排序方式: 共有49条查询结果,搜索用时 15 毫秒
21.
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities 总被引:2,自引:0,他引:2
Boyden LM Choi M Choate KA Nelson-Williams CJ Farhi A Toka HR Tikhonova IR Bjornson R Mane SM Colussi G Lebel M Gordon RD Semmekrot BA Poujol A Välimäki MJ De Ferrari ME Sanjad SA Gutkin M Karet FE Tucci JR Stockigt JR Keppler-Noreuil KM Porter CC Anand SK Whiteford ML Davis ID Dewar SB Bettinelli A Fadrowski JJ Belsha CW Hunley TE Nelson RD Trachtman H Cole TR Pinsk M Bockenhauer D Shenoy M Vaidyanathan P Foreman JW Rasoulpour M Thameem F Al-Shahrouri HZ Radhakrishnan J Gharavi AG Goilav B 《Nature》2012,482(7383):98-102
Hypertension affects one billion people and is a principal reversible risk factor for cardiovascular disease. Pseudohypoaldosteronism type II (PHAII), a rare Mendelian syndrome featuring hypertension, hyperkalaemia and metabolic acidosis, has revealed previously unrecognized physiology orchestrating the balance between renal salt reabsorption and K(+) and H(+) excretion. Here we used exome sequencing to identify mutations in kelch-like 3 (KLHL3) or cullin 3 (CUL3) in PHAII patients from 41 unrelated families. KLHL3 mutations are either recessive or dominant, whereas CUL3 mutations are dominant and predominantly de novo. CUL3 and BTB-domain-containing kelch proteins such as KLHL3 are components of cullin-RING E3 ligase complexes that ubiquitinate substrates bound to kelch propeller domains. Dominant KLHL3 mutations are clustered in short segments within the kelch propeller and BTB domains implicated in substrate and cullin binding, respectively. Diverse CUL3 mutations all result in skipping of exon 9, producing an in-frame deletion. Because dominant KLHL3 and CUL3 mutations both phenocopy recessive loss-of-function KLHL3 mutations, they may abrogate ubiquitination of KLHL3 substrates. Disease features are reversed by thiazide diuretics, which inhibit the Na-Cl cotransporter in the distal nephron of the kidney; KLHL3 and CUL3 are expressed in this location, suggesting a mechanistic link between KLHL3 and CUL3 mutations, increased Na-Cl reabsorption, and disease pathogenesis. These findings demonstrate the utility of exome sequencing in disease gene identification despite the combined complexities of locus heterogeneity, mixed models of transmission and frequent de novo mutation, and establish a fundamental role for KLHL3 and CUL3 in blood pressure, K(+) and pH homeostasis. 相似文献
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Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes 总被引:1,自引:0,他引:1
Endele S Rosenberger G Geider K Popp B Tamer C Stefanova I Milh M Kortüm F Fritsch A Pientka FK Hellenbroich Y Kalscheuer VM Kohlhase J Moog U Rappold G Rauch A Ropers HH von Spiczak S Tönnies H Villeneuve N Villard L Zabel B Zenker M Laube B Reis A Wieczorek D Van Maldergem L Kutsche K 《Nature genetics》2010,42(11):1021-1026
N-methyl-D-aspartate (NMDA) receptors mediate excitatory neurotransmission in the mammalian brain. Two glycine-binding NR1 subunits and two glutamate-binding NR2 subunits each form highly Ca2(+)-permeable cation channels which are blocked by extracellular Mg2(+) in a voltage-dependent manner. Either GRIN2B or GRIN2A, encoding the NMDA receptor subunits NR2B and NR2A, was found to be disrupted by chromosome translocation breakpoints in individuals with mental retardation and/or epilepsy. Sequencing of GRIN2B in 468 individuals with mental retardation revealed four de novo mutations: a frameshift, a missense and two splice-site mutations. In another cohort of 127 individuals with idiopathic epilepsy and/or mental retardation, we discovered a GRIN2A nonsense mutation in a three-generation family. In a girl with early-onset epileptic encephalopathy, we identified the de novo GRIN2A mutation c.1845C>A predicting the amino acid substitution p.N615K. Analysis of NR1-NR2A(N615K) (NR2A subunit with the p.N615K alteration) receptor currents revealed a loss of the Mg2(+) block and a decrease in Ca2(+) permeability. Our findings suggest that disturbances in the neuronal electrophysiological balance during development result in variable neurological phenotypes depending on which NR2 subunit of NMDA receptors is affected. 相似文献
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Opitz CA Litzenburger UM Sahm F Ott M Tritschler I Trump S Schumacher T Jestaedt L Schrenk D Weller M Jugold M Guillemin GJ Miller CL Lutz C Radlwimmer B Lehmann I von Deimling A Wick W Platten M 《Nature》2011,478(7368):197-203
Activation of the aryl hydrocarbon receptor (AHR) by environmental xenobiotic toxic chemicals, for instance 2,3,7,8-tetrachlorodibenzo-p-dioxin (dioxin), has been implicated in a variety of cellular processes such as embryogenesis, transformation, tumorigenesis and inflammation. But the identity of an endogenous ligand activating the AHR under physiological conditions in the absence of environmental toxic chemicals is still unknown. Here we identify the tryptophan (Trp) catabolite kynurenine (Kyn) as an endogenous ligand of the human AHR that is constitutively generated by human tumour cells via tryptophan-2,3-dioxygenase (TDO), a liver- and neuron-derived Trp-degrading enzyme not yet implicated in cancer biology. TDO-derived Kyn suppresses antitumour immune responses and promotes tumour-cell survival and motility through the AHR in an autocrine/paracrine fashion. The TDO-AHR pathway is active in human brain tumours and is associated with malignant progression and poor survival. Because Kyn is produced during cancer progression and inflammation in the local microenvironment in amounts sufficient for activating the human AHR, these results provide evidence for a previously unidentified pathophysiological function of the AHR with profound implications for cancer and immune biology. 相似文献
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COMPATIBLE EXTENSIONS OF FUZZY RELATIONS 总被引:1,自引:0,他引:1
Irina GEORGESCU 《系统科学与系统工程学报(英文版)》2003,12(3):332-349
In 1930 Szpilrajn proved that any strict partial order can be embedded in a strict linear order.This theorem was later refined by Dushnik and Miller(1941),Hansson(1968), Suzumura(1976),Donaldson and Weymark(1998), Bossert(1999). Particularly Suzumura introduced the important concept of compatible extension of a(crisp)relation.These extension theorems have an important role in welfare economics. In particularSzpilrajn theorem is the main tool for proving a known theorem of Richter that establishes theequivalence between rational and congruous consumers. In 1999 Duggan proved a general extensiontheorem that contains all these results. In this paper we introduce the notion of compatible extension of a fuzzy relation and we provean extension theorem for fuzzy relations. Our result generalizes to fuzzy set theory the main part ofDuggan's theorem. As applications we obtain fuzzy versions of the theorems of Szpilrajn, Hanssonand Suzumura. We also prove that an asymmetric and transitive fuzzy relation has a com 相似文献
26.
Pregnancy: a cloned horse born to its dam twin 总被引:1,自引:0,他引:1
Galli C Lagutina I Crotti G Colleoni S Turini P Ponderato N Duchi R Lazzari G 《Nature》2003,424(6949):635
Several animal species, including sheep, mice, cattle, goats, rabbits, cats, pigs and, more recently, mules have been reproduced by somatic cell cloning, with the offspring being a genetic copy of the animal donor of the nuclear material used for transfer into an enucleated oocyte. Here we use this technology to clone an adult horse and show that it is possible to establish a viable, full-term pregnancy in which the surrogate mother is also the nuclear donor. The cloned offspring is therefore genetically identical to the mare who carried it, challenging the idea that maternal immunological recognition of fetal antigens influences the well-being of the fetus and the outcome of the pregnancy. 相似文献
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Gharavi AG Kiryluk K Choi M Li Y Hou P Xie J Sanna-Cherchi S Men CJ Julian BA Wyatt RJ Novak J He JC Wang H Lv J Zhu L Wang W Wang Z Yasuno K Gunel M Mane S Umlauf S Tikhonova I Beerman I Savoldi S Magistroni R Ghiggeri GM Bodria M Lugani F Ravani P Ponticelli C Allegri L Boscutti G Frasca G Amore A Peruzzi L Coppo R Izzi C Viola BF Prati E Salvadori M Mignani R Gesualdo L Bertinetto F Mesiano P Amoroso A Scolari F Chen N Zhang H Lifton RP 《Nature genetics》2011,43(4):321-327
We carried out a genome-wide association study of IgA nephropathy, a major cause of kidney failure worldwide. We studied 1,194 cases and 902 controls of Chinese Han ancestry, with targeted follow up in Chinese and European cohorts comprising 1,950 cases and 1,920 controls. We identified three independent loci in the major histocompatibility complex, as well as a common deletion of CFHR1 and CFHR3 at chromosome 1q32 and a locus at chromosome 22q12 that each surpassed genome-wide significance (P values for association between 1.59 × 10?2? and 4.84 × 10?? and minor allele odds ratios of 0.63-0.80). These five loci explain 4-7% of the disease variance and up to a tenfold variation in interindividual risk. Many of the alleles that protect against IgA nephropathy impart increased risk for other autoimmune or infectious diseases, and IgA nephropathy risk allele frequencies closely parallel the variation in disease prevalence among Asian, European and African populations, suggesting complex selective pressures. 相似文献
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Amanda J. Wilson Roman Schoenauer Elisabeth Ehler Irina Agarkova Pauline M. Bennett 《Cellular and molecular life sciences : CMLS》2014,71(1):165-181
Cardiomyocytes grow during heart maturation or disease-related cardiac remodeling. We present evidence that the intercalated disc (ID) is integral to both longitudinal and lateral growth: increases in width are accommodated by lateral extension of the plicate tread regions and increases in length by sarcomere insertion within the ID. At the margin between myofibril and the folded membrane of the ID lies a transitional junction through which the thin filaments from the last sarcomere run to the ID membrane and it has been suggested that this junction acts as a proto Z-disc for sarcomere addition. In support of this hypothesis, we have investigated the ultrastructure of the ID in mouse hearts from control and dilated cardiomyopathy (DCM) models, the MLP-null and a cardiac-specific β-catenin mutant, cΔex3, as well as in human left ventricle from normal and DCM samples. We find that the ID amplitude can vary tenfold from 0.2 μm up to a maximum of ~2 μm allowing gradual expansion during heart growth. At the greatest amplitude, equivalent to a sarcomere length, A-bands and thick filaments are found within the ID membrane loops together with a Z-disc, which develops at the transitional junction position. Here, also, the tops of the membrane folds, which are rich in αII spectrin, become enlarged and associated with junctional sarcoplasmic reticulum. Systematically larger ID amplitudes are found in DCM samples. Other morphological differences between mouse DCM and normal hearts suggest that sarcomere inclusion is compromised in the diseased hearts. 相似文献
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Deciphering the evolution and metabolism of an anammox bacterium from a community genome 总被引:15,自引:0,他引:15
Strous M Pelletier E Mangenot S Rattei T Lehner A Taylor MW Horn M Daims H Bartol-Mavel D Wincker P Barbe V Fonknechten N Vallenet D Segurens B Schenowitz-Truong C Médigue C Collingro A Snel B Dutilh BE Op den Camp HJ van der Drift C Cirpus I van de Pas-Schoonen KT Harhangi HR van Niftrik L Schmid M Keltjens J van de Vossenberg J Kartal B Meier H Frishman D Huynen MA Mewes HW Weissenbach J Jetten MS Wagner M Le Paslier D 《Nature》2006,440(7085):790-794
Anaerobic ammonium oxidation (anammox) has become a main focus in oceanography and wastewater treatment. It is also the nitrogen cycle's major remaining biochemical enigma. Among its features, the occurrence of hydrazine as a free intermediate of catabolism, the biosynthesis of ladderane lipids and the role of cytoplasm differentiation are unique in biology. Here we use environmental genomics--the reconstruction of genomic data directly from the environment--to assemble the genome of the uncultured anammox bacterium Kuenenia stuttgartiensis from a complex bioreactor community. The genome data illuminate the evolutionary history of the Planctomycetes and allow us to expose the genetic blueprint of the organism's special properties. Most significantly, we identified candidate genes responsible for ladderane biosynthesis and biological hydrazine metabolism, and discovered unexpected metabolic versatility. 相似文献