• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

APPRIS 2017:多个基因集的主要同工型。

APPRIS 2017: principal isoforms for multiple gene sets.

机构信息

Spanish National Bioinformatics Institute (INB), Spanish National Cancer Research Centre (CNIO), Madrid 28029, Spain.

Structural Biology and Biocomputing Programme, Spanish National Cancer Research Centre (CNIO), Madrid 28029, Spain.

出版信息

Nucleic Acids Res. 2018 Jan 4;46(D1):D213-D217. doi: 10.1093/nar/gkx997.

DOI:10.1093/nar/gkx997
PMID:29069475
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5753224/
Abstract

The APPRIS database (http://appris-tools.org) uses protein structural and functional features and information from cross-species conservation to annotate splice isoforms in protein-coding genes. APPRIS selects a single protein isoform, the 'principal' isoform, as the reference for each gene based on these annotations. A single main splice isoform reflects the biological reality for most protein coding genes and APPRIS principal isoforms are the best predictors of these main proteins isoforms. Here, we present the updates to the database, new developments that include the addition of three new species (chimpanzee, Drosophila melangaster and Caenorhabditis elegans), the expansion of APPRIS to cover the RefSeq gene set and the UniProtKB proteome for six species and refinements in the core methods that make up the annotation pipeline. In addition APPRIS now provides a measure of reliability for individual principal isoforms and updates with each release of the GENCODE/Ensembl and RefSeq reference sets. The individual GENCODE/Ensembl, RefSeq and UniProtKB reference gene sets for six organisms have been merged to produce common sets of splice variants.

摘要

APPRIS 数据库(http://appris-tools.org)使用蛋白质结构和功能特征以及跨物种保守信息来注释蛋白质编码基因中的剪接异构体。APPRIS 根据这些注释,选择单个蛋白质异构体,即“主要”异构体,作为每个基因的参考。大多数蛋白质编码基因的单个主要剪接异构体反映了生物学现实,而 APPRIS 主要异构体是这些主要蛋白质异构体的最佳预测因子。在这里,我们介绍了数据库的更新,包括三个新物种(黑猩猩、果蝇和秀丽隐杆线虫)的添加,APPRIS 扩展到涵盖 RefSeq 基因集和六个物种的 UniProtKB 蛋白质组,以及构成注释管道的核心方法的改进。此外,APPRIS 现在为每个主要异构体提供了可靠性度量,并在 GENCODE/Ensembl 和 RefSeq 参考集的每次更新中进行更新。已经合并了六个生物体的单个 GENCODE/Ensembl、RefSeq 和 UniProtKB 参考基因集,以生成常见的剪接变体集。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fef/5753224/dcc9ca1929d0/gkx997fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fef/5753224/6f31f77010fb/gkx997fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fef/5753224/dcc9ca1929d0/gkx997fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fef/5753224/6f31f77010fb/gkx997fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fef/5753224/dcc9ca1929d0/gkx997fig2.jpg

相似文献

1
APPRIS 2017: principal isoforms for multiple gene sets.APPRIS 2017:多个基因集的主要同工型。
Nucleic Acids Res. 2018 Jan 4;46(D1):D213-D217. doi: 10.1093/nar/gkx997.
2
APPRIS: annotation of principal and alternative splice isoforms.APPRIS:主要和替代剪接异构体的注释。
Nucleic Acids Res. 2013 Jan;41(Database issue):D110-7. doi: 10.1093/nar/gks1058. Epub 2012 Nov 17.
3
APPRIS WebServer and WebServices.APPRIS网络服务器和网络服务。
Nucleic Acids Res. 2015 Jul 1;43(W1):W455-9. doi: 10.1093/nar/gkv512. Epub 2015 May 18.
4
APPRIS principal isoforms and MANE Select transcripts define reference splice variants.APPRIS 主要异构体和 MANE Select 转录本定义参考剪接变体。
Bioinformatics. 2022 Sep 16;38(Suppl_2):ii89-ii94. doi: 10.1093/bioinformatics/btac473.
5
APPRIS: selecting functionally important isoforms.APPRIS:选择具有重要功能的异构体。
Nucleic Acids Res. 2022 Jan 7;50(D1):D54-D59. doi: 10.1093/nar/gkab1058.
6
Comparison of GENCODE and RefSeq gene annotation and the impact of reference geneset on variant effect prediction.GENCODE与RefSeq基因注释的比较以及参考基因集对变异效应预测的影响。
BMC Genomics. 2015;16 Suppl 8(Suppl 8):S2. doi: 10.1186/1471-2164-16-S8-S2. Epub 2015 Jun 18.
7
ISOGO: Functional annotation of protein-coding splice variants.ISOGO:蛋白质编码剪接变体的功能注释。
Sci Rep. 2020 Jan 23;10(1):1069. doi: 10.1038/s41598-020-57974-z.
8
Functional Networks of Highest-Connected Splice Isoforms: From The Chromosome 17 Human Proteome Project.高连接性剪接异构体的功能网络:来自17号染色体人类蛋白质组计划
J Proteome Res. 2015 Sep 4;14(9):3484-91. doi: 10.1021/acs.jproteome.5b00494. Epub 2015 Aug 11.
9
Comparison of RefSeq protein-coding regions in human and vertebrate genomes.比较人类和脊椎动物基因组中的 RefSeq 编码蛋白区域。
BMC Genomics. 2013 Sep 25;14:654. doi: 10.1186/1471-2164-14-654.
10
Alternatively Spliced Homologous Exons Have Ancient Origins and Are Highly Expressed at the Protein Level.选择性剪接的同源外显子具有古老的起源,并且在蛋白质水平上高度表达。
PLoS Comput Biol. 2015 Jun 10;11(6):e1004325. doi: 10.1371/journal.pcbi.1004325. eCollection 2015 Jun.

引用本文的文献

1
A spatial long-read approach at near-single-cell resolution reveals developmental regulation of splicing and polyadenylation sites in distinct cortical layers and cell types.一种接近单细胞分辨率的空间长读长方法揭示了不同皮质层和细胞类型中剪接和聚腺苷酸化位点的发育调控。
Nat Commun. 2025 Aug 29;16(1):8093. doi: 10.1038/s41467-025-63301-9.
2
Transcriptome-wide decoding the roles of aberrant splicing in melanoma MAPK-targeted resistance evolution.全转录组范围解码异常剪接在黑色素瘤MAPK靶向耐药进化中的作用。
EMBO Rep. 2025 Jul 18. doi: 10.1038/s44319-025-00521-6.
3
A spatial long-read approach at near-single-cell resolution reveals developmental regulation of splicing and polyadenylation sites in distinct cortical layers and cell types.

本文引用的文献

1
Most Alternative Isoforms Are Not Functionally Important.大多数可变异构体在功能上并不重要。
Trends Biochem Sci. 2017 Jun;42(6):408-410. doi: 10.1016/j.tibs.2017.04.002. Epub 2017 May 5.
2
The Relationship between Alternative Splicing and Proteomic Complexity.可变剪接与蛋白质组复杂性之间的关系。
Trends Biochem Sci. 2017 Jun;42(6):407-408. doi: 10.1016/j.tibs.2017.04.001. Epub 2017 May 5.
3
The UCSC Genome Browser database: 2017 update.加州大学圣克鲁兹分校基因组浏览器数据库:2017年更新版
一种接近单细胞分辨率的空间长读长方法揭示了不同皮质层和细胞类型中剪接和聚腺苷酸化位点的发育调控。
bioRxiv. 2025 Jun 10:2025.06.10.658877. doi: 10.1101/2025.06.10.658877.
4
Spatial transcriptomics in the adult brain and body.成人大脑和身体中的空间转录组学。
Elife. 2025 Mar 18;13:RP92618. doi: 10.7554/eLife.92618.
5
Notable challenges posed by long-read sequencing for the study of transcriptional diversity and genome annotation.长读长测序在转录多样性研究和基因组注释方面带来的显著挑战。
Genome Res. 2025 Apr 14;35(4):583-592. doi: 10.1101/gr.279865.124.
6
An organotypic atlas of human vascular cells.人类血管细胞的器官型图谱。
Nat Med. 2024 Dec;30(12):3468-3481. doi: 10.1038/s41591-024-03376-x. Epub 2024 Nov 20.
7
Re-appraising the evidence for the source, regulation and function of p53-family isoforms.重新评估 p53 家族同工型的来源、调控和功能的证据。
Nucleic Acids Res. 2024 Nov 11;52(20):12112-12129. doi: 10.1093/nar/gkae855.
8
Participation of ventricular trabeculae in neonatal cardiac regeneration leads to ectopic recruitment of Purkinje-like cells.室嵴参与新生儿心脏再生导致浦肯野样细胞的异位募集。
Nat Cardiovasc Res. 2024 Sep;3(9):1140-1157. doi: 10.1038/s44161-024-00530-z. Epub 2024 Aug 28.
9
Single-cell long-read sequencing-based mapping reveals specialized splicing patterns in developing and adult mouse and human brain.基于单细胞长读测序的映射揭示了发育中和成年鼠和人脑的特异性剪接模式。
Nat Neurosci. 2024 Jun;27(6):1051-1063. doi: 10.1038/s41593-024-01616-4. Epub 2024 Apr 9.
10
Bento: a toolkit for subcellular analysis of spatial transcriptomics data.本托:用于空间转录组学数据分析的亚细胞分析工具包。
Genome Biol. 2024 Apr 2;25(1):82. doi: 10.1186/s13059-024-03217-7.
Nucleic Acids Res. 2017 Jan 4;45(D1):D626-D634. doi: 10.1093/nar/gkw1134. Epub 2016 Nov 29.
4
UniProt: the universal protein knowledgebase.通用蛋白质知识库:UniProt
Nucleic Acids Res. 2017 Jan 4;45(D1):D158-D169. doi: 10.1093/nar/gkw1099. Epub 2016 Nov 29.
5
The RCSB protein data bank: integrative view of protein, gene and 3D structural information.RCSB蛋白质数据库:蛋白质、基因与三维结构信息的综合视图。
Nucleic Acids Res. 2017 Jan 4;45(D1):D271-D281. doi: 10.1093/nar/gkw1000. Epub 2016 Oct 27.
6
Alternative Splicing May Not Be the Key to Proteome Complexity.可变剪接可能并非蛋白质组复杂性的关键所在。
Trends Biochem Sci. 2017 Feb;42(2):98-110. doi: 10.1016/j.tibs.2016.08.008. Epub 2016 Oct 3.
7
The Ensembl gene annotation system.Ensembl基因注释系统。
Database (Oxford). 2016 Jun 23;2016. doi: 10.1093/database/baw093. Print 2016.
8
The Pfam protein families database: towards a more sustainable future.Pfam蛋白质家族数据库:迈向更可持续的未来。
Nucleic Acids Res. 2016 Jan 4;44(D1):D279-85. doi: 10.1093/nar/gkv1344. Epub 2015 Dec 15.
9
Reference sequence (RefSeq) database at NCBI: current status, taxonomic expansion, and functional annotation.美国国立生物技术信息中心的参考序列(RefSeq)数据库:当前状态、分类扩展及功能注释。
Nucleic Acids Res. 2016 Jan 4;44(D1):D733-45. doi: 10.1093/nar/gkv1189. Epub 2015 Nov 8.
10
Functional Networks of Highest-Connected Splice Isoforms: From The Chromosome 17 Human Proteome Project.高连接性剪接异构体的功能网络:来自17号染色体人类蛋白质组计划
J Proteome Res. 2015 Sep 4;14(9):3484-91. doi: 10.1021/acs.jproteome.5b00494. Epub 2015 Aug 11.