4.8 Article

Ribo-uORF: a comprehensive data resource of upstream open reading frames (uORFs) based on ribosome profiling

期刊

NUCLEIC ACIDS RESEARCH
卷 51, 期 D1, 页码 D248-D261

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkac1094

关键词

-

向作者/读者索取更多资源

The study developed two tools, Ribo-uORF and mRNAbrowse, for studying the function and gene expression regulation of uORFs, providing a comprehensive uORF data resource and an easy-to-use web interface. Additionally, uORFscan and UTR5var were developed for accurate identification of uORFs and analysis of the effects of genetic mutations.
Upstream open reading frames (uORFs) are typically defined as translation sites located within the 5 & PRIME; untranslated region upstream of the main protein coding sequence (CDS) of messenger RNAs (mRNAs). Although uORFs are prevalent in eukaryotic mRNAs and modulate the translation of downstream CDSs, a comprehensive resource for uORFs is currently lacking. We developed Ribo-uORF () to serve as a comprehensive functional resource for uORF analysis based on ribosome profiling (Ribo-seq) data. Ribo-uORF currently supports six species: human, mouse, rat, zebrafish, fruit fly, and worm. Ribo-uORF includes 501 554 actively translated uORFs and 107 914 upstream translation initiation sites (uTIS), which were identified from 1495 Ribo-seq and 77 quantitative translation initiation sequencing (QTI-seq) datasets, respectively. We also developed mRNAbrowse to visualize items such as uORFs, cis-regulatory elements, genetic variations, eQTLs, GWAS-based associations, RNA modifications, and RNA editing. Ribo-uORF provides a very intuitive web interface for conveniently browsing, searching, and visualizing uORF data. Finally, uORFscan and UTR5var were developed in Ribo-uORF to precisely identify uORFs and analyze the influence of genetic mutations on uORFs using user-uploaded datasets. Ribo-uORF should greatly facilitate studies of uORFs and their roles in mRNA translation and posttranscriptional control of gene expression.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据