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miRdSNP:一个疾病相关 SNP 数据库和人类基因 3'UTR 上 microRNA 靶位。

miRdSNP: a database of disease-associated SNPs and microRNA target sites on 3'UTRs of human genes.

机构信息

Center for Computational Research, New York State Center of Excellence in Bioinformatics & Life Sciences, State University of New York at Buffalo, Buffalo, NY 14260, USA.

出版信息

BMC Genomics. 2012 Jan 25;13:44. doi: 10.1186/1471-2164-13-44.

Abstract

BACKGROUND

Single nucleotide polymorphisms (SNPs) can lead to the susceptibility and onset of diseases through their effects on gene expression at the posttranscriptional level. Recent findings indicate that SNPs could create, destroy, or modify the efficiency of miRNA binding to the 3'UTR of a gene, resulting in gene dysregulation. With the rapidly growing number of published disease-associated SNPs (dSNPs), there is a strong need for resources specifically recording dSNPs on the 3'UTRs and their nucleotide distance from miRNA target sites. We present here miRdSNP, a database incorporating three important areas of dSNPs, miRNA target sites, and diseases.

DESCRIPTION

miRdSNP provides a unique database of dSNPs on the 3'UTRs of human genes manually curated from PubMed. The current release includes 786 dSNP-disease associations for 630 unique dSNPs and 204 disease types. miRdSNP annotates genes with experimentally confirmed targeting by miRNAs and indexes miRNA target sites predicted by TargetScan and PicTar as well as potential miRNA target sites newly generated by dSNPs. A robust web interface and search tools are provided for studying the proximity of miRNA binding sites to dSNPs in relation to human diseases. Searches can be dynamically filtered by gene name, miRBase ID, target prediction algorithm, disease, and any nucleotide distance between dSNPs and miRNA target sites. Results can be viewed at the sequence level showing the annotated locations for miRNA target sites and dSNPs on the entire 3'UTR sequences. The integration of dSNPs with the UCSC Genome browser is also supported.

CONCLUSION

miRdSNP provides a comprehensive data source of dSNPs and robust tools for exploring their distance from miRNA target sites on the 3'UTRs of human genes. miRdSNP enables researchers to further explore the molecular mechanism of gene dysregulation for dSNPs at posttranscriptional level. miRdSNP is freely available on the web at http://mirdsnp.ccr.buffalo.edu.

摘要

背景

单核苷酸多态性 (SNP) 可通过影响基因在转录后水平的表达而导致疾病的易感性和发病。最近的研究结果表明,SNP 可能会产生、破坏或改变 miRNA 与基因 3'UTR 结合的效率,从而导致基因失调。随着已发表的与疾病相关的 SNP(dSNP)数量的迅速增加,人们强烈需要专门记录 3'UTR 上的 dSNP 及其与 miRNA 靶位点的核苷酸距离的资源。我们在此介绍 miRdSNP,这是一个整合了 dSNP、miRNA 靶位点和疾病三个重要领域的数据库。

描述

miRdSNP 提供了一个手动从 PubMed 中整理的人类基因 3'UTR 上的 dSNP 的独特数据库。当前版本包括 630 个独特的 dSNP 中的 786 个 dSNP-疾病关联和 204 种疾病类型。miRdSNP 对具有 miRNA 实验证实靶向作用的基因进行注释,并对 TargetScan 和 PicTar 预测的 miRNA 靶位点以及由 dSNP 新产生的潜在 miRNA 靶位点进行索引。提供了一个强大的 Web 界面和搜索工具,用于研究 miRNA 结合位点与人类疾病相关的 dSNP 的接近程度。搜索可以通过基因名称、miRBase ID、靶标预测算法、疾病以及 dSNP 和 miRNA 靶位点之间的任何核苷酸距离动态筛选。结果可以在序列级别查看,显示 miRNA 靶位点和 3'UTR 上的整个 dSNP 序列的注释位置。还支持 dSNP 与 UCSC 基因组浏览器的集成。

结论

miRdSNP 提供了一个全面的 dSNP 数据源和强大的工具,用于探索它们在人类基因 3'UTR 上与 miRNA 靶位点的距离。miRdSNP 使研究人员能够进一步探索 dSNP 在转录后水平导致基因失调的分子机制。miRdSNP 可在 http://mirdsnp.ccr.buffalo.edu 上免费获取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3c0/3287127/a1cfba5a11b2/1471-2164-13-44-1.jpg

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