roots, were analyzed throughout the period of fruit development. Root development was evaluated by counting the emerging lateral root primordia during the fruit developmental stages BBCH growth scale 701–809 (fruit color fully developed).     

Functional and structural characterization of the first prokaryotic member of the L-amino acid transporter (LAT) family: a model for APC transporters

We have identified YkbA from Bacillus subtilis as a novel member of the L-amino acid transporter (LAT) family of amino acid transporters. The protein is approximately 30% identical in amino acid sequence to the light subunits of human heteromeric amino acid transporters. Purified His-tagged YkbA from Escherichia coli membranes reconstituted in proteoliposomes exhibited sodium-independent, obligatory exchange activity for L-serine and L-threonine and also for aromatic amino acids, albeit with less activity. Thus, we propose that YkbA be renamed SteT (Ser/Thr exchanger transporter). Kinetic analysis supports a sequential mechanism of exchange for SteT. Freeze-fracture analysis of purified, functionally active SteT in proteoliposomes, together with blue native polyacrylamide gel electrophoresis and transmission electron microscopy of detergent-solubilized purified SteT, suggest that the transporter exists in a monomeric form. Freeze-fracture analysis showed spherical particles with a diameter of 7.4 nm. Transmission electron microscopy revealed elliptical particles (diameters 6 x 7 nm) with a distinct central depression. To our knowledge, this is the first functional characterization of a prokaryotic member of the LAT family and the first structural data on an APC (amino acids, polyamines, and choline for organocations) transporter. SteT represents an excellent model to study the molecular architecture of the light subunits of heteromeric amino acid transporters and other APC transporters.     

Heparin activates Wnt signaling for neuronal morphogenesis

Wnt factors are secreted ligands that affect different aspects of the nervous system behavior like neurodevelopment, synaptogenesis and neurodegeneration. In different model systems, Wnt signaling has been demonstrated to be regulated by heparan sulfate proteoglycans (HSPGs). Whether HSPGs modulate Wnt signaling in the context of neuronal behavior is currently unknown. Here we demonstrate that activation of Wnt signaling with the endogenous ligand Wnt-7a results in an increased of neurite outgrowth in the neuroblastoma N2a cell line. Interestingly, heparin induces glycogen synthase kinase-3beta (GSK-3beta) inhibition, beta-catenin stabilization and morphological differentiation in both N2a cells and in rat primary hippocampal neuronal cultures. We also show that heparin modulates Wnt-3a-induced stabilization of beta-catenin. Several extracellular matrix and membrane-attached HSPGs were found to be expressed in both in vitro neuronal models. Changes in the expression of specific HSPGs were observed upon differentiation of N2a cells. Taken together, our findings suggest that HSPGs may modulate canonical Wnt signaling for neuronal morphogenesis.     

The evolutionary history of Drosophila buzzatii. XVI. Fitness component analysis in an original natural population from Argentina

The adaptive significance of the chromosomal polymorphism of Drosophila buzzati has been studied by means of fitness component analysis in an original population from Argentina. The results show evidence of selection acting through pupal viability, longevity (adult viability) and fecundity on the second chromosome polymorphism, and through pupal viability and virility on the fourth chromosome polymorphism. Changes in chromosomal inversion frequencies throughout the life-cycle suggested an endocyclic pattern of directional selection, which at first seems to be the only detectable mechanism responsible for the maintenance of the polymorphism. However, slow, long-term frequency changes cannot be ruled out. The way in which endocyclic selection acts on this population is different from that in a colonized population previously studied; that is, different fitness components are involved in the maintenance of chromosomal polymorphism. The possible factors that may explain these differences are discussed.     

Separate Binding and Functional Sites for ω co-Conotoxin and Nitrendipine Suggest Two Types of Calcium Channels in Bovine Chromaffin Cells

Purified adrenomedullary plasma membranes contain two high-affinity binding sites for 125I-omega-conotoxin, with KD values of 7.4 and 364 pM and Bmax values of 237 and 1,222 fmol/mg of protein, respectively. Dissociation kinetics showed a biphasic component and a high stability of the toxin-receptor complex, with a t1/2 of 81.6 h for the slow dissociation component. Unlabeled omega-conotoxin inhibited the binding of the radioiodinated toxin, adjusting to a two-site model with Ki1 of 6.8 and Ki2 of 653 pM. Specific binding was not affected by Ca2+ channel blockers or activators, cholinoceptor antagonists, adrenoceptor blockers, Na+ channel activators, dopaminoceptor blockers, or Na+/H+ antiport blockers, but divalent cations (Ca2+, Sr2+, and Ba2+) inhibited the toxin binding in a concentration-dependent manner. The binding of the dihydropyridine [3H]nitrendipine defined a single specific binding site with a KD of 490 pM and a Bmax of 129 fmol/mg of protein. At 0.25 microM, omega-conotoxin was not able to block depolarization-evoked Ca2+ uptake into cultured bovine adrenal chromaffin cells depolarized with 59 mM K+ for 30 s, whereas under the same conditions, 1 microM nitrendipine inhibited uptake by approximately 60%. When cells were hyperpolarized with 1.2 mM K+ for 5 min and then Ca2+ uptake was subsequently measured during additions of 59 mM K+. Omega-conotoxin partially inhibited Ca2+ uptake in a concentration-dependent manner. These results suggest that two different types of Ca2+ channels might be present in chromaffin cells. However, the molecular identity of omega-conotoxin binding sites remains to be determined.     

Soluble adenylate cyclase activity in Neurospora crassa.

A soluble form of adenylate cyclase was extracted from mycelia of Neurospora crassa wild-type strains. This enzyme activity was purified by chromatography on hexyl-amino-Sepharose, agarose and Blue Sepharose and preparative polyacrylamide-gel electrophoresis. On sodium dodecyl sulphate/polyacrylamide-gel electrophoresis, peak fractions from the later purification steps showed a main polypeptide band with an apparent molecular weight of about 66 000. The following hydrodynamic and molecular parameters were established for the Neurospora soluble adenylate cyclase activity: sedimentation coefficient, 6.25 S; Stokes radius, 7.3 nm; partial specific volume, 0.74 ml/g; molecular weight, 202 000; frictional ratio, 1.65. The isoelectric point of this enzyme activity was 4.65. The enzyme was not activated by GTP, [beta gamma-imido]GTP, fluoride or cholera toxin.     

Muscarinic receptor subtypes in bovine adrenal medulla

Catecholamine secretion in the bovine adrenal medulla is evoked largely by nicotinic receptor activation. However, bovine adrenal medulla also contain muscarinic receptors that mediate several cell responses. To understand the physiological role of muscarinic receptors in the bovine adrenal medulla it is important to identify the pharmacological subtypes present in this tissue. For this, we analyzed the abilities of differnt selective muscarinic antagonists in displacing the binding of the non-selective antagonist [3H] quinuclidinyl benzylate to an enriched plasma membrane fraction prepared from bovine adrenal medulla. All the selective antagonists bind at least two bindings sites with different affinities. The binding profile of the sites with high proportion is similar to the M2 subtype and those present in low proportion have a M1 profile. However, some variation in the proportion of the sites for the different ligands suggest the presence of the third pharmacological subtype (M3). We conclude that the sites in high proportion (60–80%) correspond to M2 muscarinic subtypes, and the rest is constitute by M1 plus M3 subtypes. The presence of multiplicity of subtypes in the adrenal medulla membranes suggests a diversity of functions of muscarinic receptors in the adrenal gland.Abbreviations [3H]QNB [3H]quinuclidinyl benzylate - HHSiD hexahydro-siladifenidol-hydrochloride - AF-DX 116 11-[[2-(diethylamino)methyl]]-1-piperidinyl]-5,11-dihydro-6H-pyrido[2,3,-b][1,4]benzodiazepin-6-one - 4-DAMP 4-diphenylacetoxy-N-methyl piperidine methobromide     

Multiple autosomal polymorphism in populations of Akodon simulator simulator Thomas, 1916 from Tucumán,Argentina (Rodentia,Cricetidae)

Cytogenetic analysis was performed on twenty seven specimens of Akodon simulator simulator collected in three different localities of Tucumán Province, Argentina. Diploid number, chromosomal morphology and C and G banding patterns were studied. Eight different karyomorphs were found, with diploid numbers of 2n=38, 39, 40, 41, and 42. All individuals showed the same number of chromosomal arms (FN=42). G-bands enable to identify chromosomal pairs (1, 10, 11, 12, 13, and 14) involved in three centric fusions. C-bands revealed that the heterochromatin is located in centromeric regions of the telocentric and biarmed chromosomes. The present study allowed us to document a new example of a floating multiple Robertsonian fusion polymorphism. The data are discussed in relation to the occurrence of Robertsonian polymorphism in natural populations.

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Resumen Polimorfismo autosómico múltiple en poblaciones de Akodon simulator simulator Thomas, 1916 de Tucumán, Argentina (Rodentia, Cricetidae). Se realizó un análisis citogenético de 27 especímenes de Akodon simulator simulator colectados en tres localidades diferentes de la provincia de Tucumán, Argentina. Se determinó el número diploide, la morfología cromosómica y los patrones de bandeo C y G. Se encotraron 8 cariomorfos differentes, con números diploides de 2n=38, 39, 40, 41, y 42. Todos los individuos presentaron el mismo número de brazos cromosómicos (FN=42). Las bandas G permitieron identificar los pares cromosómicos (1, 10, 11, 12, 13, y 14) involucrados en tres fusiones céntricas y las bandas C revelaron que la heterocromatina está localizada en las regiones centroméricas de los cromosomas telocéntricos y de los cromosomas bibraquiados. El presente estudio nos permite analizar un nuevo ejemplo de un polimorfismo robertsoniano. Los datos son discutidos en relación con la presencia de los polimorfismos robertsonianos en la naturaleza.

     

Chromosome multiformity in the genus Ctenomys (Rodentia,Octodontidae)

The karotypes of eleven species of the South American burrowing rodents, genus Ctenomys are described, and information on the somatic number of two other species of the same genus is given. The studied species are: C. torquatus (2n =68), C. tuconax (2n =61), C. minutus (2n=50), C. talarum (2n= 48), C. porteousi (2n=48), C. cf. minutus (2n=48), C. australis (2n=46), C. azarae (2n=48), C. latro (2n=42), C. magellanicus fueguinus (2n=36), C. tucumanus (2n=28), C. opimus luteolus (2n=26), and C. occultus (2n =22). This extreme intrageneric variation in somatic number is also reflected by a great amount of diversity in chromosome structure. Karyotypes seem to be rather constant at the species level. Autosomal polymorphism has been found in two of the species, namely C. talarum and C. latro. The hypothesis of the superimposition of Robertsoman rearrangements, pericentric inversions and translocations in the evolution of the karyotype of Ctenomys is advanced. The direction of chromosome change, either toward increase or decrease in chromosome number, is discussed. It is emphasized that high chromosome multiformity is correlated in Ctenomys with a rapid and explosive pattern of species diversification; the meaning of the small size of populations in enhancing the role of chromosome rearrangements in the evolution of Ctenomys is discussed.     

Arterial supply of the atrio-ventricular bundle and its right branch by the first diagonal artery: a dual vascularization

A case is described in which a septal artery originating from the first artery contributed to the vascular supply of the atrio-ventricular bundle, its right branch, the moderator band and the anterior papillary muscle of the right ventricle. Postmortem coronary angiograms and microdissection were use to determine the course of the arteries. The different patterns of origin of the anterior septal arteries were reviewed, and the role of these arteries as an anastomotic route in situations of proximal stenosis of the anterior interventricular artery is discussed.