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通过整合来自文献、数据库和计算工具的信息来做出基础科学发现——一个例子。

Making fundamental scientific discoveries by combining information from literature, databases, and computational tools - An example.

作者信息

Stielow Bastian, Simon Clara, Liefke Robert

机构信息

Institute of Molecular Biology and Tumor Research (IMT), Philipps University of Marburg, 35043 Marburg, Germany.

Department of Hematology, Oncology and Immunology, University Hospital Giessen and Marburg, 35043 Marburg, Germany.

出版信息

Comput Struct Biotechnol J. 2021 May 14;19:3027-3033. doi: 10.1016/j.csbj.2021.04.052. eCollection 2021.

DOI:10.1016/j.csbj.2021.04.052
PMID:34136100
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8175269/
Abstract

In recent years, the amount of available literature, data and computational tools has increased exponentially, providing opportunities and challenges to make use of this vast amount of material. Here, we describe how we utilized publicly available information to identify the previously hardly characterized protein SAMD1 (SAM domain-containing protein 1) as a novel unmethylated CpG island-binding protein. This discovery is an example, how the richness of material and tools on the internet can be used to make scientific breakthroughs, but also the hurdles that may occur. Specifically, we discuss how the misrepresentation of SAMD1 in literature and databases may have prevented an earlier characterization of this protein and we address what can be learned from this example.

摘要

近年来,可用文献、数据和计算工具的数量呈指数级增长,这为利用这些海量资料带来了机遇与挑战。在此,我们描述了我们如何利用公开可用信息,将此前几乎未被表征的含SAM结构域蛋白1(SAMD1)鉴定为一种新型的未甲基化CpG岛结合蛋白。这一发现例证了互联网上丰富的资料和工具如何能够用于实现科学突破,同时也展示了可能出现的障碍。具体而言,我们讨论了文献和数据库中SAMD1的错误表述可能如何阻碍了对该蛋白的早期表征,并探讨了能从这个例子中学到什么。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1864/8175269/9fd6f7a6c581/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1864/8175269/edb04c1c5be2/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1864/8175269/1f588a15d0c5/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1864/8175269/d4b327a28fcf/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1864/8175269/9fd6f7a6c581/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1864/8175269/edb04c1c5be2/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1864/8175269/1f588a15d0c5/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1864/8175269/d4b327a28fcf/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1864/8175269/9fd6f7a6c581/gr4.jpg

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本文引用的文献

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The SAM domain-containing protein 1 (SAMD1) acts as a repressive chromatin regulator at unmethylated CpG islands.SAM 结构域蛋白 1(SAMD1)作为未甲基化 CpG 岛的抑制性染色质调节剂发挥作用。
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SMART: recent updates, new developments and status in 2020.SMART:最新更新、新进展和 2020 年的现状。
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Visualizing and interpreting cancer genomics data via the Xena platform.通过Xena平台可视化和解读癌症基因组学数据。
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Investigation of SAMD1 ablation in mice.研究 SAMD1 基因敲除小鼠。
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The histone acetyltransferase KAT6A is recruited to unmethylated CpG islands via a DNA binding winged helix domain.组蛋白乙酰转移酶 KAT6A 通过一个 DNA 结合的翼状螺旋结构域被招募到未甲基化的 CpG 岛上。
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The CpG Island-Binding Protein SAMD1 Contributes to an Unfavorable Gene Signature in HepG2 Hepatocellular Carcinoma Cells.CpG岛结合蛋白SAMD1促成HepG2肝癌细胞中不良基因特征的形成。
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