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Figure 1. (A) Overview of ENPD including data source, data processing and features. Transcriptomes from TSA, genomes ... Figure 1. (A) Overview of ENPD.

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Presentation on theme: "Figure 1. (A) Overview of ENPD including data source, data processing and features. Transcriptomes from TSA, genomes ... Figure 1. (A) Overview of ENPD."— Presentation transcript:

1 Figure 1. (A) Overview of ENPD including data source, data processing and features. Transcriptomes from TSA, genomes ... Figure 1. (A) Overview of ENPD including data source, data processing and features. Transcriptomes from TSA, genomes from NCBI and primary literature were used as data sources for the construction of eukaryotic nucleic acid binding protein database (ENPD). Recording the 3 types of NBPs in eukaryotes: DBPs, RBPs and DRBPs. The basic information of NBPs as well as their functional and regulatory information are also curated by both prediction and manual. See text for details. Unless provided in the caption above, the following copyright applies to the content of this slide: © The Author(s) Published by Oxford University Press on behalf of Nucleic Acids Research.This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact Nucleic Acids Research, Volume 47, Issue D1, 24 November 2018, Pages D322–D329, The content of this slide may be subject to copyright: please see the slide notes for details.

2 Figure 2. Functions of TFs, RBPs and DRBPs in ENPD
Figure 2. Functions of TFs, RBPs and DRBPs in ENPD. NBPs are involved in every stage of gene regulation and are ... Figure 2. Functions of TFs, RBPs and DRBPs in ENPD. NBPs are involved in every stage of gene regulation and are important in most if not all biological processes through interactions with DNAs and RNAs, controlling cell identity and pathological status. (A) TFs usually bind to DNA regulatory elements of a gene and regulate its transcription activity, while (B) RBPs have diverse functions related to mRNA regulation, including alternative splicing, mRNA stability control, and degradation. (C) The two types of proteins can cooperate to recruit ncRNA for subsequent transcriptional activator recruitment. DRBPs have a wide range of distinct functions: (D) functioning as a typical TF with add-on abilities such as interacting with ncRNA decoys; (E) recruiting ncRNA with co-activator function; (F) regulating mRNAs and DNA regulatory elements just as typical RBPs and TFs, with the two functions competing for the same protein; (G) interacting with lncRNA for stability enhancement, thus increasing DRBP abundance and further activating downstream gene transcriptions and (H) altering the phosphorylation status by the mediation of lncRNA, enhancing the gene activating activity. Unless provided in the caption above, the following copyright applies to the content of this slide: © The Author(s) Published by Oxford University Press on behalf of Nucleic Acids Research.This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact Nucleic Acids Research, Volume 47, Issue D1, 24 November 2018, Pages D322–D329, The content of this slide may be subject to copyright: please see the slide notes for details.

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