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51.
Characterization of a new syndrome that associates craniosynostosis, delayed fontanel closure, parietal foramina, imperforate anus, and skin eruption: CDAGS 下载免费PDF全文
Mendoza-Londono R Lammer E Watson R Harper J Hatamochi A Hatamochi-Hayashi S Napierala D Hermanns P Collins S Roa BB Hedge MR Wakui K Nguyen D Stockton DW Lee B 《American journal of human genetics》2005,77(1):161-168
We describe the clinical characterization, molecular analyses, and genetic mapping of a distinct genetic condition characterized by craniosynostosis, delayed closure of the fontanel, cranial defects, clavicular hypoplasia, anal and genitourinary malformations, and skin eruption. We have identified seven patients with this phenotype in four families from different geographic regions and ethnic backgrounds. This is an autosomal recessive condition that brings together apparently opposing pathophysiologic and developmental processes, including accelerated suture closure and delayed ossification. Selected candidate genes--including RUNX2, CBFB, MSX2, ALX4, TWIST1, and RECQL4--were screened for mutations, by direct sequencing of their coding regions, and for microdeletions, by fluorescent in situ hybridization. No mutations or microdeletions were detected in any of the genes analyzed. A genomewide screen yielded the maximum estimated LOD score of +2.38 for markers D22S283 and D22S274 on chromosome 22q12-q13. We hypothesize that the gene defect in this condition causes novel context-dependent dysregulation of multiple signaling pathways, including RUNX2, during osteoblast differentiation and craniofacial morphogenesis. 相似文献
52.
Wilton R Yousef MA Saxena P Szpunar M Stevens FJ 《Protein expression and purification》2006,47(1):25-35
The receptor for advanced glycation endproducts (RAGE) is a multiligand receptor that binds a variety of structurally and functionally unrelated ligands, including advanced glycation endproducts (AGEs), amyloid fibrils, amphoterin, and members of the S100 family of proteins. The receptor has been implicated in the pathology of diabetes as well as in inflammatory processes and tumor cell metastasis. For the present study, the extracellular region of RAGE (exRAGE) was expressed as a soluble, C-terminal hexahistidine-tagged fusion protein in the periplasmic space of Escherichia coli. Proper processing and folding of the purified protein, predicted to contain three immunoglobulin-type domains, was supported by the results of electrospray mass spectroscopy and circular dichroism experiments. Sedimentation velocity experiments showed that exRAGE was primarily monomeric in solution. Binding to several RAGE ligands, including AGE-BSA, immunoglobulin light chain amyloid fibrils, and glycosaminoglycans, was demonstrated using pull-down, dot-blot, or enzyme-linked microplate assays. Using surface plasmon resonance, the interaction of exRAGE with AGE-BSA was shown to fit a two-site model, with KD values of 88 nM and 1.4 microM. The E. coli-derived exRAGE did not bind the advanced glycation endproduct Nepsilon-(carboxymethyl)lysine, as reported for the cellular receptor, and the possible role of RAGE glycosylation in recognition of this ligand is discussed. This new RAGE construct will facilitate detailed studies of RAGE-ligand interactions and provides a platform for preparation of site-directed mutants for future structure/function studies. 相似文献
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54.
Marzorati M Alma A Sacchi L Pajoro M Palermo S Brusetti L Raddadi N Balloi A Tedeschi R Clementi E Corona S Quaglino F Bianco PA Beninati T Bandi C Daffonchio D 《Applied and environmental microbiology》2006,72(2):1467-1475
Flavescence dorée (FD) is a grapevine disease that afflicts several wine production areas in Europe, from Portugal to Serbia. FD is caused by a bacterium, "Candidatus Phytoplasma vitis," which is spread throughout the vineyards by a leafhopper, Scaphoideus titanus (Cicadellidae). After collection of S. titanus specimens from FD-contaminated vineyards in three different areas in the Piedmont region of Italy, we performed a survey to characterize the bacterial microflora associated with this insect. Using length heterogeneity PCR with universal primers for bacteria we identified a major peak associated with almost all of the individuals examined (both males and females). Characterization by denaturing gradient gel electrophoresis confirmed the presence of a major band that, after sequencing, showed a 97 to 99% identity with Bacteroidetes symbionts of the "Candidatus Cardinium hertigii" group. In addition, electron microscopy of tissues of S. titanus fed for 3 months on phytoplasma-infected grapevine plants showed bacterial cells with the typical morphology of "Ca. Cardinium hertigii." This endosymbiont, tentatively designated ST1-C, was found in the cytoplasm of previtellogenic and vitellogenic ovarian cells, in the follicle cells, and in the fat body and salivary glands. In addition, cell morphologies resembling those of "Ca. Phytoplasma vitis" were detected in the midgut, and specific PCR assays indicated the presence of the phytoplasma in the gut, fat body and salivary glands. These results indicate that ST1-C and "Ca. Phytoplasma vitis" have a complex life cycle in the body of S. titanus and are colocalized in different organs and tissues. 相似文献
55.
Q Qi A Gibson X Fu M Zheng R Kuehn Y Wang Y Wang S Navarro JA Morrell D Jiang G Simmons E Bell NB Ivleva AL McClerren P Loida TG Ruff ME Petracek SB Preuss 《The Journal of biological chemistry》2012,287(37):31482-31493
Previous studies have demonstrated that Arabidopsis thaliana BBX32 (AtBBX32) represses light signaling in A. thaliana and that expression of AtBBX32 in soybean increases grain yield in multiple locations and multiyear field trials. The BBX32 protein is a member of the B-box zinc finger family from A. thaliana and contains a single conserved Zn(2+)-binding B-box domain at the N terminus. Although the B-box domain is predicted to be involved in protein-protein interactions, the mechanism of interaction is poorly understood. Here, we provide in vitro and in vivo evidence demonstrating the physical and functional interactions of AtBBX32 with another B-box protein, soybean BBX62 (GmBBX62). Deletion analysis and characterization of the purified B-box domain indicate that the N-terminal B-box region of AtBBX32 interacts with GmBBX62. Computational modeling and site-directed mutagenesis of the AtBBX32 B-box region identified specific residues as critical for mediating the interaction between AtBBX32 and GmBBX62. This study defines the plant B-box as a protein interaction domain and offers novel insight into its role in mediating specific protein-protein interactions between different plant B-box proteins. 相似文献
56.
Rosemarie Marchan Michaela S. Lesjak Joanna D. Stewart Roland Winter Janine Seeliger Jan G. Hengstler 《Cell cycle (Georgetown, Tex.)》2012,11(24):4499-4506
Recently, EDI3 was identified as a key factor for choline metabolism that controls tumor cell migration and is associated with metastasis in endometrial carcinomas. EDI3 cleaves glycerophosphocholine (GPC) to form choline and glycerol-3-phosphate (G3P). Choline is then further metabolized to phosphatidylcholine (PtdC), the major lipid in membranes and a key player in membrane-mediated cell signaling. The second product, G3P, is a precursor molecule for several lipids with central roles in signaling, for example lysophosphatidic acid (LPA), phosphatidic acid (PA) and diacylglycerol (DAG). LPA activates intracellular signaling pathways by binding to specific LPA receptors, including membrane-bound G protein-coupled receptors and the intracellular nuclear receptor, PPARγ. Conversely, PA and DAG mediate signaling by acting as lipid anchors that bind and activate several signaling proteins. For example, binding of GTPases and PKC to PA and DAG, respectively, increases the activation of signaling networks, mediating processes such as migration, adhesion, proliferation or anti-apoptosis—all relevant for tumor development. We present a concept by which EDI3 either directly generates signaling molecules or provides “membrane anchors” for downstream signaling factors. As a result, EDI3 links choline metabolism to signaling activities resulting in a more malignant phenotype. 相似文献
57.
Summary A new section through Cretaceous deposits was discovered 1 km west of the Dizlu village (approximately 40 km north of Esfahan,
central Iran). Lithologically, the section distinctly differs from all other sections exposed in neighboring localities. A
scleractinian coral fauna (Upper Aptian-Upper Albian), collected from a reefal limestone, is described in detail. The following
taxa were found:Actinastrea aff.pseudominima (Koby),Columactinastraea sp.,Eugyra cotteaui (d'Orbigny),Pseudomyriophyllia turnsekae Baron-Szabo,Montlivaltia sp.,Paraclausastrea pulchra Morycowa,Placocoenia robusta Oppenheim,Columnocoenia ksiazkiewiczi Morycowa,Stylina micropora Koby,Felixigyra deangelisi Prever,Cyathophora haysensis Wells,Diploastraea harrisi Wells,Morphastrea cf.ludovicina (Michelin),Meandrophyllia meandroides (Koby),Eocomoseris raueni L?ser,Fungiastrea crespoi (Felix),Latiastraea cf.kaufmanni (Koby),Kobya aff.crassolamellosa Gregory. The coral association of the Esfahan region is dominated by forms that are known to be cosmopolitan and semicosmopolitan
in the Lower Cretaceous. It was found that over 40% of the coral fauna had previously been reported from both Lower and Upper
Cretaceous strata. A similar pattern has been recognized for other reefal associations (e.g. Albian of Greece and Upper Barremian-Middle
Albian of Mexico). In contrast, coral assemblages which developed in rather soft bottom environments have a significantly
smaller percentage (15–20%) of taxa extending into the Upper Cretaceous and show closer affinities to Upper Jurassic and Lower
Cretaceous faunas. 相似文献
58.
Rosemarie?W.?HammondEmail author 《In vitro cellular & developmental biology. Plant》2005,41(4):405-410
Summary The study of plant viruses and their interaction with the plant host has contributed greatly to our understanding of plant
biology. The recent development of plant viruses as transient expression vectors has not only enhanced our understanding of
virus biology and antiviral defense mechanisms in plants, but has also led to the use of plant viral-based vectors as tools
for gene discovery and production of recombinant proteins in plants for control of human and animal diseases. An overview
of the state-of-the-art of viral expression systems, is presented, as well as examples from our laboratory on their use in
identifying nuclear targeting motifs on viroid molecules and development of therapeutic proteins for control of animal diseases. 相似文献
59.
Lee HH Meyer EH Goya S Pichavant M Kim HY Bu X Umetsu SE Jones JC Savage PB Iwakura Y Casasnovas JM Kaplan G Freeman GJ DeKruyff RH Umetsu DT 《Journal of immunology (Baltimore, Md. : 1950)》2010,185(9):5225-5235
T cell Ig-like mucin-like-1 (TIM-1) is an important asthma susceptibility gene, but the immunological mechanisms by which TIM-1 functions remain uncertain. TIM-1 is also a receptor for phosphatidylserine (PtdSer), an important marker of cells undergoing programmed cell death, or apoptosis. We now demonstrate that NKT cells constitutively express TIM-1 and become activated by apoptotic cells expressing PtdSer. TIM-1 recognition of PtdSer induced NKT cell activation, proliferation, and cytokine production. Moreover, the induction of apoptosis in airway epithelial cells activated pulmonary NKT cells and unexpectedly resulted in airway hyperreactivity, a cardinal feature of asthma, in an NKT cell-dependent and TIM-1-dependent fashion. These results suggest that TIM-1 serves as a pattern recognition receptor on NKT cells that senses PtdSer on apoptotic cells as a damage-associated molecular pattern. Furthermore, these results provide evidence for a novel innate pathway that results in airway hyperreactivity and may help to explain how TIM-1 and NKT cells regulate asthma. 相似文献
60.
Phosphorylation of solubilized and purified high-affinity (Ca2+ + Mg2+)-ATPase (ATP phosphohydrolase, EC 3.6.1.3) of human erythrocyte membranes shows no dependence on cyclic AMP concentration in the range 0.1–1000 μM.Ca2+-dependent phosphoprotein is sensitive to hydroxylamine and molybdate treatment. The phosphate linkage shows maximum stability at low pH values, which is progressively lost as the pH rises, with a shoulder around pH 6. SDS gel electrophoresis of the phosphorylated protein yields a peak which shows relative mobility corresponding to a molecular weight of 145 000 and sensitivity to MgATP-chase and hydroxylamine treatment. This indicates that the phosphoprotein represents the phosphorylated intermediate of the high-affinity (Ca2+ + Mg2+)-ATPase of human erythrocyte membranes. 相似文献