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391.
Alon Margalit Avinoam A. Livne Jørgen Funder Yosef Granot 《The Journal of membrane biology》1993,136(3):303-311
Platelets revert hypotonic-induced swelling by the process of regulatory volume decrease (RVD). We have recently shown that this process is under the control of endogenous hepoxilin A3. In this work, we investigated the mechanical-biochemical transduction that leads to hepoxilin A3 formation. We demonstrate that this process is mediated by pertussis-toxin-sensitive G protein, which activates Ca2+-insensitive phospholipase A2, and the sequential release of arachidonic acid. This conclusion is supported by the following observations: (i) RVD response is blocked selectively by the phospholipase A2 inhibitors manoalide and bromophenacyl-bromide (0.2 and 5
m, respectively) but not by phospholipase C inhibitors. The addition of arachidonic acid overcame this inhibition; (ii) extracellular Ca2+ depletion by EGTA (up to 10 mm) does not affect RVD; (iii) intracellular Ca2+ depletion by BAPTAAM (100
m) inhibits RVD but not hepoxilin A3 formation, as tested by the RVD reconstitution assay; (iv) RVD is inhibited by the G-protein inhibitors, GDP
S (1
m) and pertussis toxin (1 ng/ml). This inhibition is overcome by addition of arachidonic acid or hypotonic cell-free eluate that contains hepoxilin A3; (v) NaF, 1 mm, induces hepoxilin A3 formation, tested by the RVD reconstitution assay; and (vii) GDP
S inhibits hepoxilin A3 formation associated with flow. Therefore, it seems that G proteins are involved in the initial step of the mechanical-biochemical transduction leading to hepoxilin A3 formation in human platelets.DeceasedThis work is dedicated to the memory of Prof. A.A. Livne. It was carried out at the Amelia (Mimi) Rose Laboratory for Cellular Signal Transduction at the Department of Life Sciences, Ben-Gurion University of the Negev. We thank A. Dannon for helpful discussion. 相似文献
392.
Giovanni Blandino Francesco Fazi Sara Donzelli Merav Kedmi Aldema Sas-Chen Paola Muti Sabrina Strano Yosef Yarden 《FEBS letters》2014
Tumor initiation and progression are the outcomes of a stepwise accumulation of genetic alterations. Among these, gene amplification and aberrant expression of oncogenic proteins, as well as deletion or inactivation of tumor suppressor genes, represent hallmark steps. Mounting evidence collected over the last few years has identified different populations of non-coding RNAs as major players in tumor suppression in almost all cancer types. Elucidating the diverse molecular mechanisms underlying the roles of non-coding RNAs in tumor progression might provide illuminating insights, potentially able to assist improved diagnosis, better staging and effective treatments of human cancers. Here we focus on several groups of tumor suppressor microRNAs, whose downregulation exerts a profound oncologic impact and might be harnessed for the benefit of cancer patients. 相似文献
393.
The relationship between chlorophyll a (Chl a) and primary productivity(PP) in the uppermost water layer and the water column-based(015 m) integral values of those variables were examinedusing measurements taken in Lake Kinneret (Israel) from 1990to 2003. In 81% of all Chl a profiles examined, the distributionwas fairly uniform within the entire 015 m water column,and 12.3% of instances showed a prominent subsurface maximum,when the lake phytoplankton was dominated by the dinoflagellatePeridinium gatunense. Chl a can be reliably estimated by remotesensing techniques in the productive and turbid water of LakeKinneret, since Chl a concentration at surface layers can beextrapolated to the entire water column. Light vertical attenuationcoefficient average for wavelengths from 400 to 700 nm, Kd,ranged from 0.203 to 1.954 m1 and showed high degreeof temporal variation. The maximal rate of photosynthetic efficiency,PBopt [average 3.16 (±1.50)], ranged from 0.25 to 8.85mg C m3 h1 mg Chl a1. Using measured dataof Chl a, PBopt, and light as an input, a simple depth-integratedPP model allowed plausible simulation of PP. However, a lackof correlation between photosynthetic activity and temperature(or other variable with remotely sensed potential) renders theuse of models that require input of photosynthetic efficiencyto calculate integrated PP of little value in the case of productiveand turbid Lake Kinneret. 相似文献
394.
We have developed a simple method for single-step cloning of any PCR product into a plasmid. A novel selection principle has been applied, in which activation of a drug selection marker is achieved following homologous recombination. In this method a DNA fragment is amplified by PCR with standard oligonucleotides that contain flanking tails derived from the host plasmid and the complete λPR or rrnA1 promoter regions. The resulting PCR product is then electroporated into an Escherichia coli strain harboring both the phage λ Red functions and the host plasmid. Upon homologous recombination of the PCR fragment into the plasmid, expression of a drug selection marker is fully induced due to restoration of its truncated promoter, thus allowing appropriate selection. Recombinant plasmid vectors encoding β-galactosidase and neomycin phosphotransferase were constructed by using this method in two well-known Red systems. This cloning strategy significantly reduces both the time and costs associated with cloning procedures. 相似文献
395.
Edward Avezov Efrat Ron Yana Izenshtein Yosef Adan Gerardo Z. Lederkremer 《Journal of visualized experiments : JoVE》2010,(38)
Attachment of the Glc3Man9GlcNAc2 precursor oligosaccharide to nascent polypeptides in the ER is a common modification for secretory proteins. Although this modification was implicated in several biological processes, additional aspects of its function are emerging, with recent evidence of its role in the production of signals for glycoprotein quality control and trafficking. Thus, phenomena related to N-linked glycans and their processing are being intensively investigated. Methods that have been recently developed for proteomic analysis have greatly improved the characterization of glycoprotein N-linked glycans. Nevertheless, they do not provide insight into the dynamics of the sugar chain processing involved. For this, labeling and pulse-chase analysis protocols are used that are usually complex and give very low yields. We describe here a simple method for the isolation and analysis of metabolically labeled N-linked oligosaccharides. The protocol is based on labeling of cells with [2-3H] mannose, denaturing lysis and enzymatic release of the oligosaccharides from either a specifically immunoprecipitated protein of interest or from the general glycoprotein pool by sequential treatments with endo H and N-glycosidase F, followed by molecular filtration (Amicon). In this method the isolated oligosaccharides serve as an input for HPLC analysis, which allows discrimination between various glycan structures according to the number of monosaccharide units comprising them, with a resolution of a single monosaccharide. Using this method we were able to study high mannose N-linked oligosaccharide profiles of total cell glycoproteins after pulse-chase in normal conditions and under proteasome inhibition. These profiles were compared to those obtained from an immunoprecipitated ER-associated degradation (ERAD) substrate. Our results suggest that most NIH 3T3 cellular glycoproteins are relatively stable and that most of their oligosaccharides are trimmed to Man9-8GlcNAc2. In contrast, unstable ERAD substrates are trimmed to Man6-5GlcNAc2 and glycoproteins bearing these species accumulate upon inhibition of proteasomal degradation.Download video file.(118M, mp4) 相似文献
396.
Yosef Shiloh Gilad Litvak Yael Ziv Thomas Lehner Lodewijk Sandkuyl Minka Hildesheimer Vered Buchris Frans P. M. Cremers Paul Szabo Bradley N. White Jeanette J. A. Holden Jurg Ott 《American journal of human genetics》1990,47(1):20-27
X-linked albinism-deafness syndrome (ADFN) was described in one Israeli Jewish family and is characterized by congenital nerve deafness and piebaldness. The ADFN mutation probably affects the migration of neural crest-derived precursors of the melanocytes. As a first step toward identifying the ADFN gene, a linkage study was performed to localize the disease locus on the X chromosome. The family was found to be informative for 11 of 107 RFLPs along the X, and two-point analysis showed four of them--factor 9 (F9), DXS91, DXS37, and DNF1--to have definite or suggestive linkage with ADFN. Multipoint linkage analysis indicated two possible orders within this cluster of loci, neither of which was preferable. In both orders F9 was the most distal, and the best estimate for the location of ADFN was between F9 and the next proximal marker (8.6 cM from F9 [Z = 8.1] or 8.3 cM from F9 [Z = 7.9]). These results suggest that the ADFN is at Xq26.3-q27.1. Disagreement between our data and previous localization of DXS91 at Xq11-q13 was resolved by hybridization of the probe pXG-17, which detects the DXS91 locus, to a panel of somatic cell hybrids containing different portions of the X chromosome. This experiment showed that this locus is definitely at Xq24-q26. Together with the linkage data, our results place DXS91 at Xq26 and underscore the importance of using more than one mapping method for the localization of molecular probes. 相似文献
397.
398.
Ron D. Jachimowicz Filippo Beleggia Jörg Isensee Bhagya Bhavana Velpula Jonas Goergens Matias A. Bustos Markus A. Doll Anjana Shenoy Cintia Checa-Rodriguez Janica Lea Wiederstein Keren Baranes-Bachar Christoph Bartenhagen Falk Hertwig Nizan Teper Tomohiko Nishi Anna Schmitt Felix Distelmaier Hermann-Josef Lüdecke Yosef Shiloh 《Cell》2019,176(3):505-519.e22
399.
Stanislav Pen-Mouratov Salvador Rodriguez-Zaragoza Yosef Steinberger 《Ecological Research》2008,23(6):973-982
Vegetation cover is known to act as an abiotic mediator influencing the structure of soil fauna communities in arid and semi-arid
ecosystems. The aim of the current research was to determine the spatial dispersion of the soil free-living nematode community
under the canopy of Cercidium praecox and Prosopis laevigata during the rainy season. These shrubs are the dominant plant associations in the western part of the Tehuacán-Cuicatlán Valley
in Mexico. Soil samples were taken from each 10-cm depth between 0 and 50 cm in August 2004. Our results demonstrated that
the abundance and structure of the soil free-living nematode communities in the study area were strongly dependent on plant
effects, specified by limited factors such as soil moisture and organic matter availability. The greatest degree of abundance
of soil-free-living nematodes (88%) was found in the upper (0–10 cm) soil layer. Plant parasites were the most abundant trophic
group under the two plants (58 and 36% under Parkinsonia (Cercidium) praecox and Prosopis laevigata, respectively), whereas omnivore-predators were the most dominant (96%) in inter-plant spaces. The fungivore/bacterivore
(F/B) ratio was found to be the most useful tool of the ecological indices tested in the present study, reflecting the vertical
distribution of the free-living nematode communities beneath different plant species in the different soil layers. The soil
free-living nematode communities and their vertical distribution were found to be affected by plant ecophysiological adaptation,
soil moisture, and the interaction between them. 相似文献
400.
Katz M Shtiegman K Tal-Or P Yakir L Mosesson Y Harari D Machluf Y Asao H Jovin T Sugamura K Yarden Y 《Traffic (Copenhagen, Denmark)》2002,3(10):740-751
Ligand-dependent endocytosis of the epidermal growth factor receptor (EGFR) involves recruitment of a ubiquitin ligase, and sorting of ubiquitylated receptors to lysosomal degradation. By studying Hgs, a mammalian homolog of a yeast vacuolar-sorting adaptor, we provide information on the less understood, ligand-independent pathway of receptor endocytosis and degradation. Constitutive endocytosis involves receptor ubiquitylation and translocation to Hgs-containing endosomes. Whereas the lipid-binding motif of Hgs is necessary for receptor endocytosis, the ubiquitin-interacting motif negatively regulates receptor degradation. We demonstrate that the ubiquitin-interacting motif is endowed with two functions: it binds ubiquitylated proteins and it targets self-ubiquitylation by recruiting Nedd4, an ubiquitin ligase previously implicated in endocytosis. Based upon the dual function of the ubiquitin-interacting motif and its wide occurrence in endocytic adaptors, we propose a ubiquitin-interacting motif network that relays ubiquitylated membrane receptors to lysosomal degradation through successive budding events. 相似文献