17 research outputs found

    Spatial trends of dry spells over Peninsular Malaysia during monsoon seasons

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    This study aims to trace changes in the dry spells over Peninsular Malaysia based on the daily rainfall data from 36 selected rainfall stations which include four subregions, namely northwest, west, southwest, and east for the periods of 1975 to 2004. Six dry spell indices comprising of the main characteristics of dry spells, the persistency of dry events, and the frequency of the short and long duration of dry spells will be used to identify whether or not these indices have increased or decreased over Peninsular Malaysia during the monsoon seasons. The findings of this study indicate that the northwestern areas of the Peninsular could be considered as the driest area since almost all the indices of dry spells over these areas are higher than in the other regions during the northeast (NE) monsoon. Based on the individual and the field significant trends, the results of the Mann–Kendall test indicate that as the total number of dry days, the maximum duration, the mean, and the persistency of dry days are decreased, the trend of the frequency of long dry spells of at least 4 days is also found to decrease in almost all the stations over the Peninsula; however, an increasing trend is observed in the frequency of short spells in these stations during the NE monsoon season. On the other hand, during the southwest monsoon, a positive trend is observed in the characteristics of dry spells including the persistency of two dry days in many stations over the Peninsula. The frequency of longer dry periods exhibits a decreasing trend in most stations over the western areas during both monsoon seasons for the periods of 1975 to 2004

    Evaluating the accuracy of genomic prediction of growth and wood traits in two Eucalyptus species and their F-1 hybrids

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    Background: Genomic prediction is a genomics assisted breeding methodology that can increase genetic gains by accelerating the breeding cycle and potentially improving the accuracy of breeding values. In this study, we use 41,304 informative SNPs genotyped in a Eucalyptus breeding population involving 90 E. grandis and 78 E. urophylla parents and their 949 F-1 hybrids to develop genomic prediction models for eight phenotypic traits-basic density and pulp yield, circumference at breast height and height and tree volume scored at age three and six years. We assessed the impact of different genomic prediction methods, the composition and size of the training and validation set and the number and genomic location of SNPs on the predictive ability (PA). Results: Heritabilities estimated using the realized genomic relationship matrix (GRM) were considerably higher than estimates based on the expected pedigree, mainly due to inconsistencies in the expected pedigree that were readily corrected by the GRM. Moreover, the GRM more precisely capture Mendelian sampling among related individuals, such that the genetic covariance was based on the true proportion of the genome shared between individuals. PA improved considerably when increasing the size of the training set and by enhancing relatedness to the validation set. Prediction models trained on pure species parents could not predict well in F-1 hybrids, indicating that model training has to be carried out in hybrid populations if one is to predict in hybrid selection candidates. The different genomic prediction methods provided similar results for all traits, therefore either GBLUP or rrBLUP represents better compromises between computational time and prediction efficiency. Only slight improvement was observed in PA when more than 5000 SNPs were used for all traits. Using SNPs in intergenic regions provided slightly better PA than using SNPs sampled exclusively in genic regions. Conclusions: The size and composition of the training set and number of SNPs used are the two most important factors for model prediction, compared to the statistical methods and the genomic location of SNPs. Furthermore, training the prediction model based on pure parental species only provide limited ability to predict traits in interspecific hybrids. Our results provide additional promising perspectives for the implementation of genomic prediction in Eucalyptus breeding programs by the selection of interspecific hybrids

    Internalization and desensitization of adenosine receptors.

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    Contains fulltext : 69662.pdf (publisher's version ) (Closed access)Until now, more than 800 distinct G protein-coupled receptors (GPCRs) have been identified in the human genome. The four subtypes of the adenosine receptor (A(1), A(2A), A(2B) and A(3) receptor) belong to this large family of GPCRs that represent the most widely targeted pharmacological protein class. Since adenosine receptors are widespread throughout the body and involved in a variety of physiological processes and diseases, there is great interest in understanding how the different subtypes are regulated, as a basis for designing therapeutic drugs that either avoid or make use of this regulation. The major GPCR regulatory pathway involves phosphorylation of activated receptors by G protein-coupled receptor kinases (GRKs), a process that is followed by binding of arrestin proteins. This prevents receptors from activating downstream heterotrimeric G protein pathways, but at the same time allows activation of arrestin-dependent signalling pathways. Upon agonist treatment, adenosine receptor subtypes are differently regulated. For instance, the A(1)Rs are not (readily) phosphorylated and internalize slowly, showing a typical half-life of several hours, whereas the A(2A)R and A(2B)R undergo much faster downregulation, usually shorter than 1 h. The A(3)R is subject to even faster downregulation, often a matter of minutes. The fast desensitization of the A(3)R after agonist exposure may be therapeutically equivalent to antagonist occupancy of the receptor. This review describes the process of desensitization and internalization of the different adenosine subtypes in cell systems, tissues and in vivo studies. In addition, molecular mechanisms involved in adenosine receptor desensitization are discussed
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