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  • 1
    Publication Date: 2016-03-01
    Description: RNA-binding proteins (RBPs) play important roles in the post-transcriptional control of RNAs. Identifying RBP binding sites and characterizing RBP binding preferences are key steps toward understanding the basic mechanisms of the post-transcriptional gene regulation. Though numerous computational methods have been developed for modeling RBP binding preferences, discovering a complete structural representation of the RBP targets by integrating their available structural features in all three dimensions is still a challenging task. In this paper, we develop a general and flexible deep learning framework for modeling structural binding preferences and predicting binding sites of RBPs, which takes (predicted) RNA tertiary structural information into account for the first time . Our framework constructs a unified representation that characterizes the structural specificities of RBP targets in all three dimensions, which can be further used to predict novel candidate binding sites and discover potential binding motifs. Through testing on the real CLIP-seq datasets, we have demonstrated that our deep learning framework can automatically extract effective hidden structural features from the encoded raw sequence and structural profiles, and predict accurate RBP binding sites. In addition, we have conducted the first study to show that integrating the additional RNA tertiary structural features can improve the model performance in predicting RBP binding sites, especially for the polypyrimidine tract-binding protein (PTB), which also provides a new evidence to support the view that RBPs may own specific tertiary structural binding preferences. In particular, the tests on the internal ribosome entry site (IRES) segments yield satisfiable results with experimental support from the literature and further demonstrate the necessity of incorporating RNA tertiary structural information into the prediction model. The source code of our approach can be found in https://github.com/thucombio/deepnet-rbp .
    Keywords: Nucleic acid structure, Protein-nucleic acid interaction, Computational Methods
    Print ISSN: 0305-1048
    Electronic ISSN: 1362-4962
    Topics: Biology
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  • 2
    Publication Date: 2015-06-10
    Description: Modified Newtonian dynamics (MOND) proposed by Milgrom provides a paradigm alternative to dark matter (DM) that has been successful in fitting and predicting the rich phenomenology of rotating disc galaxies. There have also been attempts to test MOND in dispersion-supported spheroidal early-type galaxies, but it remains unclear whether MOND can fit the various empirical properties of early-type galaxies for the whole ranges of mass and radius. As a way of rigorously testing MOND in elliptical galaxies we calculate the MOND-predicted velocity dispersion profiles (VDPs) in the inner regions of ~2000 nearly round Sloan Digital Sky Survey elliptical galaxies under a variety of assumptions on velocity dispersion (VD) anisotropy, and then compare the predicted distribution of VDP slopes with the observed distribution in 11 ATLAS 3D galaxies selected with essentially the same criteria. We find that the MOND model parametrized with an interpolating function that works well for rotating galaxies can also reproduce the observed distribution of VDP slopes based only on the observed stellar mass distribution without DM or any other galaxy-to-galaxy varying factor. This is remarkable in view that Newtonian dynamics with DM requires a specific amount and/or profile of DM for each galaxy in order to reproduce the observed distribution of VDP slopes. When we analyse non-round galaxy samples using the MOND-based spherical Jeans equation, we do not find any systematic difference in the mean property of the VDP slope distribution compared with the nearly round sample. However, in line with previous studies of MOND through individual analyses of elliptical galaxies, varying MOND interpolating function or VD anisotropy can lead to systematic change in the VDP slope distribution, indicating that a statistical analysis of VDPs can be used to constrain specific MOND models with an accurate measurement of VDP slopes or a prior constraint on VD anisotropy.
    Print ISSN: 0035-8711
    Electronic ISSN: 1365-2966
    Topics: Physics
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  • 3
    Publication Date: 2015-06-12
    Description: Modified Newtonian dynamics (MOND) proposed by Milgrom provides a paradigm alternative to dark matter (DM) that has been successful in fitting and predicting the rich phenomenology of rotating disc galaxies. There have also been attempts to test MOND in dispersion-supported spheroidal early-type galaxies, but it remains unclear whether MOND can fit the various empirical properties of early-type galaxies for the whole ranges of mass and radius. As a way of rigorously testing MOND in elliptical galaxies we calculate the MOND-predicted velocity dispersion profiles (VDPs) in the inner regions of ~2000 nearly round Sloan Digital Sky Survey elliptical galaxies under a variety of assumptions on velocity dispersion (VD) anisotropy, and then compare the predicted distribution of VDP slopes with the observed distribution in 11 ATLAS 3D galaxies selected with essentially the same criteria. We find that the MOND model parametrized with an interpolating function that works well for rotating galaxies can also reproduce the observed distribution of VDP slopes based only on the observed stellar mass distribution without DM or any other galaxy-to-galaxy varying factor. This is remarkable in view that Newtonian dynamics with DM requires a specific amount and/or profile of DM for each galaxy in order to reproduce the observed distribution of VDP slopes. When we analyse non-round galaxy samples using the MOND-based spherical Jeans equation, we do not find any systematic difference in the mean property of the VDP slope distribution compared with the nearly round sample. However, in line with previous studies of MOND through individual analyses of elliptical galaxies, varying MOND interpolating function or VD anisotropy can lead to systematic change in the VDP slope distribution, indicating that a statistical analysis of VDPs can be used to constrain specific MOND models with an accurate measurement of VDP slopes or a prior constraint on VD anisotropy.
    Print ISSN: 0035-8711
    Electronic ISSN: 1365-2966
    Topics: Physics
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  • 4
    Publication Date: 2014-04-15
    Description: ALKBH5 is a 2-oxoglutarate (2OG) and ferrous iron-dependent nucleic acid oxygenase (NAOX) that catalyzes the demethylation of N 6 -methyladenine in RNA. ALKBH5 is upregulated under hypoxia and plays a role in spermatogenesis. We describe a crystal structure of human ALKBH5 (residues 66–292) to 2.0 Å resolution. ALKBH5 66–292 has a double-stranded β-helix core fold as observed in other 2OG and iron-dependent oxygenase family members. The active site metal is octahedrally coordinated by an HXD...H motif (comprising residues His204, Asp206 and His266) and three water molecules. ALKBH5 shares a nucleotide recognition lid and conserved active site residues with other NAOXs. A large loop (βIV–V) in ALKBH5 occupies a similar region as the L1 loop of the fat mass and obesity-associated protein that is proposed to confer single-stranded RNA selectivity. Unexpectedly, a small molecule inhibitor, IOX3, was observed covalently attached to the side chain of Cys200 located outside of the active site. Modelling substrate into the active site based on other NAOX–nucleic acid complexes reveals conserved residues important for recognition and demethylation mechanisms. The structural insights will aid in the development of inhibitors selective for NAOXs, for use as functional probes and for therapeutic benefit.
    Print ISSN: 0305-1048
    Electronic ISSN: 1362-4962
    Topics: Biology
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  • 5
    Publication Date: 2016-04-21
    Description: Genome-wide proximity ligation assays allow the identification of chromatin contacts at unprecedented resolution. Several studies reveal that mammalian chromosomes are composed of topological domains (TDs) in sub-mega base resolution, which appear to be conserved across cell types and to some extent even between organisms. Identifying topological domains is now an important step toward understanding the structure and functions of spatial genome organization. However, current methods for TD identification demand extensive computational resources, require careful tuning and/or encounter inconsistencies in results. In this work, we propose an efficient and deterministic method, TopDom, to identify TDs, along with a set of statistical methods for evaluating their quality. TopDom is much more efficient than existing methods and depends on just one intuitive parameter, a window size, for which we provide easy-to-implement optimization guidelines. TopDom also identifies more and higher quality TDs than the popular directional index algorithm. The TDs identified by TopDom provide strong support for the cross-tissue TD conservation. Finally, our analysis reveals that the locations of housekeeping genes are closely associated with cross-tissue conserved TDs. The software package and source codes of TopDom are available at http://zhoulab.usc.edu/TopDom/ .
    Print ISSN: 0305-1048
    Electronic ISSN: 1362-4962
    Topics: Biology
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  • 6
    Publication Date: 2012-11-25
    Description: Translational GTPases (trGTPases) regulate all phases of protein synthesis. An early event in the interaction of a trGTPase with the ribosome is the contact of the G-domain with the C-terminal domain (CTD) of ribosomal protein L12 (L12-CTD) and subsequently interacts with the N-terminal domain of L11 (L11-NTD). However, the structural and functional relationships between L12-CTD and L11-NTD remain unclear. Here, we performed mutagenesis, biochemical and structural studies to identify the interactions between L11-NTD and L12-CTD. Mutagenesis of conserved residues in the interaction site revealed their role in the docking of trGTPases. During docking, loop62 of L11-NTD protrudes into a cleft in L12-CTD, leading to an open conformation of this domain and exposure of hydrophobic core. This unfavorable situation for L12-CTD stability is resolved by a chaperone-like activity of the contacting G-domain. Our results suggest that all trGTPases—regardless of their different specific functions—use a common mechanism for stabilizing the L11-NTD•L12-CTD interactions.
    Print ISSN: 0305-1048
    Electronic ISSN: 1362-4962
    Topics: Biology
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  • 7
    Publication Date: 2014-09-24
    Description: Protein phosphorylation is one of the most pervasive post-translational modifications, regulating diverse cellular processes in various organisms. As mass spectrometry-based experimental approaches for identifying phosphorylation events are resource-intensive, many computational methods have been proposed, in which phosphorylation site prediction is formulated as a classification problem. They differ in several ways, and one crucial issue is the construction of training data and test data for unbiased performance evaluation. In this article, we categorize the existing data construction methods and try to answer three questions: (i) Is it equivalent to use different data construction methods in the assessment of phosphorylation site prediction algorithms? (ii) What kind of test data set is unbiased for assessing the prediction performance of a trained algorithm in different real world scenarios? (iii) Among the summarized training data construction methods, which one(s) has better generalization performance for most scenarios? To answer these questions, we conduct comprehensive experimental studies for both non-kinase-specific and kinase-specific prediction tasks. The experimental results show that: (i) different data construction methods can lead to significantly different prediction performance; (ii) there can be different test data construction methods that are unbiased with respect to different real world scenarios; and (iii) different data construction methods have different generalization performance in different real world scenarios. Therefore, when developing new algorithms in future research, people should concentrate on what kind of scenario their algorithm will work for, what the corresponding unbiased test data are and which training data construction method can generate best generalization performance.
    Print ISSN: 1467-5463
    Electronic ISSN: 1477-4054
    Topics: Biology , Computer Science
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  • 8
    Publication Date: 2015-01-07
    Description: More than 30 amyloid proteins are reported to be associated with amyloidosis diseases. Studies have implicated histidine may be critically involved in amyloid formation. Here, we used diethylpyrocarbonate (DEPC) modification to obtain a His B5 mono-ethyloxyformylated insulin (DMI-B 5 ). The secondary structure, amyloidogenicity, metal ion interaction, and cytotoxicity of DMI-B 5 and insulin were compared. DMI-B 5 was less prone to aggregation in acidic condition but easier to aggregate at neutral pH. DEPC modification resulted in attenuated inhibitory effect of Zn 2+ on aggregation, whereas DMI-B 5 fibrils induced more severe erythrocytes haemolysis compared to insulin fibrils. This study not only provides a fast new approach for studying the impact of imidazole ring in amyloid formation, but also reveals the critical modulating role of histidine imidazole ring on the amyloidogenicity of insulin.
    Print ISSN: 0021-924X
    Electronic ISSN: 1756-2651
    Topics: Biology , Chemistry and Pharmacology
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  • 9
    Publication Date: 2012-08-08
    Description: Contact: zyhe@dlut.edu.cn
    Print ISSN: 1367-4803
    Electronic ISSN: 1460-2059
    Topics: Biology , Computer Science , Medicine
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  • 10
    Publication Date: 2017-01-05
    Description: The Chemical Effects in Biological Systems database (CEBS) is a comprehensive and unique toxicology resource that compiles individual and summary animal data from the National Toxicology Program (NTP) testing program and other depositors into a single electronic repository. CEBS has undergone significant updates in recent years and currently contains over 11 000 test articles (exposure agents) and over 8000 studies including all available NTP carcinogenicity, short-term toxicity and genetic toxicity studies. Study data provided to CEBS are manually curated, accessioned and subject to quality assurance review prior to release to ensure high quality. The CEBS database has two main components: data collection and data delivery. To accommodate the breadth of data produced by NTP, the CEBS data collection component is an integrated relational design that allows the flexibility to capture any type of electronic data (to date). The data delivery component of the database comprises a series of dedicated user interface tables containing pre-processed data that support each component of the user interface. The user interface has been updated to include a series of nine Guided Search tools that allow access to NTP summary and conclusion data and larger non-NTP datasets. The CEBS database can be accessed online at http://www.niehs.nih.gov/research/resources/databases/cebs/ .
    Print ISSN: 0305-1048
    Electronic ISSN: 1362-4962
    Topics: Biology
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