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31.
Pennacchio LA Ahituv N Moses AM Prabhakar S Nobrega MA Shoukry M Minovitsky S Dubchak I Holt A Lewis KD Plajzer-Frick I Akiyama J De Val S Afzal V Black BL Couronne O Eisen MB Visel A Rubin EM 《Nature》2006,444(7118):499-502
Identifying the sequences that direct the spatial and temporal expression of genes and defining their function in vivo remains a significant challenge in the annotation of vertebrate genomes. One major obstacle is the lack of experimentally validated training sets. In this study, we made use of extreme evolutionary sequence conservation as a filter to identify putative gene regulatory elements, and characterized the in vivo enhancer activity of a large group of non-coding elements in the human genome that are conserved in human-pufferfish, Takifugu (Fugu) rubripes, or ultraconserved in human-mouse-rat. We tested 167 of these extremely conserved sequences in a transgenic mouse enhancer assay. Here we report that 45% of these sequences functioned reproducibly as tissue-specific enhancers of gene expression at embryonic day 11.5. While directing expression in a broad range of anatomical structures in the embryo, the majority of the 75 enhancers directed expression to various regions of the developing nervous system. We identified sequence signatures enriched in a subset of these elements that targeted forebrain expression, and used these features to rank all approximately 3,100 non-coding elements in the human genome that are conserved between human and Fugu. The testing of the top predictions in transgenic mice resulted in a threefold enrichment for sequences with forebrain enhancer activity. These data dramatically expand the catalogue of human gene enhancers that have been characterized in vivo, and illustrate the utility of such training sets for a variety of biological applications, including decoding the regulatory vocabulary of the human genome. 相似文献
32.
R. Velasco Alonso J. Prieto Valtuena M. A. del Pozzo Perez M. I. Gonzales Guilabert L. Corporales Lopez 《Cellular and molecular life sciences : CMLS》1973,29(7):870-871
Resumen Se ha estudiado la relación existente entre la concentración de Ig. sericas y las poblaciones linfocitarias T y B en un grupo de sujetos ancianos, encontrandose un notable descenso de la transformación blasticá al tiempo que se incrementa el porcentage de linfocitos portadores de Ig. en su membrana. De nuestros resultados parece deducirse una relación entre el nivel de Ig. sericas y la población medulo-derivada. 相似文献
33.
Microtubule associated protein tau binds to double-stranded but not single-stranded DNA 总被引:3,自引:0,他引:3
Hua Q He RQ Haque N Qu MH del Carmen Alonso A Grundke-Iqbal I Iqbal K 《Cellular and molecular life sciences : CMLS》2003,60(2):413-421
Tau, a major microtubule-associated protein of the neuron, which is known to promote the assembly of and to stabilize microtubules,
has also been seen associated with chromatin in neuronal cell lines, but its role in this subcellular compartment is still
unknown. In this study, the binding of tau to DNA was investigated using the electrophoretic mobility shift assay. Using polynucleotide
as probe, we found that tau bound to double-stranded but not to single-stranded DNA. Formation of tau-polynucleotide complex
was disrupted by alkaline pH and a high concentration of NaCl, but was not affected by dithiothreitol. Electron microscopy
revealed that the protein associated with the nucleic acid in a necklacelike manner. DNA-cellulose chromatography and radioimmunodot-blot
analyses showed that calf thymus histones VI-S, VII-S and VIII-S could replace both recombinant human brain tau352 (tau-23) and tau441 (tau-40) from DNA. Thus, tau appears to bind to DNA reversibly in the presence of histones.
Received 24 November 2002; received after revision 28 December 2002; accepted 30 December 2002
RID="*"
ID="*"Corresponding author. 相似文献
34.
Mira MT Alcaïs A Van Thuc N Thai VH Huong NT Ba NN Verner A Hudson TJ Abel L Schurr E 《Nature genetics》2003,33(3):412-415
Leprosy, a chronic infectious disease caused by Mycobacterium leprae, affects an estimated 700,000 persons each year. Clinically, leprosy can be categorized as paucibacillary or multibacillary disease. These clinical forms develop in persons that are intrinsically susceptible to leprosy per se, that is, leprosy independent of its specific clinical manifestation. We report here on a genome-wide search for loci controlling susceptibility to leprosy per se in a panel of 86 families including 205 siblings affected with leprosy from Southern Vietnam. Using model-free linkage analysis, we found significant evidence for a susceptibility gene on chromosome region 6q25 (maximum likelihood binomial (MLB) lod score 4.31; P = 5 x 10(-6)). We confirmed this by family-based association analysis in an independent panel of 208 Vietnamese leprosy simplex families. Of seven microsatellite markers underlying the linkage peak, alleles of two markers (D6S1035 and D6S305) showed strong evidence for association with leprosy (P = 6.7 x 10(-4) and P = 5.9 x 10(-5), respectively). 相似文献
35.
Tony Van Gestel Marcelo Espinoza Bart Baesens Johan A. K. Suykens Carine Brasseur Bart De Moor 《Journal of forecasting》2006,25(2):77-100
The use of linear error correction models based on stationarity and cointegration analysis, typically estimated with least squares regression, is a common technique for financial time series prediction. In this paper, the same formulation is extended to a nonlinear error correction model using the idea of a kernel‐based implicit nonlinear mapping to a high‐dimensional feature space in which linear model formulations are specified. Practical expressions for the nonlinear regression are obtained in terms of the positive definite kernel function by solving a linear system. The nonlinear least squares support vector machine model is designed within the Bayesian evidence framework that allows us to find appropriate trade‐offs between model complexity and in‐sample model accuracy. From straightforward primal–dual reasoning, the Bayesian framework allows us to derive error bars on the prediction in a similar way as for linear models and to perform hyperparameter and input selection. Starting from the results of the linear modelling analysis, the Bayesian kernel‐based prediction is successfully applied to out‐of‐sample prediction of an aggregated equity price index for the European chemical sector. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
36.
37.
The functional importance of the roughly 98% of mammalian genomes not corresponding to protein coding sequences remains largely undetermined. Here we show that some large-scale deletions of the non-coding DNA referred to as gene deserts can be well tolerated by an organism. We deleted two large non-coding intervals, 1,511 kilobases and 845 kilobases in length, from the mouse genome. Viable mice homozygous for the deletions were generated and were indistinguishable from wild-type littermates with regard to morphology, reproductive fitness, growth, longevity and a variety of parameters assaying general homeostasis. Further detailed analysis of the expression of multiple genes bracketing the deletions revealed only minor expression differences in homozygous deletion and wild-type mice. Together, the two deleted segments harbour 1,243 non-coding sequences conserved between humans and rodents (more than 100 base pairs, 70% identity). Some of the deleted sequences might encode for functions unidentified in our screen; nonetheless, these studies further support the existence of potentially 'disposable DNA' in the genomes of mammals. 相似文献
38.
Mira MT Alcaïs A Nguyen VT Moraes MO Di Flumeri C Vu HT Mai CP Nguyen TH Nguyen NB Pham XK Sarno EN Alter A Montpetit A Moraes ME Moraes JR Doré C Gallant CJ Lepage P Verner A Van De Vosse E Hudson TJ Abel L Schurr E 《Nature》2004,427(6975):636-640
Leprosy is caused by Mycobacterium leprae and affects about 700,000 individuals each year. It has long been thought that leprosy has a strong genetic component, and recently we mapped a leprosy susceptibility locus to chromosome 6 region q25-q26 (ref. 3). Here we investigate this region further by using a systematic association scan of the chromosomal interval most likely to harbour this leprosy susceptibility locus. In 197 Vietnamese families we found a significant association between leprosy and 17 markers located in a block of approx. 80 kilobases overlapping the 5' regulatory region shared by the Parkinson's disease gene PARK2 and the co-regulated gene PACRG. Possession of as few as two of the 17 risk alleles was highly predictive of leprosy. This was confirmed in a sample of 975 unrelated leprosy cases and controls from Brazil in whom the same alleles were strongly associated with leprosy. Variants in the regulatory region shared by PARK2 and PACRG therefore act as common risk factors for leprosy. 相似文献
39.
Marcelo Fernandes 《Journal of forecasting》1998,17(7):497-514
The conditional heteroscedastic models (CHM) are commonly used to describe the dynamics of nominal exchange rates. However, some investigations have already pointed out that the CHMs are not able to fully explain all non-linearities exhibited by the exchange rate series. This paper analyses the performance of univariate CHMs in modelling the non-linearities of nominal exchange rate series vis-à-vis the US dollar. Twelve currencies are examined on a weekly basis: The Belgian, Swiss and French francs; the Canadian dollar; the German mark; the Danish and Norwegian kroners; the British and Irish pounds; the Italian lira; the Japanese yen and the Dutch guilder. The CHMs captured in a satisfactory way the volatility clustering of the series and show volatility peaks in historically nervous periods of the international market. Moreover, the results of the BDS tests for whiteness applied to the standardized residuals show the good specification of the models. Copyright © 1998 John Wiley & Sons, Ltd. 相似文献
40.
Sotoodehnia N Isaacs A de Bakker PI Dörr M Newton-Cheh C Nolte IM van der Harst P Müller M Eijgelsheim M Alonso A Hicks AA Padmanabhan S Hayward C Smith AV Polasek O Giovannone S Fu J Magnani JW Marciante KD Pfeufer A Gharib SA Teumer A Li M Bis JC Rivadeneira F Aspelund T Köttgen A Johnson T Rice K Sie MP Wang YA Klopp N Fuchsberger C Wild SH Mateo Leach I Estrada K Völker U Wright AF Asselbergs FW Qu J Chakravarti A Sinner MF Kors JA Petersmann A Harris TB Soliman EZ Munroe PB Psaty BM 《Nature genetics》2010,42(12):1068-1076