Berry abscission is related to berry growth in Vitis labruscana 'Concord' and Vitis vinifera 'Riesling'

Research Note

Effects of the whole vine versus single shoot-crop level on fruit growth in Vitis labruscana 'Concord'

The fruit growth response to the whole vine and single shoot crop level was studied in Vitis labruscana 'Concord' grown in the North-Eastern United States. In vines thinned to lower and higher yields (equivalent to 12 and 21 t·ha-1), different number of clusters per shoot were retained after cluster thinning one week after set. Results showed that the seasonal accumulation of berry dry weight, fruit fresh weight, and the berry total soluble solids at harvest were only affected by the whole vine crop level. This suggests that under the conditions of this experiment shoots are not autonomous in terms of carbon partitioning to the fruit. Hence, crop level effects on fruit development can be considered and modelled on a whole vine basis.

The effects of pre- and post-veraison water stress on growth and physiology of potted Pinot Noir grapevines at varying crop levels

The interactions of water stress timing and crop level on growth, gas exchange, water relations and ripening of potted Pinot Noir grapevines were examined. Pre-veraison water stress induced a greater reduction of shoot and berry growth and a more rapid limitation of net photosynthesis (Pn) and stomatal conductance (g(s)) as compared to post-veraison stress. At the end of stress, when mid-day and pre-dawn leaf water potential were below -1.1 and -0.6 MPa, the reduction in Pn of stressed vines was more marked in the 2- and 4-cluster plants versus 1-cluster plant. Crop level had almost no significant effects on gas-exchange, growth and ripening and but few interactions with timing of water stress. These responses seem to reflect the high leaf area-to-fruit ratios at each crop level which probably buffered the effects of reduced leaf function induced by water stress

Laser scanning estimation of relative light interception by canopy components in different grapevine training systems

The fractional light interception by different parts of vines trained to various systems was estimated by a modified point-quadrat method using an over-row solar are positioning device equipped with a laser to simulate sunbeam position and angle at any latitude and time of the day. Laser readings were also combined with total vine light interception estimates via a line sensor to calculate the total light intercepted by specific canopy components. At each sampling date (late June and September, corresponding to fruit set and full canopy), type and position of organs were directly detected by the laser beam. Regardless of sampling date, the relative amount of light captured by the renewal-fruiting area (nodes 1 to 6) of simple cordon (SC) and double curtain (GDC) was considerably higher than that of spur-pruned cordon (SPC), whose vegetative area (distal to node 6) received about two-thirds of the incoming light. Relative light interception by main and lateral leaves was rather constant for GDC, thus reflecting the negligible regrowth after topping. By contrast, SC and SPC showed a much stronger response to topping which caused an increase of light interception by laterals (19 % for SC and +21 % for SPC). Frequencies of relative intercepted light by main leaves as a function of node position showed a peak around nodes 6-8, a zone where maximum leaf size is attained in all systems and on all dates. Instead, lateral leaves predominantly exposed to light were within the three basal nodes of the lateral shoots. Estimates of relative and total light for different vine parts at any time during the season as detected by laser scanning can objectively assess important characteristics of grapevine training systems, e.g. cluster and basal node exposure to light

FLPe functions in zebrafish embryos

To assay the efficiency of the FLP/FRT site-specific recombination system in Danio rerio, a construct consisting of a muscle-specific promoter driving EGFP flanked by FRT sites was developed. FLPe capped RNA was microinjected into transgenic single cell stage zebrafish embryos obtained by crossing hemizygous transgenic males with wild-type females. By 48 h post fertilization (hpf), the proportion of embryos displaying green fluorescence following FLPe RNA microinjection was significantly lower (7.7%; P < 0.001) than would be expected from a cross in the absence of the recombinase (50%). Embryos that retained fluorescence displayed marked mosaicism. Inheritance of the excised transgene in non-fluorescent, transgenic embryos was verified by PCR analysis and FLPe-mediated recombination was confirmed by DNA sequencing. Sperm derived from confirmed transgenic males in these experiments was used to fertilize wild-type eggs to determine whether germline excision of the transgene had occurred. Clutches sired by FLPe-microinjected males contained 0–4% fluorescent embryos. Transgenic males that were phenotypically wild-type produced no fluorescent progeny, demonstrating complete excision of the transgene from their germline. FLPe microinjected males that retained some fluorescent muscle expression produced a small proportion of fluorescent offspring, suggesting that in mosaic males not all germline cells had undergone FLPe-mediated transgene excision. Our results show that FLPe, which is derived from Saccharomyces cerevisiae, is an efficient recombinase in zebrafish maintained at 28.5°C

Ezrin Is Highly Expressed in Early Thymocytes, but Dispensable for T Cell Development in Mice

Ezrin/radixin/moesin (ERM) proteins are highly homologous proteins that function to link cargo molecules to the actin cytoskeleton. Ezrin and moesin are both expressed in mature lymphocytes, where they play overlapping roles in cell signaling and polarity, but their role in lymphoid development has not been explored.We characterized ERM protein expression in lymphoid tissues and analyzed the requirement for ezrin expression in lymphoid development. In wildtype mice, we found that most cells in the spleen and thymus express both ezrin and moesin, but little radixin. ERM protein expression in the thymus was differentially regulated, such that ezrin expression was highest in immature thymocytes and diminished during T cell development. In contrast, moesin expression was low in early thymocytes and upregulated during T cell development. Mice bearing a germline deletion of ezrin exhibited profound defects in the size and cellularity of the spleen and thymus, abnormal thymic architecture, diminished hematopoiesis, and increased proportions of granulocytic precursors. Further analysis using fetal liver chimeras and thymic transplants showed that ezrin expression is dispensable in hematopoietic and stromal lineages, and that most of the defects in lymphoid development in ezrin(-/-) mice likely arise as a consequence of nutritional stress.We conclude that despite high expression in lymphoid precursor cells, ezrin is dispensable for lymphoid development, most likely due to redundancy with moesin

The Development of Mouse APECED Models Provides New Insight into the Role of AIRE in Immune Regulation

Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy is a rare recessive autoimmune disorder caused by a defect in a single gene called AIRE (autoimmune regulator). Characteristics of this disease include a variable combination of autoimmune endocrine tissue destruction, mucocutaneous candidiasis and ectodermal dystrophies. The development of Aire-knockout mice has provided an invaluable model for the study of this disease. The aim of this review is to briefly highlight the strides made in APECED research using these transgenic murine models, with a focus on known roles of Aire in autoimmunity. The findings thus far are compelling and prompt additional areas of study which are discussed

Fstl1 Antagonizes BMP Signaling and Regulates Ureter Development

Bone morphogenetic protein (BMP) signaling pathway plays important roles in urinary tract development although the detailed regulation of its activity in this process remains unclear. Here we report that follistatin-like 1 (Fstl1), encoding a secreted extracellular glycoprotein, is expressed in developing ureter and antagonizes BMP signaling activity. Mouse embryos carrying disrupted Fstl1 gene displayed prominent hydroureter arising from proximal segment and ureterovesical junction defects. These defects were associated with significant reduction in ureteric epithelial cell proliferation at E15.5 and E16.5 as well as absence of subepithelial ureteral mesenchymal cells in the urinary tract at E16.5 and E18.5. At the molecular level, increased BMP signaling was found in Fstl1 deficient ureters, indicated by elevated pSmad1/5/8 activity. In vitro study also indicated that Fstl1 can directly bind to ALK6 which is specifically expressed in ureteric epithelial cells in developing ureter. Furthermore, Sonic hedgehog (SHH) signaling, which is crucial for differentiation of ureteral subepithelial cell proliferation, was also impaired in Fstl1-/- ureter. Altogether, our data suggest that Fstl1 is essential in maintaining normal ureter development by antagonizing BMP signaling

The BMP Antagonist Follistatin-Like 1 Is Required for Skeletal and Lung Organogenesis

Follistatin-like 1 (Fstl1) is a secreted protein of the BMP inhibitor class. During development, expression of Fstl1 is already found in cleavage stage embryos and becomes gradually restricted to mesenchymal elements of most organs during subsequent development. Knock down experiments in chicken and zebrafish demonstrated a role as a BMP antagonist in early development. To investigate the role of Fstl1 during mouse development, a conditional Fstl1 KO allele as well as a Fstl1-GFP reporter mouse were created. KO mice die at birth from respiratory distress and show multiple defects in lung development. Also, skeletal development is affected. Endochondral bone development, limb patterning as well as patterning of the axial skeleton are perturbed in the absence of Fstl1. Taken together, these observations show that Fstl1 is a crucial regulator in BMP signalling during mouse development

Plxdc2 Is a Mitogen for Neural Progenitors

The development of different brain regions involves the coordinated control of proliferation and cell fate specification along and across the neuraxis. Here, we identify Plxdc2 as a novel regulator of these processes, using in ovo electroporation and in vitro cultures of mammalian cells. Plxdc2 is a type I transmembrane protein with some homology to nidogen and to plexins. It is expressed in a highly discrete and dynamic pattern in the developing nervous system, with prominent expression in various patterning centres. In the chick neural tube, where Plxdc2 expression parallels that seen in the mouse, misexpression of Plxdc2 increases proliferation and alters patterns of neurogenesis, resulting in neural tube thickening at early stages. Expression of the Plxdc2 extracellular domain alone, which can be cleaved and shed in vivo, is sufficient for this activity, demonstrating a cell non-autonomous function. Induction of proliferation is also observed in cultured embryonic neuroepithelial cells (ENCs) derived from E9.5 mouse neural tube, which express a Plxdc2-binding activity. These experiments uncover a direct molecular activity of Plxdc2 in the control of proliferation, of relevance in understanding the role of this protein in various cancers, where its expression has been shown to be altered. They also implicate Plxdc2 as a novel component of the network of signalling molecules known to coordinate proliferation and differentiation in the developing nervous system