• 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

具有医学遗传学和药物发现价值的人类加速基因组区域。

Human accelerated genome regions with value in medical genetics and drug discovery.

机构信息

Hubei Key Laboratory of Agricultural Bioinformatics, College of Informatics, Huazhong Agricultural University, Wuhan 430070, PR China.

Hubei Key Laboratory of Agricultural Bioinformatics, College of Informatics, Huazhong Agricultural University, Wuhan 430070, PR China.

出版信息

Drug Discov Today. 2020 May;25(5):821-827. doi: 10.1016/j.drudis.2020.03.001. Epub 2020 Mar 7.

DOI:10.1016/j.drudis.2020.03.001
PMID:32156545
Abstract

Accumulated evolutionary knowledge not only benefits our understanding of the pathogenesis of diseases, but also help in the search for new drug targets. This is further supported by the recent finding that human accelerated regions (HARs) identified by comparative genomic studies are linked to human neural system evolution and are also associated with neurological disorders. Here, we analyze the associations between HARs and diseases and drugs. We found that 32.42% of approved drugs target at least one HAR gene, which is higher than the ratio of in-research drugs. More interestingly, HAR gene-targeted drugs are most significantly enriched with agents treating neurological disorders. Thus, HAR genes have important implications in medical genetics and drug discovery.

摘要

积累的进化知识不仅有助于我们理解疾病的发病机制,还有助于寻找新的药物靶点。最近的研究发现,通过比较基因组研究确定的人类加速区域(HARs)与人类神经系统的进化有关,也与神经紊乱疾病有关,这进一步证实了这一点。在这里,我们分析了 HARs 与疾病和药物之间的关联。我们发现,32.42%的已批准药物至少针对一个 HAR 基因,这一比例高于在研药物。更有趣的是,HAR 基因靶向药物在治疗神经紊乱疾病的药物中最为显著。因此,HAR 基因在医学遗传学和药物发现中具有重要意义。

相似文献

1
Human accelerated genome regions with value in medical genetics and drug discovery.具有医学遗传学和药物发现价值的人类加速基因组区域。
Drug Discov Today. 2020 May;25(5):821-827. doi: 10.1016/j.drudis.2020.03.001. Epub 2020 Mar 7.
2
Can medical genetics and evolutionary biology inspire drug target identification?医学遗传学和进化生物学能否启发药物靶点的发现?
Trends Mol Med. 2012 Feb;18(2):69-71. doi: 10.1016/j.molmed.2011.11.004. Epub 2011 Dec 13.
3
Geneticists tap human knockouts.遗传学家利用人类基因敲除技术。
Nature. 2014 Oct 30;514(7524):548. doi: 10.1038/514548a.
4
[Genetics, genomics and medicine].[遗传学、基因组学与医学]
Presse Med. 2012 Jan;41(1):1-2. doi: 10.1016/j.lpm.2011.09.003. Epub 2011 Oct 12.
5
Human genomics in cardiovascular medicine: implications and perspectives.心血管医学中的人类基因组学:意义与展望。
Circ J. 2013;77(4):876-85. doi: 10.1253/circj.cj-13-0126. Epub 2013 Mar 8.
6
Using biointelligence to search the cancer genome: an epistemological perspective on knowledge recovery strategies to enable precision medical genomics.利用生物智能搜索癌症基因组:一种从认识论角度看待知识恢复策略,以实现精准医学基因组学。
Oncogene. 2008 Dec;27 Suppl 2:S58-66. doi: 10.1038/onc.2009.354.
7
Genomics moves into the clinic.基因组学走进临床。
Biotechniques. 2012 Feb;52(2):73-6. doi: 10.2144/000113806.
8
Mining drug-disease relationships as a complement to medical genetics-based drug repositioning: Where a recommendation system meets genome-wide association studies.挖掘药物-疾病关系,作为基于医学遗传学的药物再定位的补充:推荐系统与全基因组关联研究的结合。
Clin Pharmacol Ther. 2015 May;97(5):451-4. doi: 10.1002/cpt.82. Epub 2015 Apr 3.
9
Enhancer Function and Evolutionary Roles of Human Accelerated Regions.人类加速区的增强子功能和进化作用。
Annu Rev Genet. 2022 Nov 30;56:423-439. doi: 10.1146/annurev-genet-071819-103933. Epub 2022 Sep 7.
10
The gut microbiota links disease to human genome evolution.肠道微生物组将疾病与人类基因组进化联系起来。
Trends Genet. 2023 Jun;39(6):451-461. doi: 10.1016/j.tig.2023.02.006. Epub 2023 Mar 3.

引用本文的文献

1
Identification of Key Genes and Pathways Associated with Frailty and Exercise Effects Using a Network and Evolutionary Approach.使用网络和进化方法识别与衰弱及运动效果相关的关键基因和通路。
Genes (Basel). 2025 Aug 19;16(8):976. doi: 10.3390/genes16080976.
2
Spatial Transcriptomics: A Powerful Tool in Disease Understanding and Drug Discovery.空间转录组学:疾病理解和药物发现的有力工具。
Theranostics. 2024 May 11;14(7):2946-2968. doi: 10.7150/thno.95908. eCollection 2024.
3
Exploration of the Noncoding Genome for Human-Specific Therapeutic Targets-Recent Insights at Molecular and Cellular Level.
探索人类特异性治疗靶点的非编码基因组——分子和细胞水平的最新见解。
Cells. 2023 Nov 20;12(22):2660. doi: 10.3390/cells12222660.
4
Evolution-strengthened knowledge graph enables predicting the targetability and druggability of genes.进化增强知识图谱能够预测基因的可靶向性和成药性。
PNAS Nexus. 2023 Apr 26;2(5):pgad147. doi: 10.1093/pnasnexus/pgad147. eCollection 2023 May.
5
A Systematic Review of the Human Accelerated Regions in Schizophrenia and Related Disorders: Where the Evolutionary and Neurodevelopmental Hypotheses Converge.精神分裂症及相关障碍的人类加速区的系统综述:进化和神经发育假说的交汇点。
Int J Mol Sci. 2023 Feb 10;24(4):3597. doi: 10.3390/ijms24043597.
6
Identification of Key Genes and Pathways Associated with Preeclampsia by a WGCNA and an Evolutionary Approach.基于 WGCNA 和进化分析鉴定子痫前期相关的关键基因和通路。
Genes (Basel). 2022 Nov 17;13(11):2134. doi: 10.3390/genes13112134.
7
Enhancer Function and Evolutionary Roles of Human Accelerated Regions.人类加速区的增强子功能和进化作用。
Annu Rev Genet. 2022 Nov 30;56:423-439. doi: 10.1146/annurev-genet-071819-103933. Epub 2022 Sep 7.
8
Genetic variations in evolutionary accelerated regions disrupt cognition in schizophrenia.进化加速区的遗传变异破坏精神分裂症患者的认知。
Psychiatry Res. 2022 Aug;314:114586. doi: 10.1016/j.psychres.2022.114586. Epub 2022 May 13.
9
Revisiting Schizophrenia from an Evolutionary Perspective: An Association Study of Recent Evolutionary Markers and Schizophrenia.从进化角度重新审视精神分裂症:近期进化标记与精神分裂症的关联研究。
Schizophr Bull. 2021 Apr 29;47(3):827-836. doi: 10.1093/schbul/sbaa179.
10
Blood Cell DNA Methylation of Aging-Related Ubiquitination Gene Can Predict the Onset of Early Stage Colorectal Cancer.衰老相关泛素化基因的血细胞DNA甲基化可预测早期结直肠癌的发病
Front Oncol. 2020 Nov 27;10:544330. doi: 10.3389/fonc.2020.544330. eCollection 2020.